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Review

Osteonecrosis of the Jaws Associated with Herpes Zoster Infection: A Systematic Review and a Rare Case Report

by
Antonio Mancini
1,†,
Fabrizio Chirico
2,†,
Angelo Michele Inchingolo
1,
Fabio Piras
1,
Valeria Colonna
1,
Pierluigi Marotti
1,
Claudio Carone
1,
Alessio Danilo Inchingolo
1,
Francesco Inchingolo
1,* and
Gianna Dipalma
1
1
Department of Interdisciplinary Medicine, University of Bari “Aldo Moro”, 70124 Bari, Italy
2
U.O.C. Maxillofacial Surgery, University of Campania ‘Luigi Vanvitelli’, 81100 Caserta, Italy
*
Author to whom correspondence should be addressed.
These authors contributed equally as first authors.
Microorganisms 2024, 12(8), 1506; https://doi.org/10.3390/microorganisms12081506
Submission received: 2 July 2024 / Revised: 12 July 2024 / Accepted: 18 July 2024 / Published: 23 July 2024
(This article belongs to the Special Issue Human Infectious Diseases)

Abstract

:
The investigation’s goal was to obtain further knowledge about the connection between Herpes Zoster infection and dentistry therapy for the osteonecrosis of the jaws, combining the review with a case report relevant to the purpose. It is important to study this association because it is a possible additional factor to be considered in the causes of the osteonecrosis of the jaws. We limited our search to English-language papers published between 1 January 2004 and 7 June 2024 in PubMed, Scopus, and Web of Science that were relevant to our topic. In the search approach, the Boolean keywords “Herpes Zoster AND osteonecros*” were used. Results: This study analyzed 148 papers from Web of Science, PubMed, and Scopus, resulting in 95 articles after removing duplicates. Of these, 49 were removed because they were off topic, and 46 were confirmed. This study includes a qualitative analysis of the final 12 articles, removing 34 articles that were off topic. The literature highlights severe oral complications from Herpes Zoster reactivation, emphasizing the need for early diagnosis, comprehensive management, and multidisciplinary care. Treatment strategies include antiviral therapy, pain management, surgical debridement, and antibiotics. Immunocompromised individuals require vigilant monitoring and balanced immunosuppressive therapy. Further research is needed to enhance therapeutic approaches.

1. Introduction

Herpes simplex virus (HSV) infections are widespread, affecting a significant portion of the global population [1,2,3]. HSV is a DNA virus that is mostly divided into two types: HSV-1, which usually causes orolabial herpes, and HSV-2, which is more frequently the cause of genital herpes [4,5,6]. HSV is a member of the Herpesviridae family of viruses [7,8,9,10]. While HSV is primarily recognized for its mucocutaneous presentations, there has been a growing interest in recent years regarding its possible involvement in systemic disorders, such as osteonecrosis [11,12,13,14,15]. This distinction is important because, although they belong to the same family, the viruses generate diverse diseases and clinical manifestations. The focus on HSV draws attention to its increasing significance beyond conventional mucocutaneous symptoms and calls for more research into viral etiologies in systemic diseases like osteonecrosis.
Avascular necrosis, also known as osteonecrosis, is a medical condition where bone tissue dies from inadequate blood flow [16,17,18,19,20]. If left untreated, this illness can lead to severe functional disability, the collapse of the bones, and joint discomfort [21,22,23,24,25,26].
In the United States alone, the incidence of osteonecrosis is significant, with an estimated annual incidence ranging from 10,000 to 20,000 cases, and it is particularly common in individuals aged 30 to 50.
Osteonecrosis has an incidence rate ranging from approximately 1.4 to 3.0 per 100,000 person-years, with the hip being the most commonly diagnosed site, accounting for about 75.9% of cases. Significant risk factors include corticosteroid use, which triples the risk of osteonecrosis, and other conditions such as osteoporosis, cancer, and connective tissue diseases [27].
While direct associations between HSV and osteonecrosis are less frequently documented, a study revealed that viral infections, including those caused by herpesviruses, play a role in the non-traumatic etiology of osteonecrosis. Continued research is necessary to better understand the prevalence of HSV in osteonecrosis cases and its impact on bone health [28].
Osteonecrosis has a complicated and multifaceted etiology, with both traumatic and non-traumatic causes playing a role in its development [29,30,31,32]. Viral infections, especially those brought on by herpesviruses, are among the non-traumatic causes that have been linked to the pathophysiology of osteonecrosis [32,33,34,35,36]. Osteonecrosis and HSV infection are thought to be related by inflammatory reactions that cause vascular damage, direct viral cytopathic effects on bone cells, and autoimmune reactions that worsen the death of bone tissue [37,38,39,40,41]. Osteonecrosis may persist and progress longer if chronic, repeated episodes of HSV are allowed to establish latency and reawaken on a periodic basis [42,43,44,45].
Hospital admissions are significantly impacted by Herpes Zoster (HZ), often known as shingles. Research indicates that it may result in a significant number of hospital admissions, particularly in elderly and immunocompromised people. Hospitalizations associated to HZ have been found to rise with age, which is consistent with the virus’s increased prevalence in the elderly [46].
An Italian study, for example, found that HZ places a significant strain on hospital resources, with hospitalization rates among people 50 years of age and older being particularly high. This pattern highlights the high expense of healthcare and the necessity of efficient administration and preventative measures. Although the varicella vaccine has changed the epidemiology of HZ in the US, hospital admission rates have lately plateaued or even decreased, possibly as a result of increased vaccination rates and early therapeutic interventions [47].
The aforementioned data emphasize the vital necessity of continuous surveillance and public health campaigns to effectively control and alleviate the effects of HZ on healthcare systems across the globe.
The studies analyzed in this research underscore diverse RHS symptoms and stress early diagnosis, comprehensive care, and interdisciplinary treatment. Tailored therapies like surgery and antivirals are crucial for managing oral issues. Kaur, Cloarec, and Song addressed VZV challenges in HIV patients, advocating for vigilant monitoring, prompt intervention, and multidisciplinary care [48,49,50].
Several publications highlight significant oral complications from VZV reactivation in immunocompetent patients, emphasizing early identification and multidisciplinary management. Successful outcomes in VZV-related osteonecrosis hinge on surgical intervention, antibiotics, and tailored treatments, necessitating ongoing research and innovative approaches [17,18,51].
In this systematic analysis, we also describe a thorough case report: a unique instance of osteonecrosis that may have been caused by an infection with the herpes simplex virus. By outlining this patient’s clinical presentation, diagnostic process, and case management, we wish to raise awareness of the possible connection between HSV and osteonecrosis. This study emphasizes how crucial it is to take viral etiologies into account when treating individuals who have osteonecrosis that cannot be explained and recommends more investigation to determine how HSV functions in the pathophysiology of this crippling bone disease.
Our goals with this review and case report are to encourage medical professionals to perform comprehensive diagnostic evaluations for patients who present with osteonecrosis, especially if they have a history of recurrent herpesvirus infections, and to add to the growing body of research on the systemic effects of these infections.

2. Materials and Methods

2.1. Protocol and Registration

This review was carried out in accordance with PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines, and it was registered under the number CRD564003 on PROSPERO (The International Prospective Register of Systematic Reviews) [52]. In addition to the review, a case report of a patient with HZ associated with the clinical manifestation of osteonecrosis at the mandibular level was incorporated into the article.

2.2. Search Processing

We limited our search to English-language papers published between 1 January 2004 and 7 June 2024 in PubMed, Scopus, and Web of Science that were relevant to our topic. In the search approach, the Boolean keywords “Herpes Zoster AND osteonecros*” were used. We selected these phrases because they most accurately reflected our investigation’s aim, which was to gain additional insight into the interaction between HZ infection and dentistry therapy for the osteonecrosis of the jaws (Table 1).

2.3. Inclusion Criteria

Three reviewers evaluated all relevant papers based on the following chosen criteria: (1) solely human subjects in studies; (2) complete text; and (3) scientific studies evaluating the management of the removal of the osteonecrosis of the jaws. The following process was used to construct the PICO model:
  • Criteria: Application in the present study;
  • Population: Human subjects with the osteonecrosis of the jaws with HZ infection;
  • Intervention: Dentistry treatment for the removal of osteonecrosis;
  • Comparison: Control group;
  • Outcome: Evaluation of healing;
  • Study design: Case reports.

2.4. Exclusion Criteria

Articles written in languages other than English, ineligible study designs, ineligible outcome measures, ineligible populations, case studies, reviews, and animal studies were among the exclusion criteria.

2.5. Data Processing

Two reviewers (F.P. and V.C.) searched the database to extrapolate the studies and assessed their quality independently, according to selection criteria. During the screening phase, we excluded articles that did not fit the topic by reading the manuscript title and the abstract. The full texts of the remaining articles were read to conduct an eligibility analysis, according to the inclusion criteria. The selected articles were downloaded in Zotero (version 6.0.15). Any discrepancies between the two authors were resolved by consulting a senior reviewer (F.I.).

2.6. Article Identification Procedure

The appropriateness evaluation was performed independently by two reviewers, F.I. and F.P. An additional manual search was conducted to increase the number of articles available for full-text analysis. English-language articles that met the inclusion criteria were taken into consideration, and duplicates and items that did not qualify were marked with the reason that they were not included.

2.7. Study Evaluation

The article data were independently evaluated by the reviewers using a special electronic form designed according to the following categories: authors, year of study, aim of the study, materials and methods, and results.

2.8. Quality Assessment

Two reviewers, F.P. and F.I., evaluated the included papers’ quality using the ROBINS-I tool (Cochrane Bias Methods Group and the Cochrane Non-Randomised Studies of Interventions Methods Group—Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License). In order to evaluate the possibility of bias in the outcomes of non-randomized trials comparing the health impacts of two or more therapies, ROBINS-I was created. Each of the seven evaluated points was given a bias degree. F.I., the third reviewer, was consulted in the case of disagreement until a consensus was reached. The reviewers were instructed on how to use the ROBINS-I tool and adhered to the guidelines in order to assess the potential for bias in seven different domains: confounding, participant selection, intervention classification, deviations from intended interventions, missing data, outcome measurement, and choice of reported results. Discussion and consensus were used to settle any differences or conflicts amongst reviewers in order to improve the assessments’ objectivity and uniformity. In situations when agreement could not be reached, the final decision was made by a third reviewer. An extensive assessment of potential biases in the non-randomized studies included in this study was made possible by the use of ROBINS-E for bias assessment. This contributed to the overall evaluation of the caliber and dependability of the results by pointing out the evidence base’s advantages and disadvantages. The writers of this review were able to reach more informed interpretations and conclusions based on the facts at hand by taking the risk of bias into account.

3. Results

A total of 148 papers were obtained from the databases Web of Science (30), PubMed (32), and Scopus (86). This resulted in 95 articles after eliminating duplicates (53). Next, 49 entries were eliminated after their titles and abstracts were examined because they did not fit the inclusion criteria. The writers were able to successfully obtain the remaining 46 papers and confirm their eligibility; 34 items were eliminated as a result of this process because they were off topic. The qualitative analysis of the 12 final articles is included in this study (Figure 1). Each study’s findings are presented in Table 2.

Quality Assessment and the Risk of Bias in the Included Articles

The risk of bias in the included studies is reported in Figure 2. Regarding the bias due to confounding, most studies had some concerns. The bias arising from measurement is a parameter with low risk of bias. Many studies had low risk of bias due to bias in selection of participants. Bias due to post exposure could not be calculated due to high heterogeneity. The bias due to missing data was low in many studies. Bias arising from measurement of the outcome was low. Bias in the selection of the reported results was low in most studies. The final results show that one study had a high risk of bias, four had a very high risk of bias, and four had a low risk of bias.

4. Discussion

HZ, commonly known as shingles, is caused by the reactivation of the varicella zoster virus (VZV), which lies dormant in the dorsal root ganglia after an initial chickenpox infection [60,61,62,63,64]. This viral reactivation can lead to various complications, particularly when the trigeminal nerve is involved, potentially resulting in severe oral health issues [65,66,67,68,69]. Osteonecrosis, or the death of bone tissue, is a particularly concerning complication of HZ, often manifesting in the maxillofacial region and leading to significant morbidity [70,71,72]. This paper explores the incidence and management of HZ–related osteonecrosis across different patient populations, including those with Ramsay Hunt Syndrome (RHS), AIDS, and generally healthy individuals [73,74,75,76].

4.1. Patients with Ramsay Hunt Syndrome

Ramsay Hunt Syndrome (RHS) is a severe neurological condition resulting from the reactivation of the VZV within the trigeminal nerve ganglia [77,78,79,80,81]. It affects adults, particularly those over 60 (about 5 out of every 100,000 people each year), and is primarily caused by impaired immune systems and stress. The incidence is significant, with a higher rate among the elderly population. This reactivation can lead to a range of complications, including osteonecrosis and tooth exfoliation. The cases presented by Garima Singh et al., Maojia Yin et al., Travis Rudd et al., and Samprati J. Badjate et al. provide insight into the diverse manifestations and management strategies for RHS [82,83,84,85]. Garima Singh et al. reported a case involving a 13-year-old girl who developed alveolar osteonecrosis and subsequent tooth loss following VZV infection [56,86,87]. This case highlights the significant risk of these complications even in younger patients and underscores the critical need for early diagnosis and comprehensive management. The young age of the patient emphasizes the importance of maintaining a high index of suspicion for VZV-related oral complications across all age groups [88,89]. In contrast, Maojia Yin et al. described a 50-year-old man with RHS characterized by severe facial and mandibular pain, rapid tooth loss, and mild facial paralysis [18,90,91]. The treatment involved a tailored regimen including gabapentin, pregabalin, paracetamol–tramadol, and eperisone hydrochloride, supplemented by periodic debridement of necrotic bone and prophylactic antibiotics [92,93,94,95]. This multidisciplinary approach was crucial in managing pain and controlling the progression of osteonecrosis, highlighting the necessity of individualized treatment strategies for RHS patients [96,97,98,99,100]. Travis Rudd et al. documented a case of a 59-year-old man with granulomatosis with polyangiitis who developed severe mandibular osteonecrosis and RHS subsequent to VZV reactivation [59,101,102]. Despite aggressive treatment with intravenous antivirals and surgical debridement, the patient experienced persistent symptoms, underscoring the chronic nature of RHS-associated complications [103,104,105,106]. This case highlights the importance of vigilant long-term follow-up and continuous interdisciplinary care in managing complex RHS scenarios effectively [107,108,109,110]. Samprati J. Badjate et al. presented an 86-year-old male with RHS, post-herpetic neuralgia, and bilateral osteonecrosis involving both the maxilla and mandible [17,111]. The treatment comprised initial antiviral therapy followed by surgical debridement and antibiotic administration, resulting in favorable wound-healing outcomes [112,113,114]. This case emphasizes the pivotal role of timely intervention and a collaborative medical approach in mitigating severe VZV-related complications in the craniofacial region [115,116,117]. In summary, the cases presented by Garima Singh et al., Maojia Yin et al., Travis Rudd et al., and Samprati J. Badjate et al. [17,18,53,56] highlight the diverse manifestations of RHS and the importance of early diagnosis, comprehensive management, and multidisciplinary care. The varying ages of the patients and the severity of their symptoms underscore the need for tailored treatment strategies and vigilant long-term follow-up [118,119]. These cases also emphasize the critical role of antiviral therapy, surgical debridement, and antibiotic administration in managing the oral and maxillofacial complications of RHS.

