SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT

Systemic vasculitides (SV) are a heterogeneous group of acute and chronic diseases, the most important pathomorphological sign of which is inflammation and necrosis of the vascular wall. The basis for the classification of SV is their etiology and pathogenesis, the type of affected vessels and the p...

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Main Authors: N. A. Shostak, A. A. Klimenko
Format: Article
Language:Russian
Published: ABV-press 2015-08-01
Series:Klinicist
Subjects:
Online Access:https://klinitsist.abvpress.ru/Klin/article/view/189
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author N. A. Shostak
A. A. Klimenko
author_facet N. A. Shostak
A. A. Klimenko
author_sort N. A. Shostak
collection DOAJ
description Systemic vasculitides (SV) are a heterogeneous group of acute and chronic diseases, the most important pathomorphological sign of which is inflammation and necrosis of the vascular wall. The basis for the classification of SV is their etiology and pathogenesis, the type of affected vessels and the pattern of inflammation, predominant organ involvements, clinical manifestations, a genetic predisposition, and demographic characteristics. To diagnose vasculitis is a difficult task due to a broad spectrum of its clinical manifestations that depend on the predominant size of affected vessels, the involved organs and systems, and the magnitude of the inflammatory process. There are no specific laboratory tests for most forms of SV; nonspecific inflammatory measures and activated autoimmune reactions are noted to be higher. Screening for SV determines the levels of anti-neutrophil cytoplasmic antibodies (ANCA), cryoglobulins, anti-glomerular basement membrane antibodies, and anti-complement C1q antibodies. However, biopsy with its specimen being pathomorphologically characterized, as well as current noninvasive or minimally invasive diagnostic techniques remain relevant because of a large number of seronegative variants of vasculitis. The ANCA-associated vasculitis management algorithm developed by the British Society of Rheumatology has been presented in 2015. The timely diagnosis and treatment at the onset of SV is the basis for quality of life and survival improvement.
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spelling doaj.art-ea4d2c6057984684b625b3a2232aff612025-03-05T14:05:11ZrusABV-pressKlinicist1818-83382015-08-019281210.17650/1818-8338-2015-9-2-8-12190SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENTN. A. Shostak0A. A. Klimenko1Acad. A.I. Nesterov Department of Faculty Therapy, N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia; 1 Ostrovityanova St., Moscow, 117997, RussiaAcad. A.I. Nesterov Department of Faculty Therapy, N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia; 1 Ostrovityanova St., Moscow, 117997, RussiaSystemic vasculitides (SV) are a heterogeneous group of acute and chronic diseases, the most important pathomorphological sign of which is inflammation and necrosis of the vascular wall. The basis for the classification of SV is their etiology and pathogenesis, the type of affected vessels and the pattern of inflammation, predominant organ involvements, clinical manifestations, a genetic predisposition, and demographic characteristics. To diagnose vasculitis is a difficult task due to a broad spectrum of its clinical manifestations that depend on the predominant size of affected vessels, the involved organs and systems, and the magnitude of the inflammatory process. There are no specific laboratory tests for most forms of SV; nonspecific inflammatory measures and activated autoimmune reactions are noted to be higher. Screening for SV determines the levels of anti-neutrophil cytoplasmic antibodies (ANCA), cryoglobulins, anti-glomerular basement membrane antibodies, and anti-complement C1q antibodies. However, biopsy with its specimen being pathomorphologically characterized, as well as current noninvasive or minimally invasive diagnostic techniques remain relevant because of a large number of seronegative variants of vasculitis. The ANCA-associated vasculitis management algorithm developed by the British Society of Rheumatology has been presented in 2015. The timely diagnosis and treatment at the onset of SV is the basis for quality of life and survival improvement.https://klinitsist.abvpress.ru/Klin/article/view/189systemic vasculitisclassificationgiant-cell arteritisanti-neutrophil cytoplasmic antibodiesanti-neutrophil cytoplasmic antibodies vasculitisautoantibodiesanti-glomerular basement membrane antibodiesmanagement algorithmmethotrexateazathio
spellingShingle N. A. Shostak
A. A. Klimenko
SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
Klinicist
systemic vasculitis
classification
giant-cell arteritis
anti-neutrophil cytoplasmic antibodies
anti-neutrophil cytoplasmic antibodies vasculitis
autoantibodies
anti-glomerular basement membrane antibodies
management algorithm
methotrexate
azathio
title SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
title_full SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
title_fullStr SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
title_full_unstemmed SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
title_short SYSTEMIC VASCULITIS: NOVELTY IN CLASSIFICATION, DIAGNOSIS, AND TREATMENT
title_sort systemic vasculitis novelty in classification diagnosis and treatment
topic systemic vasculitis
classification
giant-cell arteritis
anti-neutrophil cytoplasmic antibodies
anti-neutrophil cytoplasmic antibodies vasculitis
autoantibodies
anti-glomerular basement membrane antibodies
management algorithm
methotrexate
azathio
url https://klinitsist.abvpress.ru/Klin/article/view/189
work_keys_str_mv AT nashostak systemicvasculitisnoveltyinclassificationdiagnosisandtreatment
AT aaklimenko systemicvasculitisnoveltyinclassificationdiagnosisandtreatment