3.9 Article

Lymphadenopathy and systemic lupus erythematosus

Journal

REVISTA BRASILEIRA DE REUMATOLOGIA
Volume 50, Issue 1, Pages 99-101

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1590/S0482-50042010000300010

Keywords

systemic lupus erythematosus; fever of unknown origin; wasting syndrome; auto-antibodies; lymphadenopathy

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Lymphadenopathy is a benign finding in systemic lupus erythematosus (SLE), commonly seen in young patients with cutaneous involvement and constitutional symptoms, with good response to corticosteroids. Reactive follicular hyperplasia is the most frequent finding in biopsies. We report the case of a patient with recurrent episodes of lymphadenopathy associated with hepatosplenomegaly, fever, and weight loss since the age of 13 years. The patient also developed arthritis, hypertension, proteinuria, cardiomyopathy, and peripheral neuropathy. His condition was investigated extensively without diagnostic clarification; he was treated, empirically, for tuberculosis. The patient received a diagnosis of SLE only five years after the original presentation and received the specific treatment. Early diagnosis in those cases is difficult because laboratorial exams may not show the presence of auto-antibodies and low complement levels.

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