4.2. Patients with AIDS

Individuals with AIDS exhibit a significantly elevated incidence of VZV reactivation due to immunosuppression [120,121]. Rupinder Kaur emphasized that, while VZV prevalence in the general population is 5.4%, it can be up to 10 times higher in HIV-positive individuals [48,122,123,124,125]. This heightened susceptibility underscores the critical need for vigilant monitoring and prompt intervention in this vulnerable patient cohort [126,127,128,129]. Nicolas Cloarec discussed the administration of azathioprine in HIV-infected patients under highly active antiretroviral therapy (HAART), noting its safe usage with close immunological monitoring [49]. However, he cautioned about potential adverse effects, including complications from VZV reactivation, emphasizing the delicate balance required in managing immunosuppressive therapies in HIV/AIDS patients [130,131,132]. Furthermore, Jae-Min Song’s literature review highlighted severe oral manifestations of VZV infection in immunocompromised patients, such as those with HIV/AIDS [50]. Involvement of the trigeminal nerve branches can lead to complications such as acute pulpitis, dental pain, root resorption, and periapical lesions, necessitating immediate antiviral treatment and effective pain management strategies to mitigate the risk of post-herpetic neuralgia and further oral deterioration [133,134,135]. In summary, the discussions by Rupinder Kaur, Nicolas Cloarec, and Jae-Min Song highlight the unique challenges posed by VZV reactivation in HIV-positive individuals. The elevated incidence of VZV infection in this population necessitates vigilant monitoring and prompt intervention [83,106,136,137,138]. The use of immunosuppressive therapies, such as azathioprine, requires careful management to balance the benefits and risks, including the potential for VZV reactivation. Additionally, the severe oral manifestations of VZV infection in immunocompromised patients underscore the need for immediate antiviral treatment and effective pain management strategies to prevent further complications. These findings emphasize the importance of a multidisciplinary approach in managing VZV-related complications in HIV/AIDS patients [139,140,141].

4.3. Healthy Patients or Those without Either Pathology

Even in immunocompetent individuals, VZV reactivation can result in significant oral complications, albeit less frequently and severely compared to immunocompromised patients [142,143,144,145]. Garima Singh et al. noted that, while VZV primarily affects older adults, cases like that of the young girl underscore the importance of maintaining a high index of suspicion for VZV-related oral complications across all age groups [146,147,148,149]. C. Mendieta’s research further explored the prevalence of VZV in the general population and its potential to cause neuralgia and oral lesions [57,150,151,152,153]. This study highlighted that trigeminal nerve involvement can lead to substantial oral health issues such as tooth loss due to alveolar bone necrosis, emphasizing the need for early diagnosis and comprehensive management strategies in healthy individuals [154,155,156,157]. Emilie Faure et al. described an 87-year-old man with uncontrolled diabetes who developed mandibular osteonecrosis following VZV infection [51]. Despite his compromised health status, the patient’s condition was successfully managed through surgical resection of necrotic bone and antibiotic therapy, underscoring the importance of addressing underlying health conditions to optimize recovery [110,158,159,160]. Kaikai Huang et al. discussed rare but severe complications of alveolar osteonecrosis associated with VZV, stressing the critical need for awareness and prompt treatment to mitigate oral and maxillofacial complications [54]. This review emphasized the necessity for further research into pathogenesis and treatment strategies for VZV-related osteonecrosis [161,162,163,164]. Aritra Chatterjee et al. presented a unique case of the osteonecrosis of the jaw (ONJ) following VZV infection in a 51-year-old man [55,165,166]. Despite initial symptomatic treatment, the patient developed spontaneous tooth exfoliation and mandibular bone necrosis, necessitating surgical intervention and antibiotic therapy [167,168,169]. This case underscores the complexity of managing postherpetic ONJ and the importance of tailored treatment approaches. Kamala G. Pillai highlighted that VZV can affect cranial nerves, particularly the trigeminal nerve, potentially leading to osteomyelitis and spontaneous tooth loss [14,170,171,172]. Her review of cases illustrated rapid disease progression and severe bone destruction, emphasizing the need for preventive measures and early intervention to mitigate these risks [49,173,174,175]. In summary, the discussions by Garima Singh et al., C. Mendieta, Emilie Faure et al., Kaikai Huang et al., Aritra Chatterjee et al., and Kamala G. Pillai highlight the significant oral complications that can arise from VZV reactivation in immunocompetent individuals [76,176,177,178]. These complications, ranging from alveolar bone necrosis to osteomyelitis and tooth loss, underscore the importance of early diagnosis and comprehensive management strategies [179,180,181,182]. The successful management of these cases through surgical intervention, antibiotic therapy, and tailored treatment approaches emphasizes the need for a multidisciplinary approach [183,184,185,186]. Additionally, the review by Kaikai Huang et al. highlights the necessity for further research into the pathogenesis and treatment strategies for VZV-related osteonecrosis, emphasizing the ongoing need for vigilance and innovative therapeutic approaches in managing these complex conditions [187,188,189,190,191]. In conclusion, the discussed literature underscores the critical importance of early diagnosis, comprehensive treatment, and multidisciplinary care in managing VZV-related complications across diverse patient populations [192,193,194,195]. Whether in the context of RHS, HIV/AIDS, or healthy individuals, understanding the distinct challenges and tailoring treatment accordingly are crucial for optimizing patient outcomes [196,197,198,199,200,201].

4.4. Analysis of Lack of Vaccine

There are a number of reasons why patients with problems from HZ may not have had a vaccine, including the following:
  • Access and Availability: Depending on factors like cost, availability, or healthcare infrastructure, certain areas may not have easy access to vaccinations;
  • Vaccine hesitation: Undervaccination can result from vaccine hesitation caused by false information, cultural values, or personal convictions;
  • Immunocompetence: Certain people may not be able to receive vaccinations or may respond less well to them, especially if they have an immunocompromising medical problem;
  • Age-Related Factors: Adults above a particular age should receive the shingles vaccine; however, undervaccination in that age group might occur from a lack of knowledge or availability.
The VZV vaccination has the potential to significantly lower the frequency and severity of HZ and its associated consequences, such as osteonecrosis [202,203,204]. The possible effects of vaccination are highlighted by the following points:
  • Prevention of Initial Infection
Childhood vaccination against varicella, or chickenpox, helps avoid the virus’s first infection, lowering the possibility that it will lie dormant and reactivate as HZ later in life. Immunocompetent people should pay special attention to this as it can drastically lower the general prevalence of HZ in the community;
2.
Reduction of HZ Incidence in Adults
By increasing the immune response to VZV, the shingles vaccine, which is advised for individuals over a specific age, can lower the risk of HZ. Due to the age-related reduction in immune function, older persons are particularly benefiting from this, since they are more likely to acquire HZ and its associated consequences;
3.
Mitigation of Complications in Immunocompromised Individuals
Immunocompromised people, such as those with AIDS, may benefit less from vaccination, although it can still provide some protection against VZV reactivation and its consequences. In these situations, it is crucial to carefully weigh the patient’s immunological condition as well as the possible advantages and disadvantages of vaccination;
4.
Public Health Implications
Reducing the burden of problems connected to HZ can be achieved in part by addressing vaccine reluctance, expanding immunization rates through public health initiatives, and enhancing vaccine accessibility. Part of this involves spreading knowledge about the existence of the shingles and chickenpox vaccinations as well as their significance in avoiding HZ and its severe symptoms [205,206,207,208,209].
To sum up, immunization against VZV is an essential part of the plan to lower the frequency and severity of HZ and its side effects, such as osteonecrosis. Public health authorities and healthcare personnel may greatly enhance patient outcomes for a wide range of groups by advocating for children and adult vaccinations.

4.5. Study Limitations

It is important to recognize the following limitations while studying and analyzing HZ and its associated consequences, especially osteonecrosis, in a variety of patient groups, including those with AIDS, RHS, and normally healthy people:
  • Sample Size and Representativeness: The cases that are being reviewed are drawn from short case series and individual patient reports. This restricts the findings’ applicability to a larger population. To completely comprehend the incidence and prevalence of HZ-related osteonecrosis across various patient categories, larger, more representative investigations are required;
  • Selection Bias: Not all patients with HZ or RHS may be represented by the instances that are provided. The perception of the normal presentation and severity of problems connected to HZ may be skewed to a potential bias towards reporting instances that are more severe or uncommon;
  • Absence of Longitudinal Data: Long-term follow-up data are lacking in many of the examples that are described. Because of this, evaluating the long-term effects and efficacy of different treatment approaches over time becomes difficult. To fully comprehend the chronic nature of issues connected to HZ and the long-term effects of therapy, longitudinal studies are required;
  • Variability in Treatment Options: As a reflection of the customized character of care, the treatment options presented differ greatly between instances. Nevertheless, it is challenging to obtain firm judgments regarding the best course of action in terms of therapy. This issue may be addressed with the use of comparative research and standardized treatment methods;
  • Variability in Treatment Choices: The treatment choices offered vary significantly between cases, reflecting the individualized nature of therapy. However, it might be difficult to obtain definitive opinions about the optimal therapeutic approach. Standardized treatment techniques and comparative studies may be used to solve this problem;
  • Immunocompetence Variability: Patients’ immune systems can differ significantly, even within those in the same diagnostic group (AIDS and RHS, as examples). The manifestation and seriousness of issues linked to HZ can be influenced by this variability. Research that takes into consideration and evaluates the effects of varying degrees of immunocompetence is required;
  • Geographic and Demographic Variability: It is possible that the examples examined do not accurately reflect populations throughout the world. The frequency, manifestation, and consequences of HZ can be influenced by demographic and geographic variables. More extensive global research may yield more thorough understanding;
  • Emerging Therapies and Research: As novel treatments and interventions are being investigated, the area of HZ and VZV-related problems is changing quickly. The necessity for ongoing updates to knowledge and treatment standards is highlighted by the possibility that the current conversation may not completely capture the most recent breakthroughs.

4.6. Clinical Implications

  • Early Diagnosis and Management
The instances discussed highlight how crucial it is to identify issues linked to HZ early on and to handle them comprehensively. Across all age ranges and patient demographics, healthcare personnel should keep a high index of suspicion for oral problems connected to VZV. For optimal therapy, multidisciplinary care, including oral surgeons, dentists, infectious disease specialists, and pain management experts, is essential;
2.
Tailored Treatment Strategies
Personalized treatment regimens are required because of the wide range in severity and manifestation of problems linked to HZ. These include the application of antibiotics, surgical debridement, antiviral treatment, and pain control techniques. Vigilant observation and timely action are crucial for patients with impaired immune systems, including those suffering from AIDS, in order to reduce the likelihood of serious consequences;
3.
Vaccination
The study emphasizes how crucial it is to get vaccinated against VZV. Both the adult shingles vaccine and the childhood chickenpox immunization can dramatically lower the frequency and seriousness of problems connected to HPZ. The main goals of public health initiatives should be to combat vaccine hesitancy, improve vaccine accessibility, and raise immunization rates via education;
4.
Long-Term Follow-Up
Because certain HZ-related consequences are chronic in nature, especially in complicated cases like RHS, ongoing multidisciplinary treatment and long-term follow-up are required to manage enduring symptoms and avert further problems.

4.7. Future Prospects

  • Research on Pathogenesis and Treatment
More investigation is required to improve our understanding of the pathophysiology of osteonecrosis linked to VZV and to create more potent treatment plans. This involves looking into the processes that lead to nerve involvement and bone loss. To determine standardized treatment procedures and assess the effectiveness of various treatment modalities, clinical trials and comparison studies are necessary;
2.
Innovative Therapeutic Approaches
Potential approaches to treating HZ-related problems include the creation of novel therapeutic agents and interventions, such as tailored antiviral treatments and regenerative medicine methods. Investigating the possibilities of stem cell therapy and tissue engineering as treatments for osteonecrosis may yield novel approaches;
3.
Vaccine Development
It is critical to continue ongoing research on vaccine development, particularly studies on the safety and effectiveness of vaccinations in immunocompromised populations. Investigating the possibilities of novel vaccine formulations and delivery systems is part of this;
4.
Global Health Perspectives
More extensive worldwide research is required to comprehend the occurrence and manifestation of HZ-related complications worldwide. This will support the creation of thorough global health policies and standards;
5.
Technological Advancements
The early diagnosis and monitoring of problems connected to HZ may be enhanced by the use of sophisticated diagnostic methods, such as imaging technology and biomarkers. Digital health platforms and telemedicine might improve access to care and help with the better management of long-term illnesses like RHS [210,211].
The reviewed literature offers strong proof that VZV infection is relevant to the onset of osteonecrosis. The need for early diagnosis, comprehensive management, and multidisciplinary care is highlighted by the numerous presentations and severe complications observed in different patient categories, such as patients with AIDS, RHS, and healthy persons. The prevention of VZV-related problems is mostly dependent on vaccination, and continued research is necessary to create more potent vaccines and treatment plans [212,213].

