Leukocytoclastic Vasculitis as an Extraintestinal Manifestation of Crohn's Disease

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Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.contributorClinica Universidad de Los Andes-
Autor(es): dc.creatorRocha, Thiara Barcelos-
Autor(es): dc.creatorGarate, Ana Lorena Sousa De Vasconcelos-
Autor(es): dc.creatorBeraldo, Rodrigo Fedatto-
Autor(es): dc.creatorLanças, Sean Hideo Shirata-
Autor(es): dc.creatorLeite, Fábio Vicente-
Autor(es): dc.creatorQuera, Rodrigo-
Autor(es): dc.creatorBarros, Jaqueline Ribeiro-
Autor(es): dc.creatorBaima, Julio Pinheiro-
Autor(es): dc.creatorSaad-Hossne, Rogerio-
Autor(es): dc.creatorSassaki, Ligia Yukie-
Data de aceite: dc.date.accessioned2025-08-21T22:56:15Z-
Data de disponibilização: dc.date.available2025-08-21T22:56:15Z-
Data de envio: dc.date.issued2022-05-01-
Data de envio: dc.date.issued2022-05-01-
Data de envio: dc.date.issued2020-12-31-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1159/000519003-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/233652-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/233652-
Descrição: dc.descriptionCutaneous involvement is one of the most common extraintestinal manifestations of inflammatory bowel disease (IBD). More commonly, pyoderma gangrenosum and erythema nodosum are noted, but psoriasis, aphthous stomatitis, Sweet's syndrome, and vasculitis may also occur. Leukocytoclastic vasculitis (LCV) is a rare cutaneous manifestation, characterized by the appearance of palpable purpura, urticaria, and ulcer-necrotic lesions predominantly in the lower extremities that improve with immunosuppressive therapy. In this case, we report a patient with CD and LCV. We also searched the literature on the diagnosis and treatment of LCV in patients with CD. Female, 31, presented with diarrhea containing mucus and blood, abdominal pain, arthralgia, and enanthematous plaques and ulcers with a hematinic background in the lower extremities. The results of the colonoscopy were compatible with CD and skin biopsy showed signs of LCV. Systemic autoimmune disease and primary vasculitis were ruled out. The patient received treatment with a systemic corticosteroid and the skin lesions improved. Outpatient treatment with antitumor necrosis factor therapy was initiated to promote skin healing and IBD clinical remission. As LCV is a rare manifestation of IBD, it is necessary to distinguish this dermatopathy from other systemic vasculitis. The engagement of a multidisciplinary team is essential for the correct diagnosis and management.-
Descrição: dc.descriptionSão Paulo State University (Unesp) Medical School-
Descrição: dc.descriptionClinica Universidad de Los Andes-
Descrição: dc.descriptionSão Paulo State University (Unesp) Medical School-
Formato: dc.format825-831-
Idioma: dc.languageen-
Relação: dc.relationCase Reports in Gastroenterology-
???dc.source???: dc.sourceScopus-
Palavras-chave: dc.subjectCase report-
Palavras-chave: dc.subjectCrohn's disease-
Palavras-chave: dc.subjectExtraintestinal manifestation-
Palavras-chave: dc.subjectInflammatory bowel disease-
Palavras-chave: dc.subjectLeukocytoclastic vasculitis-
Título: dc.titleLeukocytoclastic Vasculitis as an Extraintestinal Manifestation of Crohn's Disease-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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