Clinical Diagnosis and Treatment of Vasculitis and Arteritis

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Immunology".

Deadline for manuscript submissions: closed (2 May 2024) | Viewed by 673

Special Issue Editor


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Guest Editor
Clinica Medica, Dipartimento di Scienze Cliniche e Molecolari, Università Politecnica delle Marche, Via Tronto 10/A, 60126 Ancona, AN, Italy
Interests: autoimmunity; vasculitis; connective tissue diseases; rare diseases; immunology; haematology; rheumatology; target therapies

Special Issue Information

Dear Colleagues,

The term “vasculitis” refers to a heterogeneous group of disorders characterized by the inflammatory damage of blood vessel walls with deterioration of vessel integrity and impairment of the lumen.

Vasculitis is, conventionally, classified into large-vessel, medium-vessel, and small-vessel vasculitis according to the size of the affected vessels, mainly arteries or capillaries.

This inflammatory process may lead to hemorrhagic or ischemic consequences, with different clinical manifestations and prognoses. Most of them are systemic disorders, potentially involving any organ and system, but there is also vasculitis affecting a single organ or single vessel.

Vasculitis presents a wide spectrum of clinical manifestations, from being a self-limiting disorder to a life-threatening systemic disease, with a relevant burden of morbidity and mortality, according to the pathogenesis and size of the vessel involved.

Vasculitis is generally considered a rare disease, but probably only when considered singularly.

In recent years many advances in pathophysiology, diagnosis, and therapy have been attained.

The most impressive results have been obtained with the incoming new biologic immunosuppressive or immunomodulating agents (rituximab, tocilizumab, belimumab, anti-IL5, and anti-TNF agents), allowing for less use of corticosteroids and classical cytostatic immunosuppressive agents (e.g., cyclophosphamide and methotrexate).

Furthermore, the introduction of PET/CT and PET/MRI techniques or non-invasive novel angiography techniques has supplied irreplaceable diagnostic tools.

This Special Issue, “Clinical Diagnosis and Treatment of Vasculitis and Arteritis”, aims to provide in-depth insights into the latest developments in diagnosing and treating these conditions. Researchers and experts in the field would contribute with articles covering various aspects of vasculitis and arteritis, including advances in diagnostic techniques, such as imaging and biomarkers, and treatment options, including new medication regimens and immunosuppressive therapies. Nonetheless, original articles and research reviews are welcomed.

Dr. Paolo Fraticelli
Guest Editor

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Keywords

  • vasculitis
  • arteritis
  • diagnosis
  • treatment
  • autoimmunity
  • biologic therapies

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Published Papers (1 paper)

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19 pages, 11928 KiB  
Review
Cocaine- and Levamisole-Induced Vasculitis: Defining the Spectrum of Autoimmune Manifestations
by Luca Iorio, Federica Davanzo, Diego Cazzador, Marta Codirenzi, Eleonora Fiorin, Elisabetta Zanatta, Piero Nicolai, Andrea Doria and Roberto Padoan
J. Clin. Med. 2024, 13(17), 5116; https://doi.org/10.3390/jcm13175116 - 28 Aug 2024
Viewed by 417
Abstract
Drug-induced or associated vasculitis is a prevalent form of vasculitis that resembles primary idiopathic antineutrophil cytoplasmic autoantibody (ANCA) vasculitis (AAV). Cocaine is a diffuse psychostimulant drug and levamisole is a synthetic compound used to cut cocaine. Their abuse may result in a spectrum [...] Read more.
Drug-induced or associated vasculitis is a prevalent form of vasculitis that resembles primary idiopathic antineutrophil cytoplasmic autoantibody (ANCA) vasculitis (AAV). Cocaine is a diffuse psychostimulant drug and levamisole is a synthetic compound used to cut cocaine. Their abuse may result in a spectrum of autoimmune manifestations which could be categorized into three overlapping clinical pictures: cocaine-induced midline destructive lesion (CIMDL), levamisole-adulterated cocaine (LAC) vasculopathy/vasculitis, and cocaine-induced vasculitis (CIV). The mechanisms by which cocaine use leads to disorders resembling AAV are not well understood. Cocaine can cause autoimmune manifestations ranging from localized nasal lesions to systemic diseases, with neutrophils playing a key role through NETosis and ANCA development, which exacerbates immune responses and tissue damage. Diagnosing and treating these conditions becomes challenging when cocaine and levamisole abuse is not suspected, due to the differences and overlaps in clinical, diagnostic, therapeutic, and prognostic aspects compared to primary idiopathic vasculitides. Full article
(This article belongs to the Special Issue Clinical Diagnosis and Treatment of Vasculitis and Arteritis)
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