4.8. Case Presentation

A 74-year-old male patient visited the Department of Interdisciplinary Medicine, University of Bari “Aldo Moro”, on 31 January 2018, and his chief complaint was alveolar bone exposure of the right mandible. The patient received dental extractions from the right half of his jaw for destructive caries in the years preceding the onset of osteonecrosis. He presented absence of current pharmacological therapies and absence of current or previous pathologies, both systemic and in the head and neck area. He had an onset of herpetic rashes in the right side of the hemimandibula, concomitant with an area of bone exposure in the right side of the haemimandibula, which persisted after the resolution of skin symptoms (Figure 3A). He had no other relevant medical history. Intraoral examination showed alveolar bone exposure in the #43, #44 area (Figure 3B).
Radiographic examination, according to axial thin-layer scans (1 mm), reconstructed in coronal (panorex) and sagittal oblique planes (cross), showed calcium tone alteration with diffuse rarefaction of the bony trabeculae, with tissue swelling seen on computed tomography (Figure 4).
CT findings could be suggestive of ONJ; however, completion of a clinical–anamnestic–instrumental link is required. The patient had no history of receiving a prescription for any medication that affects bone metabolism and had never received radiotherapy. We determined that the inflammation originated from the patients’ teeth; thus, we diagnosed his condition as right mandibular osteonecrosis by trigeminal HZ. We treated him with sequestrectomy, and we removed teeth #31-#41-#42 (Figure 5).
After the surgery, a piece consisting of fragments of necrotic bone and inflammatory fibrous tissue was examined. According to histopathology, we observed clumps of necrotic material, fibroconnectival frustules with chronic non-specific inflammatory infiltration, and spicules of bone tissue, partly necrotic, surrounded by fibroconnectival vallo. There was an absence of post-operative complications and any osteogenesis of the area of previous osteonecrosis following resective surgery of the lesion itself. No additional tooth loss, bone exposure, or osteonecrosis occurred during the follow-up period. Also, no other complications, such as postherpetic neuralgia, occurred (Figure 6).

5. Conclusions

The reviewed literature and case study highlight the severe oral complications, particularly osteonecrosis, that can arise from HZ reactivation, emphasizing the necessity for early diagnosis, comprehensive management, and multidisciplinary care. In Ramsay Hunt Syndrome (RHS) patients, individualized treatment strategies involving antiviral therapy, pain management, surgical debridement, and antibiotics are crucial. Immunocompromised individuals, especially those with AIDS, require vigilant monitoring and a balanced approach to immunosuppressive therapy to prevent severe oral manifestations. Even immunocompetent individuals can experience significant complications, underscoring the need for a high index of suspicion and timely intervention. The 74-year-old male case reinforces the importance of thorough diagnostics and prompt surgical intervention for successful outcomes. Overall, tailored treatment, early diagnosis, and multidisciplinary care are vital for managing the complex complications of HZ, with further research needed to enhance therapeutic approaches.

Author Contributions

Conceptualization, A.M. and F.C.; methodology, A.M.I. and C.C.; software, V.C.; validation, V.C., P.M. and C.C.; formal analysis, A.D.I. and P.M.; investigation, F.I. and F.P.; resources, G.D.; data curation, F.I.; writing—original draft preparation, G.D.; writing—review and editing, F.P.; visualization, A.D.I.; supervision, A.M.I.; project administration, F.C.; funding acquisition, A.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The present clinical study was based at the University of Bari (Italy), in full accordance with ethical principles, including the World Medical Association Declaration of Helsinki and the additional requirements of Italian law. Furthermore, the University of Bari, Italy, classified the study to be exempt from ethical review, as it carried only negligible risk and involved the use of existing data that contained only non-identifiable data about human beings. The patient in the case study signed a written informed consent form.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

HAARTHighly active antiretroviral therapy
HSVHerpes simplex virus
HZIHerpes Zoster infection
IOMAIntegrative omics-metabolic analysis
ONJOsteonecrosis of the jaw
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
PROSPEROThe International Prospective Register of Systematic Reviews
RHSRamsey Hunt Syndrome
VZVVaricella zoster virus

