Systemic disease in leukocytoclastic vasculitis: a focus on direct immunofluorescence findings

dc.authorid0000-0002-7031-6516
dc.authorid0000-0002-0433-7669
dc.authorid0000-0003-0958-915X
dc.authorid0000-0003-4964-1741
dc.authorid0000-0002-3457-1958
dc.authorid0000-0002-6012-0528
dc.authorid0000-0002-6326-6178
dc.contributor.authorErtekin, Sumeyre Seda
dc.contributor.authorAksu, Ayse Esra Koku
dc.contributor.authorLeblebici, Cem
dc.contributor.authorErdemir, Vefa Asli
dc.contributor.authorErdem, Ozan
dc.contributor.authorAvci, Elif Bal
dc.contributor.authorGürel, Mehmet Salih
dc.date.accessioned2025-05-10T19:48:17Z
dc.date.issued2023
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground: Direct immunofluorescence (DIF) panels are usually ordered for clinically suspected cutaneous vasculitis, but their positivity rate is variable, and their prognostic significance is not clear to date. Objective: The study aims to investigate the systemic involvement rate in leukocytoclastic vasculitis (LCV) patients and the potential clinical and laboratory associations with systemic involvement, including DIF findings. Methods: A retrospective study of patients with histopathologically proven cutaneous LCV examined in the dermatology department between 2013 and 2017 was performed. Results: Of the 81 patients (mean age, 50.6 years), 42 (52%) were male. The mean time between the appearance of skin lesions and biopsy was 23.1 days, ranging from 2 to 180 days. DIF showed overall positivity of 90.1%, and C3 was the most frequent immunoreactant (82.7%). Any kind of extracutaneous involvement was present in 47 (58%) of patients, with renal involvement being the most frequent (53.1%), followed by articular (18.5%) and gastrointestinal (11.1%) involvement. The presence of renal disease was associated with the detection of IgG in the lesional skin (p = 0.017), and with the absence of IgM in the lesional skin (p = 0.032). There was a significant association between C3 deposition and joint involvement (p = 0.05). Study limitations: This is a single-center study with a retrospective design. Conclusion: DIF seems to be a useful ancillary diagnostic tool in the evaluation of cutaneous vasculitis, but the relationship between DIF findings and systemic involvement needs to be further elucidated due to contradictory data in the current literature. (c) 2022 Sociedade Brasileira de Dermatologia. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
dc.identifier.doi10.1016/j.abd.2021.11.009
dc.identifier.endpage67
dc.identifier.issn0365-0596
dc.identifier.issn1806-4841
dc.identifier.issue1
dc.identifier.pmid36369199
dc.identifier.scopus2-s2.0-85141499991
dc.identifier.scopusqualityQ2
dc.identifier.startpage59
dc.identifier.urihttps://doi.org/10.1016/j.abd.2021.11.009
dc.identifier.urihttps://hdl.handle.net/20.500.14730/11664
dc.identifier.volume98
dc.identifier.wosWOS:000925558200001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Science Inc
dc.relation.ispartofAnais Brasileiros De Dermatologia
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectFluorescent antibody technique
dc.subjectdirect
dc.subjectImmunoglobulin M
dc.subjectImmunoglobulin G
dc.subjectSystemic vasculitis
dc.subjectVasculitis
dc.subjectleukocytoclastic
dc.subjectcutaneous
dc.titleSystemic disease in leukocytoclastic vasculitis: a focus on direct immunofluorescence findings
dc.typeArticle

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