复发性菊池藤本氏病伴有无菌性脑膜炎和家族遗传:罕见病例

Nalika Lakmali, Ranga Chamara, Tiron Chathuranga, Meththananda Herath
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引用次数: 0

摘要

伴有神经系统表现的复发性菊池藤本氏病(KFD)是一种罕见病。它通常表现为发热和颈淋巴结病变。诊断依据是临床表现和淋巴结活检的典型组织学结果。大多数情况下,KFD 是自限性的。我们报告了一例复发性 KFD 病例,患者是一名 28 岁的男性,表现为无菌性脑膜炎,有 KFD 家族史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent Kikuchi Fujimoto Disease with Aseptic Meningitis and Familial Occurrence: A Rare Presentation
Recurrent Kikuchi Fujimoto Disease (KFD) with neurological manifestations is a rare entity. It usually presents with fever and cervical lymphadenopathy. Diagnosis is based on clinical grounds and typical histological findings of lymph node biopsy. Mostly KFD is self-limiting. Treatment with non-steroidal anti-inflammatory drugs or steroids may be needed in severe recurrent disease.We report a case of recurrent KFD in a 28-year-old male presenting with aseptic meningitis who has a family history of KFD.
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