References

  1. Schwartz, O.; Kvorning, S.A. Tooth Exfoliation, Osteonecrosis of the Jaw and Neuralgia Following Herpes Zoster of the Trigeminal Nerve. Int. J. Oral. Surg. 1982, 11, 364–371. [Google Scholar] [CrossRef] [PubMed]
  2. Laufer, J.; Tsamis, J.D. Zoster ophthalmicus: A problem in general practice (author’s transl). Rev. Stomatol. Chir. Maxillofac. 1979, 80, 239–241. [Google Scholar] [PubMed]
  3. Manz, H.J.; Canter, H.G.; Melton, J. Trigeminal Herpes Zoster Causing Mandibular Osteonecrosis and Spontaneous Tooth Exfoliation. South. Med. J. 1986, 79, 1026–1028. [Google Scholar] [CrossRef]
  4. Cooper, J.C. Tooth Exfoliation and Osteonecrosis of the Jaw Following Herpes Zoster. Br. Dent. J. 1977, 143, 297–300. [Google Scholar] [CrossRef] [PubMed]
  5. Volvoikar, P.; Patil, S.; Dinkar, A. Tooth Exfoliation, Osteonecrosis and Neuralgia Following Herpes Zoster of Trigeminal Nerve. Indian. J. Dent. Res. 2002, 13, 11–14. [Google Scholar] [PubMed]
  6. Garty, B.Z.; Dinari, G.; Sarnat, H.; Cohen, S.; Nitzan, M. Tooth Exfoliation and Osteonecrosis of the Maxilla after Trigeminal Herpes Zoster. J. Pediatr. 1985, 106, 71–73. [Google Scholar] [CrossRef] [PubMed]
  7. Jain, M.K.; Manjunath, K.S.; Jagadish, S.N. Unusual Oral Complications of Herpes Zoster Infection: Report of a Case and Review of Literature. Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. Endod. 2010, 110, e37–e41. [Google Scholar] [CrossRef] [PubMed]
  8. Eversole, L.R. Viral Infections of the Head and Neck among HIV-Seropositive Patients. Oral Surg. Oral Med. Oral Pathol. 2005, 73, 155–163. [Google Scholar] [CrossRef]
  9. Balasubramaniam, R.; Kuperstein, A.S.; Stoopler, E.T. Update on Oral Herpes Virus Infections. Dent. Clin. N. Am. 2014, 58, 265–280. [Google Scholar] [CrossRef] [PubMed]
  10. Steiner, I.; Benninger, F. Update on Herpes Virus Infections of the Nervous System. Curr. Neurol. Neurosci. Rep. 2013, 13, 414. [Google Scholar] [CrossRef]
  11. Khullar, S.M.; Tvedt, D.; Chapman, K.; Herlofson, B.B. Sixty Cases of Extreme Osteonecrosis and Osteomyelitis of the Mandible and Maxilla in a West African Population. Int. J. Oral. Maxillofac. Surg. 2012, 41, 978–985. [Google Scholar] [CrossRef] [PubMed]
  12. Muto, T.; Tsuchiya, H.; Sato, K.; Kanazawa, M. Tooth Exfoliation and Necrosis of the Mandible--a Rare Complication Following Trigeminal Herpes Zoster: Report of a Case. J. Oral. Maxillofac. Surg. 1990, 48, 1000–1003. [Google Scholar] [CrossRef] [PubMed]
  13. Tseng, H.F.; Bruxvoort, K.; Ackerson, B.; Luo, Y.; Tanenbaum, H.; Tian, Y.; Zheng, C.; Cheung, B.; Patterson, B.J.; Van Oorschot, D.; et al. The Epidemiology of Herpes Zoster in Immunocompetent, Unvaccinated Adults ≥50 Years Old: Incidence, Complications, Hospitalization, Mortality, and Recurrence. J. Infect. Dis. 2020, 222, 798–806. [Google Scholar] [CrossRef] [PubMed]
  14. Pillai, K.G.; Nayar, K.; Rawal, Y.B. Spontaneous Tooth Exfoliation, Maxillary Osteomyelitis and Facial Scarring Following Trigeminal Herpes Zoster Infection. Prim. Dent. Care 2006, 13, 114–116. [Google Scholar] [CrossRef] [PubMed]
  15. Mostofi, R.; Marchmont-Robinson, H.; Freije, S. Spontaneous Tooth Exfoliation and Osteonecrosis Following a Herpes Zoster Infection of the Fifth Cranial Nerve. J. Oral. Maxillofac. Surg. 1987, 45, 264–266. [Google Scholar] [CrossRef] [PubMed]
  16. Closmann, J.J.; Fielding, C.G.; Pogrel, M.A. Prevention and Management of Trigeminal Herpes Zoster and Postherpetic Neuralgia. Gen. Dent. 2008, 56, 563–566; quiz 567–568, 591–592. [Google Scholar] [PubMed]
  17. Badjate, S.J.; Cariappa, K.M.; Shenoi, S.R.; Nakhate, S. Ramsay-Hunt Syndrome Complicating Osteonecrosis of Edentulous Maxilla and Mandible: Report of a Rare Case. J. Maxillofac. Oral. Surg. 2009, 8, 188–191. [Google Scholar] [CrossRef]
  18. Yin, M.; Huang, P.; Yang, S.; Wang, W. Ramsay Hunt Syndrome and Mandibular Alveolar Bone Necrosis Following Herpes Zoster: A Case Report and Literature Review. Front. Neurol. 2022, 13, 1073607. [Google Scholar] [CrossRef] [PubMed]
  19. Shah, R.J.; Katyayan, M.K.; Katyayan, P.A.; Chauhan, V. Prosthetic Rehabilitation of Acquired Maxillary Defects Secondary to Mucormycosis: Clinical Cases. J. Contemp. Dent. Pract. 2014, 15, 242–249. [Google Scholar] [CrossRef]
  20. Slade, H.B.; Owens, M.L.; Tomai, M.A.; Miller, R.L. Imiquimod 5% Cream (Aldara). Expert. Opin. Investig. Drugs 1998, 7, 437–449. [Google Scholar] [CrossRef]
  21. Silva Santos, I.; Saueressig, F.; Pola, N.M.; Vasconcelos, A.C.U.; Rados, P.V.; Gomes, A.P.N.; Flores, I.L. Osteonecrosis of the Jaw as a Late Complication of Herpes Zoster Infection: A Case Report. Gen. Dent. 2020, 68, 36–39. [Google Scholar] [PubMed]
  22. Watson, C.P.N.; Deck, J.H.; Morshead, C.; Van der Kooy, D.; Evans, R.J. Post-Herpetic Neuralgia: Further Post-Mortem Studies of Cases with and without Pain. Pain. 1991, 44, 105–117. [Google Scholar] [CrossRef] [PubMed]
  23. Kalhori, K.A.M.; Vahdatinia, F.; Jamalpour, M.R.; Vescovi, P.; Fornaini, C.; Merigo, E.; Fekrazad, R. Photobiomodulation in Oral Medicine. Photobiomodul Photomed. Laser Surg. 2019, 37, 837–861. [Google Scholar] [CrossRef] [PubMed]
  24. Stefanov, G.; Beleva, B. Our experience with the dispensary observation and treatment of kidney transplant patients. Vut. Boles. 1981, 20, 34–39. [Google Scholar]
  25. Borsani, E.; Bonazza, V.; Buffoli, B.; Nocini, P.F.; Albanese, M.; Zotti, F.; Inchingolo, F.; Rezzani, R.; Rodella, L.F. Beneficial Effects of Concentrated Growth Factors and Resveratrol on Human Osteoblasts In Vitro Treated with Bisphosphonates. Biomed. Res. Int. 2018, 2018, 4597321. [Google Scholar] [CrossRef]
  26. Inchingolo, F.; Cantore, S.; Dipalma, G.; Georgakopoulos, I.; Almasri, M.; Gheno, E.; Motta, A.; Marrelli, M.; Farronato, D.; Ballini, A.; et al. Platelet Rich Fibrin in the Management of Medication-Related Osteonecrosis of the Jaw: A Clinical and Histopathological Evaluation. J. Biol. Regul. Homeost. Agents 2017, 31, 811–816. [Google Scholar]
  27. Lambade, P.; Lambade, D.; Saha, T.K.; Dolas, R.S.; Pandilwar, P.K. Maxillary Osteonecrosis and Spontaneous Teeth Exfoliation Following Herpes Zoster. Oral. Maxillofac. Surg. 2012, 16, 369–372. [Google Scholar] [CrossRef] [PubMed]
  28. Lin, J.R.; Huang, C.C. Oral complications following a herpes zoster infection of trigeminal nerve. Chang Yi Xue Za Zhi 1993, 16, 75–80. [Google Scholar]
  29. Hall, H.D.; Jacobs, J.S.; O’Malley, J.P. Necrosis of Maxilla in Patient with Herpes Zoster: Report of a Case. Oral. Surg. Oral. Med. Oral. Pathol. 1974, 37, 657–662. [Google Scholar] [CrossRef]
  30. Depledge, D.P.; Sadaoka, T.; Ouwendijk, W.J.D. Molecular Aspects of Varicella-Zoster Virus Latency. Viruses 2018, 10, 349. [Google Scholar] [CrossRef]
  31. Mintz, S.M.; Anavi, Y. Maxillary Osteomyelitis and Spontaneous Tooth Exfoliation after Herpes Zoster. Oral. Surg. Oral. Med. Oral. Pathol. 1992, 73, 664–666. [Google Scholar] [CrossRef] [PubMed]
  32. Pogrel, M.A.; Miller, C.E. A Case of Maxillary Necrosis. J. Oral. Maxillofac. Surg. 2003, 61, 489–493. [Google Scholar] [CrossRef]
  33. Gilbert, J.; Drehs, M.M.; Weinberg, J.M. Topical Imiquimod for Acyclovir-Unresponsive Herpes Simplex Virus 2 Infection. Arch. Dermatol. 2001, 137, 1015–1017. [Google Scholar] [PubMed]
  34. Schacker, T.W.; Conant, M.; Thoming, C.; Stanczak, T.; Wang, Z.; Smith, M. Imiquimod 5-Percent Cream Does Not Alter the Natural History of Recurrent Herpes Genitalis: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study. Antimicrob. Agents Chemother. 2002, 46, 3243–3248. [Google Scholar] [CrossRef] [PubMed]
  35. McKenzie, C.D.; Gobetti, J.P. Diagnosis and Treatment of Orofacial Herpes Zoster: Report of Cases. J. Am. Dent. Assoc. 1990, 120, 679–681. [Google Scholar] [CrossRef] [PubMed]
  36. Matsui, T.; Maruyama, F.; Miyazaki, H.; Nomura, T.; Ezaki, K.; Hirano, M.; Mizoguchi, Y. Disseminated varicella-zoster virus infection without vesicles in a patient with malignant lymphoma. Rinsho Ketsueki 1992, 33, 483–487. [Google Scholar] [PubMed]
  37. Chakrabarty, A.; Pang, K.R.; Wu, J.J.; Narvaez, J.; Rauser, M.; Huang, D.B.; Beutner, K.R.; Tyring, S.K. Emerging Therapies for Herpes Viral Infections (Types 1–8). Expert. Opin. Emerg. Drugs 2004, 9, 237–256. [Google Scholar] [CrossRef] [PubMed]
  38. Crute, J.J.; Grygon, C.A.; Hargrave, K.D.; Simoneau, B.; Faucher, A.-M.; Bolger, G.; Kibler, P.; Liuzzi, M.; Cordingley, M.G. Herpes Simplex Virus Helicase-Primase Inhibitors Are Active in Animal Models of Human Disease. Nat. Med. 2002, 8, 386–391. [Google Scholar] [CrossRef] [PubMed]
  39. Dipalma, G.; Inchingolo, A.D.; Piras, F.; Palmieri, G.; Pede, C.D.; Ciocia, A.M.; Siciliani, R.A.; Olio, F.D.; Inchingolo, A.M.; Palermo, A.; et al. Efficacy of Guided Autofluorescence Laser Therapy in MRONJ: A Systematic Review. Eur. Rev. Med. Pharmacol. Sci. 2023, 27, 11817–11831. [Google Scholar] [CrossRef]
  40. Kennedy, P.G.E.; Rovnak, J.; Badani, H.; Cohrs, R.J. A Comparison of Herpes Simplex Virus Type 1 and Varicella-Zoster Virus Latency and Reactivation. J. Gen. Virol. 2015, 96, 1581–1602. [Google Scholar] [CrossRef]
  41. van Heerden, W.F.; McEachen, S.E.; Boy, S.C. Alveolar Bone Necrosis and Tooth Exfoliation Secondary to Herpes Zoster in the Setting of HIV/AIDS. AIDS 2005, 19, 2183–2184. [Google Scholar] [CrossRef] [PubMed]
  42. Wright, W.E.; Davis, M.L.; Geffen, D.B.; Martin, S.E.; Nelson, M.J.; Straus, S.E. Alveolar Bone Necrosis and Tooth Loss: A Rare Complication Associated with Herpes Zoster Infection of the Fifth Cranial Nerve. Oral. Surg. Oral. Med. Oral. Pathol. 1983, 56, 39–46. [Google Scholar] [CrossRef] [PubMed]
  43. Contaldo, M.; Luzzi, V.; Ierardo, G.; Raimondo, E.; Boccellino, M.; Ferati, K.; Bexheti-Ferati, A.; Inchingolo, F.; Di Domenico, M.; Serpico, R.; et al. Bisphosphonate-Related Osteonecrosis of the Jaws and Dental Surgery Procedures in Children and Young People with Osteogenesis Imperfecta: A Systematic Review. J. Stomatol. Oral. Maxillofac. Surg. 2020, 121, 556–562. [Google Scholar] [CrossRef] [PubMed]
  44. Kim, H.-S.; Ahn, K.-J.; Kim, Y.-K. Clinical Diagnosis and Treatment of Herpes Zoster in an Immunocompromised Dental Patient: A Case Report. J. Korean Dent. Sci. 2014, 7, 99–105. [Google Scholar] [CrossRef]
  45. Kholin, A.V. Complications of radiotherapy and chemoradiotherapy of lymphogranulomatosis. Med. Radiol. 1984, 29, 66–74. [Google Scholar]
  46. Gupta, S.; Sreenivasan, V.; Patil, P.B. Dental Complications of Herpes Zoster: Two Case Reports and Review of Literature. Indian. J. Dent. Res. 2015, 26, 214–219. [Google Scholar] [CrossRef] [PubMed]
  47. Levin, M.J.; Oxman, M.N.; Zhang, J.H.; Johnson, G.R.; Stanley, H.; Hayward, A.R.; Caulfield, M.J.; Irwin, M.R.; Smith, J.G.; Clair, J.; et al. Varicella-Zoster Virus–Specific Immune Responses in Elderly Recipients of a Herpes Zoster Vaccine. J. Infect. Dis. 2008, 197, 825–835. [Google Scholar] [CrossRef] [PubMed]
  48. Smith, S.; Ross, J.W.; Scully, C. An Unusual Oral Complication of Herpes Zoster Infection. Oral. Surg. Oral. Med. Oral. Pathol. 1984, 57, 388–389. [Google Scholar] [CrossRef]
  49. Chatterjee, A.; Chattopadhyay, A.; Mandal, S.; De, N.; Hossain, M.A.; Pakhira, S. Delayed Presentation of Mandibular Osteonecrosis Following Herpes Zoster Infection—A Case Report. Ann. Maxillofac. Surg. 2023, 13, 220–223. [Google Scholar] [CrossRef]
  50. Brown, T.T.; Qaqish, R.B. Antiretroviral Therapy and the Prevalence of Osteopenia and Osteoporosis: A Meta-Analytic Review. In Database of Abstracts of Reviews of Effects (DARE): Quality-assessed Reviews [Internet]; Centre for Reviews and Dissemination: York, UK, 2006. [Google Scholar]
  51. Ihira, M.; Yoshikawa, T.; Ohashi, M.; Enomono, Y.; Akimoto, S.; Suga, S.; Saji, H.; Nishiyama, Y.; Asano, Y. Variation of Human Herpesvirus 7 Shedding in Saliva. J. Infect. Dis. 2003, 188, 1352–1354. [Google Scholar] [CrossRef]
  52. De Biscop, J.; Wackens, G. Alveolar bone necrosis as a complication of herpes zoster infection. Acta Stomatol. Belg. 1985, 82, 183–188. [Google Scholar] [PubMed]
  53. Rodrigues, J.B.; Poiares Baptista, A.; Leitao, A.; Lopes, T. Alveolar necrosis of the maxillary bone following trigeminal zona. Ann. Dermatol. Venereol. 1982, 109, 1057–1059. [Google Scholar] [PubMed]
  54. Pushpanshu, K.; Kaushik, R.; Srivastava, S.; Punyani, S.R. An Unusual Complication of Tooth Exfoliation and Osteonecrosis Following Herpes Zoster Infection of Trigeminal Nerve: A Case Report and Literature Review. Minerva Stomatol. 2013, 62, 241–245. [Google Scholar] [PubMed]
