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Type: Artigo
Title: Panniculitis in childhood-onset systemic lupus erythematosus : a multicentric cohort study
Author: Verdier, Mônica
Anuardo, Pedro
Gormezano, Natali Weniger Spelling
Romiti, Ricardo
Campos, Lucia Maria Arruda
Aikawa, Nadia Emi
Pereira, Rosa Maria Rodrigues
Terreri, Maria Teresa
Magalhães, Claudia Saad
Ferreira, Juliana C. O. A.
Silva, Marco Felipe Castro
Ferriani, Mariana
Sakamoto, Ana Paula
Ferriani, Virginia Paes Leme
Centeville, Maraísa
Sato, Juliana
Santos, Maria Carolina
Bonfá, Eloisa
Silva, Clovis Artur
Abstract: To evaluate prevalence, clinical manifestations, laboratory abnormalities, treatment and outcome in a multicenter cohort of childhood-onset systemic lupus erythematosus (cSLE) patients with and without panniculitis. Panniculitis was diagnosed due to painful subcutaneous nodules and/or plaques in deep dermis/subcutaneous tissues and lobular/mixed panniculitis with lymphocytic lobular inflammatory infiltrate in skin biopsy. Statistical analysis was performed using Bonferroni correction(p < 0.004). Panniculitis was observed in 6/847(0.7%) cSLE. Painful subcutaneous erythematosus and indurated nodules were observed in 6/6 panniculitis patients and painful subcutaneous plaques in 4/6. Generalized distribution was evidenced in 3/6 and localized in upper limbs in 2/6 and face in 1/6. Cutaneous hyperpigmentation and/or cutaneous atrophy occurred in 5/6. Histopathology features showed lobular panniculitis without vasculitis in 5/6(one of them had concomitant obliterative vasculopathy due to antiphospholipid syndrome) and panniculitis with vasculitis in 1/6. Comparison between cSLE with panniculitis and 60 cSLE without panniculitis with same disease duration [2.75(0–11.4) vs. 2.83(0–11.8) years,p = 0.297], showed higher frequencies of constitutional involvement (67% vs. 10%,p = 0.003) and leukopenia (67% vs. 7%,p = 0.002). Cutaneous atrophy and hyperpigmentation occurred in 83% of patients. Panniculitis is a rare skin manifestation of cSLE occurring in the first three years of disease with considerable sequelae. The majority of patients have concomitant mild lupus manifestations
Subject: Lúpus eritematoso sistêmico
Estudo multicêntrico
Country: Reino Unido
Editor: Springer Nature
Rights: Aberto
Identifier DOI: 10.1186/s42358-019-0049-9
Date Issue: 2019
Appears in Collections:FCM - Artigos e Outros Documentos

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