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Keywords = vulvar lichen planus

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20 pages, 1791 KB  
Review
Squamous Cell Carcinoma In Situ—The Importance of Early Diagnosis in Bowen Disease, Vulvar Intraepithelial Neoplasia, Penile Intraepithelial Neoplasia, and Erythroplasia of Queyrat
by Lucian G. Scurtu, Francesca Scurtu, Sebastian Catalin Dumitrescu and Olga Simionescu
Diagnostics 2024, 14(16), 1799; https://doi.org/10.3390/diagnostics14161799 - 16 Aug 2024
Cited by 5 | Viewed by 9464
Abstract
Cutaneous squamous cell carcinoma (cSCC) is the second-most-prevalent malignancy in humans. A delayed diagnosis of cSCC leads to heightened invasiveness and positive surgical margins. Bowen’s disease (BD) represents an early form of cSCC and presents as a small erythematous, photo-distributed, psoriasiform plaque. Although [...] Read more.
Cutaneous squamous cell carcinoma (cSCC) is the second-most-prevalent malignancy in humans. A delayed diagnosis of cSCC leads to heightened invasiveness and positive surgical margins. Bowen’s disease (BD) represents an early form of cSCC and presents as a small erythematous, photo-distributed, psoriasiform plaque. Although certain dermoscopy features in BD are quite characteristic, histopathology remains the gold standard for diagnosis and provides a severity-scoring system that assists in guiding appropriate treatment strategies. The classification of precancerous lesions of the vulva and penis has undergone multifarious transformations due to variations in clinical and histopathological characteristics. Presently, erythroplasia of Queyrat is categorized as a clinical variant of penile intraepithelial neoplasia (PeIN). The diagnoses of vulvar intraepithelial neoplasia (VIN) and PeIN present significant challenges and typically necessitate one or more biopsies, potentially guided by dermoscopy. Aceto-white testing demonstrates a notably high negative predictive value for genital precancerous lesions. Histopathological examination represents the gold-standard diagnosis in VIN and PeIN, while p16 and p53 immunostainings alongside HPV testing provide crucial diagnostic clues. The histopathologic features, degree of differentiation, and associations with lichen planus, lichen sclerosus, and HPV guide the selection of conservative treatments or surgical excision. Full article
(This article belongs to the Special Issue New Developments in the Diagnosis of Skin Tumors)
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6 pages, 1793 KB  
Case Report
Vulvar Lichen Planus Presenting as Chronic Vulvar Purpura
by Boštjan Luzar, Anamarija Truden, Lara Turk, Vid Janša, Fiona Lewis, Eduardo Calonje and Špela Smrkolj
Medicina 2023, 59(2), 206; https://doi.org/10.3390/medicina59020206 - 20 Jan 2023
Cited by 1 | Viewed by 2398
Abstract
Background: There is a broad spectrum of vulvar pigmented lesions that differ based on their histopathological and clinical features. Chronic vulvar purpura is a rare entity, associated with a broad morphological spectrum, from lichen aureus, Zoon’s vulvitis, pigmented purpuric dermatosis and with [...] Read more.
Background: There is a broad spectrum of vulvar pigmented lesions that differ based on their histopathological and clinical features. Chronic vulvar purpura is a rare entity, associated with a broad morphological spectrum, from lichen aureus, Zoon’s vulvitis, pigmented purpuric dermatosis and with lichen planus as in our case. Case presentation: In this article we discuss a case of an 86-year-old white woman with hyperpigmentation on her upper vulva, next to the introitus, with complaints of urine incontinence. Biopsy revealed subepithelial stromal lichenoid inflammatory infiltrate containing plasma cells, lymphocytes and some neutrophilic granulocytes as well as dilated and congested vessels. Hemosiderin deposits and erythrocyte extravasation were found. There was evidence of hyperkeratosis with hyper granulosis and erosions. Spongiosis was also noted. Few melanocytes were identified with no sign of malignancy. These findings correlate with the diagnosis of vulvar lichen planus. Conclusions: Chronic vulvar purpura is a clinical term used for different chronic inflammatory dermatoses presenting as red bluish or violaceous discolorations on the vulva, often associated with cayenne-pepper-like speckling. Considering a great overlap of possible diseases, the final diagnosis could be challenging. It is important to exclude a melanocytic tumour in these cases. Full article
(This article belongs to the Section Dermatology)
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23 pages, 2516 KB  
Systematic Review
How Can We Treat Vulvar Carcinoma in Pregnancy? A Systematic Review of the Literature
by Andrea Palicelli, Lucia Giaccherini, Magda Zanelli, Maria Paola Bonasoni, Maria Carolina Gelli, Alessandra Bisagni, Eleonora Zanetti, Loredana De Marco, Federica Torricelli, Gloria Manzotti, Mila Gugnoni, Giovanni D’Ippolito, Angela Immacolata Falbo, Filomena Giulia Sileo, Lorenzo Aguzzoli, Valentina Mastrofilippo, Martina Bonacini, Federica De Giorgi, Stefano Ricci, Giuditta Bernardelli, Laura Ardighieri, Maurizio Zizzo, Antonio De Leo, Giacomo Santandrea, Dario de Biase, Moira Ragazzi, Giulia Dalla Dea, Claudia Veggiani, Laura Carpenito, Francesca Sanguedolce, Aleksandra Asaturova, Renzo Boldorini, Maria Giulia Disanto, Margherita Goia, Richard Wing-Cheuk Wong, Naveena Singh and Vincenzo Dario Mandatoadd Show full author list remove Hide full author list
Cancers 2021, 13(4), 836; https://doi.org/10.3390/cancers13040836 - 17 Feb 2021
Cited by 17 | Viewed by 4065
Abstract
According to our systematic literature review (PRISMA guidelines), only 37 vulvar squamous cell carcinomas (VSCCs) were diagnosed during pregnancy (age range: 17–41 years). The tumor size range was 0.3–15 cm. The treatment was performed after (14/37, 38%), before (10/37, 27%), or before-and-after delivery [...] Read more.
According to our systematic literature review (PRISMA guidelines), only 37 vulvar squamous cell carcinomas (VSCCs) were diagnosed during pregnancy (age range: 17–41 years). The tumor size range was 0.3–15 cm. The treatment was performed after (14/37, 38%), before (10/37, 27%), or before-and-after delivery (11/37, 30%). We found that 21/37 (57%) cases were stage I, 2 II (5%), 11 III (30%), and 3 IVB (8%). HPV-related features (condylomas/warts; HPV infection; high-grade squamous intraepithelial lesion) were reported in 11/37 (30%) cases. We also found that 9/37 (24%) patients had inflammatory conditions (lichen sclerosus/planus, psoriasis, chronic dermatitis). The time-to-recurrence/progression (12/37, 32%) ranged from 0 to 36 (mean 9) months. Eight women died of disease (22%) 2.5–48 months after diagnosis, 2 (5%) were alive with disease, and 23 (62%) were disease-free at the end of follow-up. Pregnant patients must be followed-up. Even if they are small, newly arising vulvar lesions should be biopsied, especially in women with risk factors (HPV, dermatosis, etc.). The treatment of VSCCs diagnosed in late third trimester might be delayed until postpartum. Elective cesarean section may prevent vulvar wound dehiscence. In the few reported cases, pregnancy/fetal outcomes seemed to not be affected by invasive treatments during pregnancy. However, clinicians must be careful; larger cohorts should define the best treatment. Definite guidelines are lacking, so a multidisciplinary approach and discussion with patients are mandatory. Full article
(This article belongs to the Special Issue Cancer and Pregnancy)
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