  55. Han, C.S.; Miller, W.; Haake, R.; Weisdorf, D. Varicella Zoster Infection after Bone Marrow Transplantation: Incidence, Risk Factors and Complications. Bone Marrow Transpl. 1994, 13, 277–283. [Google Scholar]
  56. Mueller, N.; Gilden, D.; Cohrs, R.; Mahalingam, R.; Nagel, M. Varicella Zoster Virus Infection: Clinical Features, Molecular Pathogenesis of Disease, and Latency. Neurol. Clin. 2008, 26, 675–697. [Google Scholar] [CrossRef] [PubMed]
  57. Peñarrocha-Diago, M.; Uribe-Origone, R. Etiology of Maxillary Necrosis. J. Oral. Maxillofac. Surg. 2003, 61, 1505. [Google Scholar] [CrossRef] [PubMed]
  58. Jonsson, L.; Tien, R.; Engström, M.; Thuomas, K.-Å. Gd-DPTA Enhanced MRI in Bell’s Palsy and Herpes Zoster Oticus: An Overview and Implications for Future Studies. Acta Oto-Laryngol. 1995, 115, 577–584. [Google Scholar] [CrossRef] [PubMed]
  59. Nortjé, C.J. General Practitioner’s Radiology Case 60. Herpes Zoster Infection. SADJ 2008, 63, 048. [Google Scholar]
  60. Gilden, D.; Nagel, M.; Cohrs, R. Varicella-Zoster. Handb. Clin. Neurol. 2014, 123, 265–283. [Google Scholar] [CrossRef]
  61. Melanson, M.; Chalk, C.; Georgevich, L.; Fett, K.; Lapierre, Y.; Duong, H.; Richardson, J.; Marineau, C.; Rouleau, G.A. Varicella-Zoster Virus DNA in CSF and Arteries in Delayed Contralateral Hemiplegia: Evidence for Viral Invasion of Cerebral Arteries. Neurology 1996, 47, 569–570. [Google Scholar] [CrossRef]
  62. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 Statement: An Updated Guideline for Reporting Systematic Reviews. PLoS Med. 2021, 18, e1003583. [Google Scholar] [CrossRef] [PubMed]
  63. Snow, J.L.; el-Azhary, R.A.; Gibson, L.E.; Estes, S.A.; Espy, M.J.; Smith, T.F. Granulomatous Vasculitis Associated With Herpes Virus: A Persistent, Painful, Postherpetic Papular Eruption. Mayo Clin. Proc. 1997, 72, 851–853. [Google Scholar] [CrossRef] [PubMed]
  64. Begazo, L.; Morante, A.; Espinoza Montes, C. Herpes simplex factors: Literature review. Rev. Cient. Odontol. 2022, 10, e099. [Google Scholar] [CrossRef] [PubMed]
  65. Alpantaki, K.; Katonis, P.; Hadjipavlou, A.G.; Spandidos, D.A.; Sourvinos, G. Herpes Virus Infection Can Cause Intervertebral Disc Degeneration: A Causal Relationship? J. Bone Jt. Surg. Br. 2011, 93, 1253–1258. [Google Scholar] [CrossRef] [PubMed]
  66. Yawn, B.P.; Gilden, D. The Global Epidemiology of Herpes Zoster. Neurology 2013, 81, 928–930. [Google Scholar] [CrossRef] [PubMed]
  67. Donahue, J.G.; Choo, P.W.; Manson, J.E.; Platt, R. The Incidence of Herpes Zoster. Arch. Intern. Med. 1995, 155, 1605–1609. [Google Scholar] [CrossRef] [PubMed]
  68. Crimi, S.; Fiorillo, L.; Bianchi, A.; D’Amico, C.; Amoroso, G.; Gorassini, F.; Mastroieni, R.; Marino, S.; Scoglio, C.; Catalano, F.; et al. Herpes Virus, Oral Clinical Signs and QoL: Systematic Review of Recent Data. Viruses 2019, 11, 463. [Google Scholar] [CrossRef] [PubMed]
  69. Siwamogstham, P.; Kuansuwan, C.; Reichart, P.A. Herpes Zoster in HIV Infection with Osteonecrosis of the Jaw and Tooth Exfoliation. Oral. Dis. 2006, 12, 500–505. [Google Scholar] [CrossRef]
  70. Epstein, J.B.; Marcoe, J.H. Topical Application of Capsaicin for Treatment of Oral Neuropathic Pain and Trigeminal Neuralgia. Oral. Surg. Oral. Med. Oral. Pathol. 1994, 77, 135–140. [Google Scholar] [CrossRef]
  71. Spruance, S.L.; Stewart, J.C.; Rowe, N.H.; McKeough, M.B.; Wenerstrom, G.; Freeman, D.J. Treatment of Recurrent Herpes Simplex Labialis with Oral Acyclovir. J. Infect. Dis. 1990, 161, 185–190. [Google Scholar] [CrossRef]
  72. Beutner, K.R.; Friedman, D.J.; Forszpaniak, C.; Andersen, P.L.; Wood, M.J. Valaciclovir Compared with Acyclovir for Improved Therapy for Herpes Zoster in Immunocompetent Adults. Antimicrob. Agents Chemother. 1995, 39, 1546–1553. [Google Scholar] [CrossRef] [PubMed]
  73. Wendling, D.; Streit, G.; Toussirot, E.; Prati, C. Herpes Zoster in Patients Taking TNFalpha Antagonists for Chronic Inflammatory Joint Disease. Jt. Bone Spine 2008, 75, 540–543. [Google Scholar] [CrossRef]
  74. Gholami, M.; Shahakbari, R.; Abdolahpour, S.; Hatami, M.; Roshanmir, A. Herpes Zoster Induced Alveolar Bone Necrosis in Immunocompromised Patients; Two Case Reports. Iran. J. Otorhinolaryngol. 2016, 28, 369–373. [Google Scholar]
  75. Tabrizi, R.; Dehghani Nazhvani, A.; Vahedi, A.; Gholami, M.; Zare, R.; Etemadi Parsa, R. Herpes Zoster Induced Osteomyelitis in the Immunocompromised Patients: A 10-Year Multicenter Study. J. Dent. 2014, 15, 112–116. [Google Scholar]
  76. Owotade, F.J.; Ugboko, V.I.; Kolude, B. Herpes Zoster Infection of the Maxilla: Case Report. J. Oral. Maxillofac. Surg. 1999, 57, 1249–1251. [Google Scholar] [CrossRef]
  77. Barrett, A.P. Herpes Zoster Virus Infection: A Clinicopathologic Review and Case Reports. Aust. Dent. J. 1990, 35, 328–332. [Google Scholar] [CrossRef]
  78. Warrier, S.A.; Ganesh, S.; Harikrishnan, T.; Balaji, B.; Venugopal, D.C.; Sushmitha, S. Herpes Zoster: A Case Report of a Rare Ramification Leading to Secondary Infection. Cureus 2023, 15, e36732. [Google Scholar] [CrossRef]
  79. Siakallis, G.; Spandidos, D.A.; Sourvinos, G. Herpesviridae and Novel Inhibitors. Antivir. Ther. 2009, 14, 1051–1064. [Google Scholar] [CrossRef] [PubMed]
  80. Chindia, M.L. HIV-Associated Fulminating Herpes Zoster Infection with Alveolar Necrosis and Tooth Exfoliation: A Case Report. Dent. Update 1997, 24, 126–128. [Google Scholar]
  81. Chaitanya, E.V.; Shruthi, T.V.; Shah, N.A. Late onset DCR surgical site herpes zoster in an immunocompetent patient: A rare presentation. Indian J. Ophthalmol. 2020, 68, 202–203. [Google Scholar] [CrossRef]
  82. Tsau, P.W.; Liao, M.F.; Hsu, J.L.; Hsu, H.-C.; Peng, C.H.; Lin, Y.C.; Kuo, H.C.; Ro, L.S. Clinical Presentations and Outcome Studies of Cranial Nerve Involvement in Herpes Zoster Infection: A Retrospective Single-Center Analysis. J. Clin. Med. 2020, 9, 946. [Google Scholar] [CrossRef] [PubMed]
  83. Song, J.M.; Seo, J.S.; Lee, J.Y. Mandibular osteonecrosis following herpes zoster infection in the mandibular branch of the trigeminal nerve: A case report and literature review. J. Korean Assoc. Oral Maxillofac. Surg. 2015, 41, 357. [Google Scholar] [CrossRef] [PubMed]
  84. Zhou, Y.; Zhao, N.; Huang, H.; Li, Q.; Guo, C.; Guo, Y. Left mandibular osteonecrosis following herpes zoster of the third branch of left trigeminal nerve: A case report. Beijing Da Xue Xue Bao Yi Xue Ban 2024, 56, 366–370. [Google Scholar] [CrossRef]
  85. Gan, E.Y.; Tian, E.A.L.; Tey, H.L. Management of Herpes Zoster and Post-Herpetic Neuralgia. Am. J. Clin. Dermatol. 2013, 14, 77–85. [Google Scholar] [CrossRef] [PubMed]
  86. Arikawa, J.; Mizushima, J.; Higaki, Y.; Hoshino, J.; Kawashima, M. Mandibular Alveolar Bone Necrosis after Trigeminal Herpes Zoster. Int. J. Dermatol. 2004, 43, 136–137. [Google Scholar] [CrossRef] [PubMed]
  87. Meer, S.; Coleman, H.; Altini, M.; Alexander, T. Mandibular Osteomyelitis and Tooth Exfoliation Following Zoster-CMV Co-Infection. Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. Endod. 2006, 101, 70–75. [Google Scholar] [CrossRef]
  88. Zirk, M.; Wenzel, C.; Buller, J.; Zöller, J.E.; Zinser, M.; Peters, F. Microbial Diversity in Infections of Patients with Medication-Related Osteonecrosis of the Jaw. Clin. Oral Investig. 2019, 23, 2143–2151. [Google Scholar] [CrossRef] [PubMed]
  89. Garg, K.; Mehrotra, A.; Singh, G.; Katyayan, R. Alveolar Osteonecrosis and Tooth Exfoliation in Herpes Zoster: A Rare Pediatric Case Report and Review of Literature. Int. J. Clin. Pediatr. Dent. 2020, 13, S106–S109. [Google Scholar] [CrossRef]
  90. Goswami, P.; Sharma, K.; Maiti, N.; Yadav, S.; Verma, V.; Puthenkandathil, R. Ozone: An Adjunct in Dental Treatment. J. Pharm. Bioallied Sci. 2024, 16, S2–S4. [Google Scholar] [CrossRef]
  91. Steiner, I. Herpes Virus Infection of the Peripheral Nervous System. Handb. Clin. Neurol. 2013, 115, 543–558. [Google Scholar] [CrossRef]
  92. Gatewood, J.B. Reconstruction of the Alveolar Ridge with Silicone-Dacron Implants: A Pilot Study. J. Oral. Surg. 1968, 26, 441–448. [Google Scholar] [PubMed]
  93. Eisenberg, E. Intraoral Isolated Herpes Zoster. Oral. Surg. Oral. Med. Oral. Pathol. 1978, 45, 214–219. [Google Scholar] [CrossRef] [PubMed]
  94. Sasada, K.; Yasue, T.; Akutsu, J.; Shinjô, H. Clinical study and treatment of herpes zoster (author’s transl). Nihon Hifuka Gakkai Zasshi 1976, 86, 615–622. [Google Scholar] [PubMed]
  95. Amagasa, T.; Shiojima, K.; Sato, K.; Mase, M.; Wake, H.; Fujii, E.; Shioda, S. Herpes Zoster Localized to the Oral Mucosa: Report of Two Cases. Jpn. J. Oral Maxillofac. Surg. 1980, 26, 419–425. [Google Scholar] [CrossRef]
  96. Rook, A.; Wilkinson, D.S.; Ebling, F.J.G. Textbook of Dermatology, 3rd. ed.; Blackwell Scientific: Oxford, UK, 1979; 1149p, Available online: https://pesquisa.bvsalud.org/portal/resource/pt/biblio-1230927 (accessed on 26 June 2024).
  97. Hasegawa, T. Further Electron Microscopic Observations of Herpes Zoster Virus. Arch. Dermatol. 1971, 103, 45–49. [Google Scholar] [CrossRef]
  98. Dechaume, N.; Descrozailles, C.; Garlopeau, F.; Robert, J. Localized mandibular necrosis during trigeminal herpes. Rev. Stomatol. 1955, 56, 516–521. [Google Scholar]
  99. Saxena, K.N.; Srivastava, M.C.; Tandon, M.K. Herpes Zoster with An Unusual Sequela. J. Indian. Med. Assoc. 1963, 41, 456–458. [Google Scholar]
  100. Goldoni, R.; Dolci, C.; Boccalari, E.; Inchingolo, F.; Paghi, A.; Strambini, L.; Galimberti, D.; Tartaglia, G.M. Salivary Biomarkers of Neurodegenerative and Demyelinating Diseases and Biosensors for Their Detection. Ageing Res. Rev. 2022, 76, 101587. [Google Scholar] [CrossRef] [PubMed]
  101. Inchingolo, A.D.; Ceci, S.; Patano, A.; Inchingolo, A.M.; Montenegro, V.; Di Pede, C.; Malcangi, G.; Marinelli, G.; Coloccia, G.; Garibaldi, M.; et al. Elastodontic Therapy of Hyperdivergent Class II Patients Using AMCOP® Devices: A Retrospective Study. Appl. Sci. 2022, 12, 3259. [Google Scholar] [CrossRef]
  102. Malcangi, G.; Inchingolo, A.D.; Patano, A.; Coloccia, G.; Ceci, S.; Garibaldi, M.; Inchingolo, A.M.; Piras, F.; Cardarelli, F.; Settanni, V.; et al. Impacted Central Incisors in the Upper Jaw in an Adolescent Patient: Orthodontic-Surgical Treatment—A Case Report. Appl. Sci. 2022, 12, 2657. [Google Scholar] [CrossRef]
  103. Ballini, A.; Cantore, S.; Signorini, L.; Saini, R.; Scacco, S.; Gnoni, A.; Inchingolo, A.D.; De Vito, D.; Santacroce, L.; Inchingolo, F.; et al. Efficacy of Sea Salt-Based Mouthwash and Xylitol in Improving Oral Hygiene among Adolescent Population: A Pilot Study. Int. J. Environ. Res. Public Health 2021, 18, 44. [Google Scholar] [CrossRef] [PubMed]
  104. Rapone, B.; Inchingolo, A.D.; Trasarti, S.; Ferrara, E.; Qorri, E.; Mancini, A.; Montemurro, N.; Scarano, A.; Inchingolo, A.M.; Dipalma, G.; et al. Long-Term Outcomes of Implants Placed in Maxillary Sinus Floor Augmentation with Porous Fluorohydroxyapatite (Algipore® FRIOS®) in Comparison with Anorganic Bovine Bone (Bio-Oss®) and Platelet Rich Plasma (PRP): A Retrospective Study. J. Clin. Med. 2022, 11, 2491. [Google Scholar] [CrossRef] [PubMed]
  105. Rudd, T.; Chai, B.Y.; Gurunluoglu, R.; Glasgow, M. Mandibular Osteonecrosis and Ramsay Hunt Syndrome Following a Case of Herpes Zoster. J. Oral. Maxillofac. Surg. 2014, 72, 1974.e1–1974.e6. [Google Scholar] [CrossRef] [PubMed]
  106. Cloarec, N.; Zaegel-Faucher, O.; Bregigeon, S.; Cano, C.E.; Chossegros, C.; Wajszczak, B.; Poizot-Martin, I. Mandibular osteonecrosis and dental exfoliation after trigeminal zoster in an HIV-infected patient: Case report and review of the literature. Aids 2014, 28, 448–450. [Google Scholar] [CrossRef]
  107. Vickery, I.M.; Midda, M. Dental Complications of Cytotoxic Therapy in Hodgkin’s Disease—A Case Report. Br. J. Oral. Surg. 1976, 13, 282–288. [Google Scholar] [CrossRef] [PubMed]
  108. Nisi, M.; Ferla, F.; Graziani, F.; Gabriele, M. Osteonecrosis of the Jaws Related to Corticosteroids Therapy: A Case Report. Ann. Di Stomatol. 2014, 5, 29–30. [Google Scholar]
  109. Rowbotham, M.C.; Davies, P.S.; Verkempinck, C.; Galer, B.S. Lidocaine patch: Double-blind controlled study of a new treatment method for post-herpetic neuralgia. Pain 1996, 65, 39–44. [Google Scholar] [CrossRef] [PubMed]
  110. Mendieta, C.; Miranda, J.; Brunet, L.I.; Gargallo, J.; Berini, L. Alveolar Bone Necrosis and Tooth Exfoliation Following Herpes Zoster Infection: A Review of the Literature and Case Report. J. Periodontol. 2005, 76, 148–153. [Google Scholar] [CrossRef] [PubMed]
