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复发性菊池-藤本病:病例报告

Recurrent Kikuchi-Fujimoto disease: case report.

作者信息

Sah Sunil K, Pant Ravi, Piper Kim, Chowdhury Tahseen A, Crean St John

机构信息

Department of Oral and Maxillofacial Surgery, Royal London Hospital, Whitechapel, London E1 1BB, UK.

出版信息

Br J Oral Maxillofac Surg. 2007 Apr;45(3):231-3. doi: 10.1016/j.bjoms.2005.07.021. Epub 2005 Dec 13.

Abstract

Kikuchi-Fujimoto disease, also known as histiocytic necrotising lymphadenitis, is a self-limiting condition of uncertain aetiology characterised by lymphadenopathy, pyrexia, and neutropenia. Some reported cases have been associated with systemic lupus erythematosus and there have been suggestions that Kikuchi's disease could represent a mild form of lupus but without definite evidence. We describe an unusual case of histiocytic necrotising lymphadenitis in an Asian woman who had recurrent episodes for five years before a diagnosis was made.

摘要

菊池-藤本病,又称组织细胞坏死性淋巴结炎,是一种病因不明的自限性疾病,其特征为淋巴结病、发热和中性粒细胞减少。一些报告的病例与系统性红斑狼疮有关,有人认为菊池病可能是狼疮的一种轻度形式,但尚无确凿证据。我们描述了一名亚洲女性的罕见组织细胞坏死性淋巴结炎病例,该患者在确诊前反复发病五年。

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