Systemic Lupus Erythematosus Simulating Kikuchi Fujimoto’s Disease: A Case Report

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Kikuchi–Fujimoto disease and systemic lupus erythematosus

Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is an infrequent idiopathic disorder. It has been associated with autoimmune disorders, of which systemic lupus erythematosus is the most outstanding. The basis of its diagnosis relies on the histological examination of lymph nodes, which typically reveals necrosis surrounded by histiocytes with crescentic nucleus, immunoblasts...

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A Case of Systemic Lupus Erythematosus

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Kikuchi Fujimoto Disease with Rare Demonstrations Associated with Lupus Erythematosus without Obvious Clinical Symptoms: A Case Report

Kikuchi Fujimoto Disease (KFD), also known as necrotic histiocystic lymphadenitis, is a condition with unknown etiology. Probably, infectious, viral, and also autoimmune etiologies, especially lupus erythematosus, contribute to this disorder. The common signs are lymphadenopathy along with fever and leukopenia. Our case was a13-year-old boy with fever of unknown origin. He underwent ordinary fe...

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[Kikuchi-Fujimoto disease prior to childhood-systemic lupus erythematosus diagnosis].

Kikuchi-Fujimoto disease (KFD) is a self-limiting histiocytic necrotizing lymphadenitis of unknown origin. Of note, KFD was infrequently reported in adult systemic lupus erythematosus (SLE), with rare occurrence in childhood-SLE (C-SLE) patients. To our knowledge, the prevalence of KFD in the paediatric lupus population was not studied. Therefore, in a period of 29 consecutive years, 5,682 pati...

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ژورنال

عنوان ژورنال: Journal of Bangladesh College of Physicians and Surgeons

سال: 2015

ISSN: 1015-0870

DOI: 10.3329/jbcps.v32i4.26112