  111. Francis, M.; Subramanian, K.; Sankari, S.L.; Potluri, V.L.A.; Prabakaran, A. Herpes Zoster with Post Herpetic Neuralgia Involving the Right Maxillary Branch of Trigeminal Nerve: A Case Report and Review of Literature. J. Clin. Diagn. Res. 2017, 11, ZD40. [Google Scholar] [CrossRef]
  112. Bennardo, F.; Bennardo, L.; Duca, E.; Patruno, C.; Fortunato, L.; Amerigo, G.; Nisticò, S. Autologous Platelet-Rich Fibrin Injections in the Management of Facial Cutaneous Sinus Tracts Secondary to Medication-Related Osteonecrosis of the Jaw. Dermatol. Ther. 2020, 33, e13334. [Google Scholar] [CrossRef]
  113. Bennardo, F.; Buffone, C.; Giudice, A. New Therapeutic Opportunities for COVID-19 Patients with Tocilizumab: Possible Correlation of Interleukin-6 Receptor Inhibitors with Osteonecrosis of the Jaws. Oral. Oncol. 2020, 106, 104659. [Google Scholar] [CrossRef] [PubMed]
  114. Martin, D.F.; Sierra-Madero, J.; Walmsley, S.; Wolitz, R.A.; Macey, K.; Georgiou, P.; Robinson, C.A.; Stempien, M.J. Valganciclovir Study Group A Controlled Trial of Valganciclovir as Induction Therapy for Cytomegalovirus Retinitis. N. Engl. J. Med. 2002, 346, 1119–1126. [Google Scholar] [CrossRef] [PubMed]
  115. Lalezari, J.; Schacker, T.; Feinberg, J.; Gathe, J.; Lee, S.; Cheung, T.; Kramer, F.; Kessler, H.; Corey, L.; Drew, W.L.; et al. A Randomized, Double-Blind, Placebo-Controlled Trial of Cidofovir Gel for the Treatment of Acyclovir-Unresponsive Mucocutaneous Herpes Simplex Virus Infection in Patients with AIDS. J. Infect. Dis. 1997, 176, 892–898. [Google Scholar] [CrossRef] [PubMed]
  116. Oxman, M.N. Herpes Zoster Pathogenesis and Cell-Mediated Immunity and Immunosenescence. J. Am. Osteopath. Assoc. 2009, 109, S13–S17. [Google Scholar] [PubMed]
  117. Oxman, M.N.; Levin, M.J.; Johnson, G.R.; Schmader, K.E.; Straus, S.E.; Gelb, L.D.; Arbeit, R.D.; Simberkoff, M.S.; Gershon, A.A.; Davis, L.E.; et al. A Vaccine to Prevent Herpes Zoster and Postherpetic Neuralgia in Older Adults. N. Engl. J. Med. 2005, 352, 2271–2284+2365. [Google Scholar] [CrossRef] [PubMed]
  118. Portenoy, R.K.; Duma, C.; Foley, K.M. Acute Herpetic and Postherpetic Neuralgia: Clinical Review and Current Management. Ann. Neurol. 1986, 20, 651–664. [Google Scholar] [CrossRef] [PubMed]
  119. Meyers, J.D.; Wade, J.C.; Shepp, D.H.; Newton, B. Acyclovir Treatment of Varicella-Zoster Virus Infection in the Compromised Host. Transplantation 1984, 37, 571–574. [Google Scholar] [CrossRef] [PubMed]
  120. Haefeli, W.E.; Schoenenberger, R.A.; Weiss, P.; Ritz, R.F. Acyclovir-Induced Neurotoxicity: Concentration-Side Effect Relationship in Acyclovir Overdose. Am. J. Med. 1993, 94, 212–215. [Google Scholar] [CrossRef] [PubMed]
  121. Masur, H.; Whitcup, S.M.; Cartwright, C.; Polis, M.; Nussenblatt, R. Advances in the Management of AIDS-Related Cytomegalovirus Retinitis. Ann. Intern. Med. 1996, 125, 126–136. [Google Scholar] [CrossRef]
  122. Bean, B.; Aeppli, D. Adverse Effects of High-Dose Intravenous Acyclovir in Ambulatory Patients with Acute Herpes Zoster. J. Infect. Dis. 1985, 151, 362–365. [Google Scholar] [CrossRef]
  123. Rolston, K.V.; Manzullo, E.; Elting, L.; Frisbee-Hume, S.; Rodriguez, S.; Rubenstein, E.B. Ambulatory Management of Varicella-Zoster Virus Infection in Immunocompromised Cancer Patients. Support. Care Cancer 1998, 6, 57–62. [Google Scholar] [CrossRef] [PubMed]
  124. Kamarthi, N.; Narasimha, G.; Lingappa, A. An Unusual Case of Osteonecrosis and Spontaneous Tooth Exfoliation Following Trigeminal Herpes Zoster in a HIV Seropositive Patient. Int. J. Oral Med. Sci. 2009, 8, 52–59. [Google Scholar] [CrossRef]
  125. Henle, G.; Henle, W.; Clifford, P.; Diehl, V.; Kafuko, G.W.; Kirya, B.G.; Klein, G.; Morrow, R.H.; Munube, G.M.; Pike, P.; et al. Antibodies to Epstein-Barr Virus in Burkitt’s Lymphoma and Control Groups. J. Natl. Cancer Inst. 1969, 43, 1147–1157. [Google Scholar] [PubMed]
  126. De Clercq, E. Antiviral Drugs in Current Clinical Use. J. Clin. Virol. 2004, 30, 115–133. [Google Scholar] [CrossRef] [PubMed]
  127. Kaur, R.; Rani, P.; Malhotra, D.; Kaur, R.; Dass, P. A Rare Case Report and Appraisal of the Literature on Spontaneous Tooth Exfoliation Associated with Trigeminal Herpes Zoster. Oral. Maxillofac. Surg. 2016, 20, 331–336. [Google Scholar] [CrossRef] [PubMed]
  128. Keskinruzgar, A.; Demirkol, M.; Ege, B.; Aras, M.H.; Ay, S. Rare Involvement of Herpes Zoster in the Mandibular Branch of the Trigeminal Nerve: A Case Report and Review of the Literature. Quintessence Int. 2015, 46, 168. [Google Scholar] [CrossRef]
  129. Ragozzino, M.W.; Melton, L.J.; Kurland, L.T.; Chu, C.P.; Perry, H.O. Population-Based Study of Herpes Zoster and Its Sequelae. Medicine 1982, 61, 310–316. [Google Scholar] [CrossRef] [PubMed]
  130. Bowsher, D. Post-Herpetic Neuralgia in Older Patients. Drugs Aging 1994, 5, 411–418. [Google Scholar] [CrossRef] [PubMed]
  131. Hope-Simpson, R.E. Postherpetic Neuralgia. J. R. Coll. Gen. Pract. 1975, 25, 571–575. [Google Scholar]
  132. Hope-Simpson, R.E. The Nature Of Herpes Zoster: A Long-Term Study And A New Hypothesis. Proc. R. Soc. Med. 1965, 58, 9–20. [Google Scholar]
  133. Kost, R.; Straus, S. Postherpetic Neuralgia—Pathogenesis, Treatment, and Prevention. N. Engl. J. Med. 1996, 335, 32–42. [Google Scholar] [CrossRef] [PubMed]
  134. Meijer, E.; Boland, G.J.; Verdonck, L.F. Prevention of Cytomegalovirus Disease in Recipients of Allogeneic Stem Cell Transplants. Clin. Microbiol. Rev. 2003, 16, 647–657. [Google Scholar] [CrossRef] [PubMed]
  135. Goon, W.W.Y.; Jacobsen, P.L. Prodromal Odontalgia and Multiple Devitalized Teeth Caused by a Herpes Zoster Infection of the Trigeminal Nerve: Report of Case. J. Am. Dent. Assoc. 1988, 116, 500–504. [Google Scholar] [CrossRef] [PubMed]
  136. Inchingolo, F.; Inchingolo, A.M.; Latini, G.; Palmieri, G.; Di Pede, C.; Trilli, I.; Ferrante, L.; Inchingolo, A.D.; Palermo, A.; Lorusso, F.; et al. Application of Graphene Oxide in Oral Surgery: A Systematic Review. Materials 2023, 16, 6293. [Google Scholar] [CrossRef] [PubMed]
  137. Mendel, D.B.; Barkhimer, D.B.; Chen, M.S. Biochemical Basis for Increased Susceptibility to Cidofovir of Herpes Simplex Viruses with Altered or Deficient Thymidine Kinase Activity. Antimicrob. Agents Chemother. 1995, 39, 2120–2122. [Google Scholar] [CrossRef] [PubMed]
  138. Okamura, T.; Hatsukawa, Y.; Arai, H.; Inoue, M.; Kawa, K. Blood Stem-Cell Transplantation for Chronic Active Epstein-Barr Virus with Lymphoproliferation. Lancet 2000, 356, 223–224. [Google Scholar] [CrossRef] [PubMed]
  139. Sato, K.; Adachi, K.; Nakamura, H.; Asano, K.; Watanabe, A.; Adachi, R.; Kiuchi, M.; Kobayashi, K.; Matsuki, T.; Kaise, T.; et al. Burden of Herpes Zoster and Postherpetic Neuralgia in Japanese Adults 60 Years of Age or Older: Results from an Observational, Prospective, Physician Practice-based Cohort Study. J. Dermatol. 2016, 44, 414–422. [Google Scholar] [CrossRef] [PubMed]
  140. Irwin, M.; Costlow, C.; Williams, H.; Artin, K.; Chan, C.; Stinson, D.; Levin, M.; Hayward, A.; Oxman, M. Cellular Immunity to Varicella-Zoster Virus in Patients with Major Depression. J. Infect. Dis. 1998, 178 (Suppl. S1), S104–S108. [Google Scholar] [CrossRef]
  141. Martinez, C.M.; Luks-Golger, D.B. Cidofovir Use in Acyclovir-Resistant Herpes Infection. Ann. Pharmacother. 1997, 31, 1519–1521. [Google Scholar]
  142. Grassi, F.R.; Ciccolella, F.; D’Apolito, G.; Papa, F.; Iuso, A.; Salzo, A.E.; Trentadue, R.; Nardi, G.M.; Scivetti, M.; De Matteo, M.; et al. Effect of Low-Level Laser Irradiation on Osteoblast Proliferation and Bone Formation. J. Biol. Regul. Homeost. Agents 2011, 25, 603–614. [Google Scholar]
  143. Bavetta, G.; Bavetta, G.; Randazzo, V.; Cavataio, A.; Paderni, C.; Grassia, V.; Dipalma, G.; Isacco, C.G.; Scarano, A.; Vito, D.D.; et al. A Retrospective Study on Insertion Torque and Implant Stability Quotient (Isq) as Stability Parameters for Immediate Loading of Implants in Fresh Extraction Sockets. BioMed Res. Int. 2019, 2019, 9720419. [Google Scholar] [CrossRef] [PubMed]
  144. Inchingolo, A.D.; Malcangi, G.; Semjonova, A.; Inchingolo, A.M.; Patano, A.; Coloccia, G.; Ceci, S.; Marinelli, G.; Di Pede, C.; Ciocia, A.M.; et al. Oralbiotica/Oralbiotics: The Impact of Oral Microbiota on Dental Health and Demineralization: A Systematic Review of the Literature. Children 2022, 9, 1014. [Google Scholar] [CrossRef] [PubMed]
  145. Inchingolo, A.D.; Patano, A.; Coloccia, G.; Ceci, S.; Inchingolo, A.M.; Marinelli, G.; Malcangi, G.; Di Pede, C.; Garibaldi, M.; Ciocia, A.M.; et al. Treatment of Class III Malocclusion and Anterior Crossbite with Aligners: A Case Report. Med. 2022, 58, 603. [Google Scholar] [CrossRef] [PubMed]
  146. Inchingolo, F.; Tatullo, M.; Abenavoli, F.M.; Marrelli, M.; Inchingolo, A.D.; Villabruna, B.; Inchingolo, A.M.; Dipalma, G. Severe Anisocoria after Oral Surgery under General Anesthesia. Int. J. Med. Sci. 2010, 7, 314–318. [Google Scholar] [CrossRef]
  147. de Wit, R.; Schattenkerk, J.K.; Boucher, C.A.; Bakker, P.J.; Veenhof, K.H.; Danner, S.A. Clinical and Virological Effects of High-Dose Recombinant Interferon-Alpha in Disseminated AIDS-Related Kaposi’s Sarcoma. Lancet 1988, 2, 1214–1217. [Google Scholar] [CrossRef]
  148. Hudson, C.D.; Vickers, R.A. Clinicopathologic Observations in Prodromal Herpes Zoster of the Fifth Cranial Nerve: Report of a Case. Oral. Surg. Oral. Med. Oral. Pathol. 1971, 31, 494–501. [Google Scholar] [CrossRef] [PubMed]
  149. Alshehri, M.; Esht, V.; Ghosh, A.; Sharma, R.; Shaphe, M. Concurrent Involvement of Trigeminal and Facial Nerves in Herpes Zoster. Anatol. J. Fam. Med. 2023, 6, 123–126. [Google Scholar] [CrossRef]
  150. Gargiulo Isacco, C.; Inchingolo, A.D.; Nguyen Cao, K.D.; Malcangi, G.; Paduanelli, G.; Pham Hung, V.; Tran Cong, T.; Bordea, I.R.; Scarano, A.; Laforgia, A.; et al. The Bad Relationship, Osteo-Decay and Diabetes Type 2 Searching for a Link: A Literature Review. J. Biol. Regul. Homeost. Agents 2021, 35, 253–269. [Google Scholar] [CrossRef]
  151. Inchingolo, A.M.; Patano, A.; Piras, F.; Mancini, A.; Inchingolo, A.D.; Paduanelli, G.; Inchingolo, F.; Palermo, A.; Dipalma, G.; Malcangi, G. Interconnection between Microbiota-Gut-Brain Axis and Autism Spectrum Disorder Comparing Therapeutic Options: A Scoping Review. Microorganisms 2023, 11, 1477. [Google Scholar] [CrossRef]
  152. Dipalma, G.; Inchingolo, A.D.; Inchingolo, A.M.; Piras, F.; Carpentiere, V.; Garofoli, G.; Azzollini, D.; Campanelli, M.; Paduanelli, G.; Palermo, A.; et al. Artificial Intelligence and Its Clinical Applications in Orthodontics: A Systematic Review. Diagnostics 2023, 13, 3677. [Google Scholar] [CrossRef]
  153. Inchingolo, F.; Dipalma, G.; Paduanelli, G.; De Oliveira, L.A.; Inchingolo, A.M.; Georgakopoulos, P.I.; Inchingolo, A.D.; Malcangi, G.; Athanasiou, E.; Fotopoulou, E.; et al. Computer-Based Quantification of an Atraumatic Sinus Augmentation Technique Using CBCT. J. Biol. Regul. Homeost. Agents 2019, 33, 31–39. [Google Scholar] [PubMed]
  154. Cotton, S.; Belcher, J.; Rose, P.; Jagadeesan, S.; Neal, R.; Cotton, S.J.; Belcher, J.; Rose, P.K.; Jagadeesan, S. Neal RDThe Risk of a Subsequent Cancer Diagnosis after Herpes Zoster Infection: Primary Care Database Study. Br. J. Cancer 2013, 108, 721–726. [Google Scholar] [CrossRef] [PubMed]
  155. Patel, R.; Snydman, D.R.; Rubin, R.H.; Ho, M.; Pescovitz, M.; Martin, M.; Paya, C.V. Cytomegalovirus Prophylaxis in Solid Organ Transplant Recipients. Transplantation 1996, 61, 1279–1289. [Google Scholar] [CrossRef] [PubMed]
  156. Kishore-kumar, R.; Max, M.; Schafer, S.; Gaughan, A.; Smoller, B.; Gracely, R.; Dubner, R. Desipramine Relieves Postherpetic Neuralgia. Clin. Pharmacol. Ther. 1990, 47, 305–312. [Google Scholar] [CrossRef]
  157. Khan, A.A.; Morrison, A.; Hanley, D.A.; Felsenberg, D.; McCauley, L.K.; O’Ryan, F.; Reid, I.R.; Ruggiero, S.L.; Taguchi, A.; Tetradis, S.; et al. Diagnosis and Management of Osteonecrosis of the Jaw: A Systematic Review and International Consensus. J. Bone Miner. Res. 2015, 30, 3–23. [Google Scholar] [CrossRef] [PubMed]
  158. Inchingolo, A.M.; Malcangi, G.; Piras, F.; Palmieri, G.; Settanni, V.; Riccaldo, L.; Morolla, R.; Buongiorno, S.; Ruvo, E.; Inchingolo, A.D.; et al. Precision Medicine on the Effects of Microbiota on Head–Neck Diseases and Biomarkers Diagnosis. J. Pers. Med. 2023, 13, 933. [Google Scholar] [CrossRef] [PubMed]
  159. Inchingolo, A.D.; Inchingolo, A.M.; Piras, F.; Malcangi, G.; Patano, A.; Di Pede, C.; Netti, A.; Ciocia, A.M.; Corriero, A.; Semjonova, A.; et al. A Systematic Review of Positional Plagiocephaly Prevention Methods for Patients in Development. Appl. Sci. 2022, 12, 11172. [Google Scholar] [CrossRef]
  160. Patano, A.; Cardarelli, F.; Montenegro, V.; Ceci, S.; Inchingolo, A.D.; Semjonova, A.; Palmieri, G.; Di Pede, C.; Mancini, A.; Maggiore, M.E.; et al. Early Functional Orthodontic Treatment of Bad Oral Habits with AMCOP® Bio-Activators. J. Biol. Regul. Homeost. Agents 2022, 36, 91–110. [Google Scholar]
  161. Malcangi, G.; Patano, A.; Palmieri, G.; Riccaldo, L.; Pezzolla, C.; Mancini, A.; Inchingolo, A.D.; Di Venere, D.; Piras, F.; Inchingolo, F.; et al. Oral Piercing: A Pretty Risk—A Scoping Review of Local and Systemic Complications of This Current Widespread Fashion. Int. J. Environ. Res. Public Health 2023, 20, 5744. [Google Scholar] [CrossRef]
  162. Christiansen, N.P.; Haake, R.J.; Hurd, D.D. Early Herpes Zoster Infection in Adult Patients with Hodgkin’s Disease Undergoing Autologous Bone Marrow Transplant. Bone Marrow Transpl. 1991, 7, 435–437. [Google Scholar]
  163. Cunningham, A.L.; Lal, H.; Martina, K.; Roman, C.; Shinn-Jang, H.; Javier, D.-D.; Olivier, G.; Myron, J.L.; McElhaney Janet, E.; Joan, P.B.; et al. Efficacy of the Herpes Zoster Subunit Vaccine in Adults 70 Years of Age or Older. N. Engl. J. Med. 2016, 375, 1019–1032. [Google Scholar] [CrossRef] [PubMed]
  164. Mckenna, K.F.; Warneke, L.B. Encephalitis Associated with Herpes Zoster: A Case Report and Review. Can. J. Psychiatry 1992, 37, 271–273. [Google Scholar] [CrossRef]
  165. Straus, S.E.; Reinhold, W.; Smith, H.A.; Ruyechan, W.T.; Henderson, D.K.; Blaese, R.M.; Hay, J. Endonuclease Analysis of Viral DNA from Varicella and Subsequent Zoster Infections in the Same Patient. N. Engl. J. Med. 1984, 311, 1362–1364. [Google Scholar] [CrossRef]
  166. Faure, E.; Engels-Deutsch, M.; Paraschiv, E.-A.; Gérard, E.; Curien, R. Mandibular Osteonecrosis Following Herpes Zoster Infection: Report of a Rare Case with a Literature Review. Clin. Case Rep. 2021, 9, e04196. [Google Scholar] [CrossRef] [PubMed]
  167. Thorley-Lawson, D.A.; Miyashita, E.M.; Khan, G. Epstein-Barr Virus and the B Cell: That’s All It Takes. Trends Microbiol. 1996, 4, 204–208. [Google Scholar] [CrossRef] [PubMed]
  168. Kuzushima, K.; Yamamoto, M.; Kimura, H.; Ando, Y.; Kudo, T.; Tsuge, I.; Morishima, T. Establishment of Anti-Epstein-Barr Virus (EBV) Cellular Immunity by Adoptive Transfer of Virus-Specific Cytotoxic T Lymphocytes from an HLA-Matched Sibling to a Patient with Severe Chronic Active EBV Infection. Clin. Exp. Immunol. 1996, 103, 192–198. [Google Scholar] [CrossRef]
  169. Werner, R.; Nikkels, A.; Marinović, B.; Schäfer, M.; Czarnecka-Operacz, M.; Agius, A.; Bata-Csörgő, Z.; Breuer, J.; Girolomoni, G.; Gross, G.; et al. European Consensus-Based (S2k) Guideline on the Management of Herpes Zoster—Guided by the European Dermatology Forum (EDF) in Cooperation with the European Academy of Dermatology and Venereology (EADV), Part 2: Treatment. J. Eur. Acad. Dermatol. Venereol. 2016, 31, 20–29. [Google Scholar] [CrossRef]
  170. Pescovitz, M.D. Formulary Considerations for Drugs Used to Prevent Cytomegalovirus Disease. Am. J. Health Syst. Pharm. 2003, 60, S17–S21. [Google Scholar] [CrossRef]
  171. Huang, K.; Wang, Y.; Huang, Y.; Han, S.; Yang, Y.; Qu, P.; Liang, B.; Zhen, Q.; Chen, W.; Lin, Y. Infection May Play an Important Role in the Pathogenesis of Alveolar Osteonecrosis Following Facial Herpes Zoster: A Case Report and Literature Review. BMC Oral. Health 2024, 24, 409. [Google Scholar] [CrossRef]
  172. Safrin, S.; Assaykeen, T.; Follansbee, S.; Mills, J. Foscarnet Therapy for Acyclovir-Resistant Mucocutaneous Herpes Simplex Virus Infection in 26 AIDS Patients: Preliminary Data. J. Infect. Dis. 1990, 161, 1078–1084. [Google Scholar] [CrossRef]
  173. Wagstaff, A.J.; Bryson, H.M. Foscarnet. A Reappraisal of Its Antiviral Activity, Pharmacokinetic Properties and Therapeutic Use in Immunocompromised Patients with Viral Infections. Drugs 1994, 48, 199–226. [Google Scholar] [CrossRef]
  174. Stanberry, L.R.; Spruance, S.L.; Cunningham, A.L.; Bernstein, D.I.; Mindel, A.; Sacks, S.; Tyring, S.; Aoki, F.Y.; Slaoui, M.; Denis, M.; et al. Glycoprotein-D-Adjuvant Vaccine to Prevent Genital Herpes. N. Engl. J. Med. 2002, 347, 1652–1661. [Google Scholar] [CrossRef] [PubMed]
  175. Watson, C.P.N. Herpes Zoster and Postherpetic Neuralgia. CMAJ 2010, 182, 1713–1714. [Google Scholar] [CrossRef]
  176. Liu, B.T.; Xue, K.; Fan, B.F.; Cui, Y. Interpretation of the expert consensus on the whole-process management of herpes zoster-associated pain. Zhonghua Yi Xue Za Zhi 2022, 102, 3156–3159. [Google Scholar] [CrossRef] [PubMed]
  177. Fortunato, L.; Bennardo, F.; Buffone, C.; Giudice, A. Is the Application of Platelet Concentrates Effective in the Prevention and Treatment of Medication-Related Osteonecrosis of the Jaw? A Systematic Review. J. Cranio-Maxillofac. Surg. 2020, 48, 268–285. [Google Scholar] [CrossRef] [PubMed]
  178. Fernandes, N.F.; Malliah, R.; Stitik, T.P.; Rozdeba, P.; Lambert, W.C.; Schwartz, R.A. Herpes Zoster Following Intra-Articular Corticosteroid Injection. Acta Dermatovenerol Alp Pannonica Adriat 2009, 18, 28–30. [Google Scholar] [PubMed]
  179. Gregory, W.B., Jr.; Brooks, L.E.; Penick, E.C. Herpes Zoster Associated with Pulpless Teeth. J. Endod. 1975, 1, 32–35. [Google Scholar] [CrossRef]
  180. Crouch, A.E.; Hohman, M.H.; Moody, M.P.; Andaloro, C. Ramsay Hunt Syndrome; StatPearls—NCBI Bookshelf: St. Petersburg, FL, USA, 2020. Available online: https://www.ncbi.nlm.nih.gov/books/NBK557409/ (accessed on 28 June 2024).
  181. Severson, J.L.; Tyring, S.K. Relation between Herpes Simplex Viruses and Human Immunodeficiency Virus Infections. Arch. Dermatol. 1999, 135, 1393–1397. [Google Scholar] [CrossRef]
  182. Mahajan, V.; Ranjan, N.; Sharma, S.; Sharma, N. Spontaneous Tooth Exfoliation after Trigeminal Herpes Zoster: A Case Series of an Uncommon Complication. Indian. J. Dermatol. 2013, 58, 244. [Google Scholar] [CrossRef]
  183. Nair, P.; Gharote, H.; Singh, P.; Jain-Choudhary, P. Herpes Zoster on the Face in the Elderly. Case Rep. 2014, 2014, bcr2013200101. [Google Scholar] [CrossRef]
  184. Ahmad, S.S.; Suan, A.; Alexander, S. Herpes Zoster Ophthalmicus, Central Retinal Artery Occlusion, and Neovascular Glaucoma in an Immunocompetent Individual. J. Ophthalmic Vis. Res. 2019, 14, 97. [Google Scholar] [CrossRef] [PubMed]
  185. Solomon, C.S.; Coffiner, M.O.; Chalfin, H.E. Herpes Zoster Revisited: Implicated in Root Resorption. J. Endod. 1986, 12, 210–213. [Google Scholar] [CrossRef] [PubMed]
  186. Grinde, B. Herpesviruses: Latency and Reactivation—Viral Strategies and Host Response. J. Oral. Microbiol. 2013, 5, 22766. [Google Scholar] [CrossRef] [PubMed]
  187. Inchingolo, F.; Tatullo, M.; Pacifici, A.; Gargari, M.; Inchingolo, A.D.; Inchingolo, A.M.; Dipalma, G.; Marrelli, M.; Abenavoli, F.M.; Pacifici, L. Use of Dermal-Fat Grafts in the Post-Oncological Reconstructive Surgery of Atrophies in the Zygomatic Region: Clinical Evaluations in the Patients Undergone to Previous Radiation Therapy. Head. Face Med. 2012, 8, 3. [Google Scholar] [CrossRef] [PubMed]
  188. Inchingolo, F.; Tatullo, M.; Marrelli, M.; Inchingolo, A.M.; Tarullo, A.; Inchingolo, A.D.; Dipalma, G.; Brunetti, S.P.; Tarullo, A.; Cagiano, R. Combined Occlusal and Pharmacological Therapy in the Treatment of Temporo-Mandibular Disorders. Eur. Rev. Med. Pharmacol. Sci. 2011, 15, 1296–1300. [Google Scholar]
  189. Inchingolo, F.; Tatullo, M.; Abenavoli, F.M.; Marrelli, M.; Inchingolo, A.D.; Corelli, R.; Inchingolo, A.M.; Dipalma, G. Surgical Treatment of Depressed Scar: A Simple Technique. Int. J. Med. Sci. 2011, 8, 377–379. [Google Scholar] [CrossRef] [PubMed]
  190. Dang, Q.T.; Huynh, T.D.; Inchingolo, F.; Dipalma, G.; Inchingolo, A.D.; Cantore, S.; Paduanelli, G.; Nguyen, K.C.D.; Ballini, A.; Isacco, C.G.; et al. Human Chondrocytes from Human Adipose Tissue-Derived Mesenchymal Stem Cells Seeded on a Dermal-Derived Collagen Matrix Sheet: Our Preliminary Results for a Ready to Go Biotechnological Cartilage Graft in Clinical Practice. Stem Cells Int. 2021, 2021, 6664697. [Google Scholar] [CrossRef] [PubMed]
  191. Choi, H.J.; Kim, J.H.; Lee, Y.M. Herpes zoster developing within recent subciliary incision scar. J. Craniofac. Surg. 2012, 23, 930–931. [Google Scholar] [CrossRef] [PubMed]
  192. Park, K.-S. Maxillary Osteonecrosis Related with Herpes Zoster: A Case Report and Review of the Literature. Medicina 2024, 60, 883. [Google Scholar] [CrossRef]
  193. Nicolatou-Galitis, O.; Schiødt, M.; Mendes, R.A.; Ripamonti, C.; Hope, S.; Drudge-Coates, L.; Niepel, D.; Van den Wyngaert, T. Medication-Related Osteonecrosis of the Jaw: Definition and Best Practice for Prevention, Diagnosis, and Treatment. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2019, 127, 117–135. [Google Scholar] [CrossRef]
  194. Takeda, S.; Karsenty, G. Molecular Bases of the Sympathetic Regulation of Bone Mass. Bone 2008, 42, 837–840. [Google Scholar] [CrossRef]
  195. Kurtzke, J.F. Neuroepidemiology. Ann. Neurol. 1984, 16, 265–277. [Google Scholar] [CrossRef] [PubMed]
  196. Dezube, B.J. New Therapies for the Treatment of AIDS-Related Kaposi Sarcoma. Curr. Opin. Oncol. 2000, 12, 445–449. [Google Scholar] [CrossRef]
  197. Federico, F.; Pedone, D.; Lamberti, P.; Achille, P.; Camicia, M.; Carella, A.; Ferrari, E. Ophthalmic Herpes Zoster with Contralateral Hemiparesis: A Case Report. J. Neurol. 1982, 228, 283–287. [Google Scholar] [CrossRef] [PubMed]
  198. Spector, S.A.; McKinley, G.F.; Lalezari, J.P.; Samo, T.; Andruczk, R.; Follansbee, S.; Sparti, P.D.; Havlir, D.V.; Simpson, G.; Buhles, W.; et al. Oral Ganciclovir for the Prevention of Cytomegalovirus Disease in Persons with AIDS. Roche Cooperative Oral Ganciclovir Study Group. N. Engl. J. Med. 1996, 334, 1491–1497. [Google Scholar] [CrossRef] [PubMed]
  199. Dockrell, D.H. Human Herpesvirus 6: Molecular Biology and Clinical Features. J. Med. Microbiol. 2003, 52, 5–18. [Google Scholar] [CrossRef]
  200. Jones, J.L.; Hanson, D.L.; Dworkin, M.S.; Jaffe, H.W. Incidence and Trends in Kaposi’s Sarcoma in the Era of Effective Antiretroviral Therapy. J. Acquir. Immune Defic. Syndr. 2000, 24, 270–274. [Google Scholar] [CrossRef]
  201. Rimland, D.; Moanna, A. Increasing Incidence of Herpes Zoster among Veterans. Clin. Infect. Dis. Off. Publ. Infect. Dis. Soc. Am. 2010, 50, 1000–1005. [Google Scholar] [CrossRef]
  202. Locksley, R.M.; Flournoy, N.; Sullivan, K.M.; Meyers, J.D. Infection with Varicella-Zoster Virus after Marrow Transplantation. J. Infect. Dis. 1985, 152, 1172–1181. [Google Scholar] [CrossRef]
  203. Niederman, J.C.; Miller, G.; Pearson, H.A.; Pagano, J.S.; Dowaliby, J.M. Infectious Mononucleosis. Epstein-Barr-Virus Shedding in Saliva and the Oropharynx. N. Engl. J. Med. 1976, 294, 1355–1359. [Google Scholar] [CrossRef]
  204. Burns, W.H.; Sandford, G.R. Susceptibility of Human Herpesvirus 6 to Antivirals in Vitro. J. Infect. Dis. 1990, 162, 634–637. [Google Scholar] [CrossRef] [PubMed]
  205. Tommasi, C.; Breuer, J. The Biology of Varicella-Zoster Virus Replication in the Skin. Viruses 2022, 14, 982. [Google Scholar] [CrossRef] [PubMed]
  206. Yang, F.; Yu, S.; Fan, B.; Liu, Y.; Chen, Y.; Kudel, I.; Concialdi, K.; DiBonaventura, M.; Hopps, M.; Hlavacek, P.; et al. The Epidemiology of Herpes Zoster and Postherpetic Neuralgia in China: Results from a Cross-Sectional Study. Pain. Ther. 2019, 8, 249–259. [Google Scholar] [CrossRef] [PubMed]
  207. Weller, T.H.; Witton, H.M.; Bell, E.J. The Etiologic Agents of Varicella and Herpes Zoster; Isolation, Propagation, and Cultural Characteristics in Vitro. J. Exp. Med. 1958, 108, 843–868. [Google Scholar] [CrossRef] [PubMed]
  208. Inchingolo, A.M.; Patano, A.; Di Pede, C.; Inchingolo, A.D.; Palmieri, G.; de Ruvo, E.; Campanelli, M.; Buongiorno, S.; Carpentiere, V.; Piras, F.; et al. Autologous Tooth Graft: Innovative Biomaterial for Bone Regeneration. Tooth Transformer® and the Role of Microbiota in Regenerative Dentistry. A Systematic Review. J. Funct. Biomater. 2023, 14, 132. [Google Scholar] [CrossRef]
  209. Inchingolo, A.D.; Carpentiere, V.; Piras, F.; Netti, A.; Ferrara, I.; Campanelli, M.; Latini, G.; Viapiano, F.; Costa, S.; Malcangi, G.; et al. Orthodontic Surgical Treatment of Impacted Mandibular Canines: Systematic Review and Case Report. Appl. Sci. 2022, 12, 8008. [Google Scholar] [CrossRef]
  210. Inchingolo, A.D.; Gargiulo, C.I.; Malcangi, G.; Ciocia, A.M.; Patano, A.; Azzollini, D.; Piras, F.; Barile, G.; Settanni, V.; Mancini, A.; et al. Diagnosis of SARS-CoV-2 during the Pandemic by Multiplex RT-rPCR hCoV Test: Future Perspectives. Pathogens 2022, 11, 1378. [Google Scholar] [CrossRef]
  211. Inchingolo, A.M.; Malcangi, G.; Inchingolo, A.D.; Mancini, A.; Palmieri, G.; Di Pede, C.; Piras, F.; Inchingolo, F.; Dipalma, G.; Patano, A. Potential of Graphene-Functionalized Titanium Surfaces for Dental Implantology: Systematic Review. Coatings 2023, 13, 725. [Google Scholar] [CrossRef]
  212. Inchingolo, A.D.; Malcangi, G.; Ceci, S.; Patano, A.; Corriero, A.; Vimercati, L.; Azzollini, D.; Marinelli, G.; Coloccia, G.; Piras, F.; et al. Effectiveness of SARS-CoV-2 Vaccines for Short- and Long-Term Immunity: A General Overview for the Pandemic Contrast. Int. J. Mol. Sci. 2022, 23, 8485. [Google Scholar] [CrossRef]
  213. Patano, A.; Malcangi, G.; De Santis, M.; Morolla, R.; Settanni, V.; Piras, F.; Inchingolo, A.D.; Mancini, A.; Inchingolo, F.; Dipalma, G.; et al. Conservative Treatment of Dental Non-Carious Cervical Lesions: A Scoping Review. Biomedicines 2023, 11, 1530. [Google Scholar] [CrossRef]
Figure 1. PRISMA flowchart of the literature search and article inclusion process.
Figure 1. PRISMA flowchart of the literature search and article inclusion process.
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Figure 2. Bias assessment by Robins tool [14,17,18,48,50,51,54,55,56,57,58,59].
Figure 2. Bias assessment by Robins tool [14,17,18,48,50,51,54,55,56,57,58,59].
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Figure 3. Preoperative clinical view. (A) Extraoral view. (B) Intraoral view.
Figure 3. Preoperative clinical view. (A) Extraoral view. (B) Intraoral view.
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Figure 4. Preoperative radiographs. (A) Preoperative panoramic view. (B) Pre-operative computed tomography sagittal view. (C) Pre-operative computed tomography axial view. (D) Pre-operative computed tomography frontal view.
Figure 4. Preoperative radiographs. (A) Preoperative panoramic view. (B) Pre-operative computed tomography sagittal view. (C) Pre-operative computed tomography axial view. (D) Pre-operative computed tomography frontal view.
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Figure 5. Intraoperative procedures. (A) Sequestrectomy and teeth removal were conducted. (B) Fragments of necrotic bone. (C) A sound bone bed was exposed and primarily closed.
Figure 5. Intraoperative procedures. (A) Sequestrectomy and teeth removal were conducted. (B) Fragments of necrotic bone. (C) A sound bone bed was exposed and primarily closed.
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Figure 6. Postoperative examinations. (A) Postoperative panoramic view. (B) Intraoral view.
Figure 6. Postoperative examinations. (A) Postoperative panoramic view. (B) Intraoral view.
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Table 1. Indicators for database searches.
Table 1. Indicators for database searches.
Articles screening strategyKEYWORDS: “A”: Herpes Zoster; “B”: osteonecros*;
Boolean Indicators: “A” AND “B”
Timespan: 1 January 2004, to 7 June 2024
Electronic databases: PubMed; Scopus; Web of Science.
Table 2. A descriptive item selection summary.
Table 2. A descriptive item selection summary.
Authors (Year of Publication)Type of StudyAim of the StudyMaterialsResults
Emilie Faure et al. (2022) [51]Case reportTo report a rare case of mandibular osteonecrosis following HZ infection and review relevant literature.87-year-old Caucasian man affected by uncontrolled diabetes (HbA1c: 8.8%), complicated by microangiopathy and macroangiopathy, myocardial infarction, and integrative omics-metabolic analysis (IOMA) that required a femoral bypass. Reported discomfort in wearing his prosthesis, responsible for feeding difficulties. Intraoral examination revealed a large bone exposure in the previously ulcerated area, measuring 2 cm × 1 cm, and showing necrotic alveolar bone associated with peripheral suppuration.Osteonecrosis of the right mandibular alveolus was identified; it was treated with antibiotics, extraction of the tooth, and excision of necrotic bone. Intermaxillary fixation and a titanium reconstruction plate were used to manage the following pathological fracture, and a follow-up revealed satisfactory bone healing.
Maojia Yin et al. (2022) [18]Case report and literature reviewTo review the literature, report a case of HZ, and cause mandibular alveolar bone necrosis.A 50-year-old man who requested pain medication for facial and ear pain also developed necrosis, blister rash, hearing loss, and facial paralysis.Trigeminal HZ and RHS were identified after tumors and other infectious illnesses were ruled out.
Travis Rudd et al. (2021) [53]Case report and literature reviewDescribe a case of mandibular alveolar bone necrosis and Ramsay Hunt Syndrome that occurred after HZ and review relevant literature.HZ affecting the mandibular branch of the trigeminal nerve manifested in a 59-year-old male with a medical history that included hypertension, hyperlipidemia, and granulomatosis with polyangiitis (Wegener). He also experienced impaired hearing in his right ear as a result of Ramsay Hunt Syndrome (RHS) and peripheral Bell palsy on the right side. Spontaneous tooth loss and osteonecrosis in the right mandible, which were linked to a severe case of facial HZ rash and ongoing RHS symptoms.The case emphasized the prevalence of mandibular osteonecrosis and Ramsay Hunt Syndrome post-HZ; treatment included antiviral and antibiotic medication, leading to clinical improvement.
Samprati J Badjate et al. (2020) [17]Case report and literature reviewReviewing the relevant literature and reporting an unusual case of Ramsay Hunt Syndrome aggravated by edentulous maxilla and mandible osteonecrosis.An 86-year-old patient with facial nerve paralysis post HZI, edentulous arches, fibrosis, tongue depapillation, white scarring, blood-encrusted areas, low-grade lower motor neuron facial palsy, and exposed alveolar bone.The therapy of Ramsay Hunt Syndrome and related osteonecrosis was described in depth in the case report. Significant clinical improvement resulted from the use of antibiotics and antiviral medication during treatment.
Kaikai Huang et al. (2024) [54]Case report and literature reviewTo investigate how infection contributes to the development of alveolar osteonecrosis after zoster facial herpes.A 67-year-old man experienced facial hemorrhage and alveolar osteonecrosis.The study suggested that infection might significantly contribute to the development of alveolar osteonecrosis post-HZ. The case report detailed diagnosis and treatment with antibiotics and antiviral therapy, showing positive outcomes.
Aritra Chatterjee et al. (2023) [55]Case reportTo describe and elaborate on a delayed case of HZI that resulted in mandibular osteonecrosis.Following three months of HZI, a 51-year-old male patient showed signs of spontaneous exfoliation of several teeth and a subsequent pathological fracture on the right side of the lower jaw.No signs of recurrence were seen throughout the patient’s year-long follow-up.
Osteonecrosis after heart-lung transplantation is a distinct but uncommon presentation that needs to be recognized right away.
Garima S. (2020) [56]Case report and literature reviewTo highlight the importance of early diagnosis and appropriate management of the condition, as well as the need for a detailed medical and dental history to facilitate timely intervention.The subject of the study is a 13-year-old patient who presented with a rare condition associated with HZI. Specifically, the patient experienced alveolar osteonecrosis and tooth exfoliation, which are uncommon oral complications of HZ, particularly in pediatric patients.The patient underwent symptomatic pharmacological therapy for a week, with an improvement in symptoms. A prosthetic rehabilitation was performed with a removable partial denture for tooth 11.
Jae-Min S. (2015) [50]Case report and literature reviewThe study aims to highlight the rare but significant dental complications associated with HZ infection, particularly in the mandibular branch, and to discuss the management and treatment options.The subject of the study is a 64-year-old male patient who presented with osteonecrosis with bone exposure in the left mandible as a complication of HZ infection involving the mandibular branch of the trigeminal nerve.The treatment with sequestrectomy and removal of teeth 31–35 was successfully performed, and, during the follow-up period, there were no further episodes of tooth loss, bone exposure, or osteonecrosis, nor complications such as postherpetic neuralgia.
Mendieta C. (2005) [57]Case report and literature reviewTo discuss the clinical manifestations, treatment, and potential mechanisms underlying this rare complication of HZ infection.A 63-year-old woman with HZ infection involving the trigeminal nerve with advanced alveolar bone loss observed around teeth 27 and 28.The patient was treated with oral and topical acyclovir, carbamazepine, amoxicillin, and chlorhexidine digluconate. Teeth 27 and 28 were extracted due to hopeless prognosis. Fragments of necrotic alveolar bone were removed.
Kamala G.P. (2006) [14]Case reportTo present a case report of trigeminal HZ infection affecting the left maxillary and ophthalmic divisions of the fifth cranial nerve in an immunocompetent patient. A 34-year-old male presented with a diagnosis of HZ in the ophthalmic and maxillary nerve, complicated by alveolar bone necrosis.The patient was treated with aciclovir, erythromycin stearate, and ophthalmic medications. The patient responded favorably to the dental treatment and reported progressive improvement in vision in his left eye.
Florence E.C. (2013) [58]Case report and literature reviewTo evaluate the safety and efficacy of azathioprine in HIV-infected individuals, focusing on potential adverse events, immune parameters, and hemoglobin levels. Four females and three males with a mean age of 38. All patients were receiving highly active antiretroviral therapy (HAART). Thiopurine methyltransferase activity was tested prior to commencing treatment with azathioprine, and all individuals were assessed as tolerant.The study concludes that azathioprine can be used in HIV-infected individuals with careful monitoring of immune parameters and hemoglobin levels. No serious opportunistic infections or malignancies were reported.
Rupinder K. (2016) [48]Case report and literature reviewTo report a rare case of spontaneous tooth exfoliation associated with trigeminal HZ in a diabetic patient.A 47-year-old male with crusty lesions of herpes infection over the left side of the face and high mobility in the left upper central incisor that subsequently exfoliated. Spontaneous tooth exfoliation is a rare but significant complication of trigeminal HZ, particularly in patients with underlying diabetes mellitus.
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Mancini, A.; Chirico, F.; Inchingolo, A.M.; Piras, F.; Colonna, V.; Marotti, P.; Carone, C.; Inchingolo, A.D.; Inchingolo, F.; Dipalma, G. Osteonecrosis of the Jaws Associated with Herpes Zoster Infection: A Systematic Review and a Rare Case Report. Microorganisms 2024, 12, 1506. https://doi.org/10.3390/microorganisms12081506

AMA Style

Mancini A, Chirico F, Inchingolo AM, Piras F, Colonna V, Marotti P, Carone C, Inchingolo AD, Inchingolo F, Dipalma G. Osteonecrosis of the Jaws Associated with Herpes Zoster Infection: A Systematic Review and a Rare Case Report. Microorganisms. 2024; 12(8):1506. https://doi.org/10.3390/microorganisms12081506

Chicago/Turabian Style

Mancini, Antonio, Fabrizio Chirico, Angelo Michele Inchingolo, Fabio Piras, Valeria Colonna, Pierluigi Marotti, Claudio Carone, Alessio Danilo Inchingolo, Francesco Inchingolo, and Gianna Dipalma. 2024. "Osteonecrosis of the Jaws Associated with Herpes Zoster Infection: A Systematic Review and a Rare Case Report" Microorganisms 12, no. 8: 1506. https://doi.org/10.3390/microorganisms12081506

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