Kikuchi Fujimoto disease

Rajan J. Unadkat , Shaila R. Khubchandani , Ashish S. Gurjar
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引用次数: 1

Abstract

Kikuchi Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis is an uncommon, idiopathic, generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. Fujimoto and colleagues described Kikuchi's disease in the same year. The cause of Kikuchi-Fujimoto's disease is unknown. Some kind of viral or post viral aetiology has been proposed. There have also been reports of a possible link between KFD and Systemic Lupus erythematosus (SLE).

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Kikuchi Fujimoto病(KFD),也被称为组织细胞坏死性淋巴结炎,是一种罕见的,特发性的,通常自限性的淋巴结炎原因。菊地最早于1972年在日本描述了这种疾病。藤本和他的同事在同一年描述了菊池的疾病。菊池-藤本氏病的病因尚不清楚。有人提出了某种病毒或后病毒病原学。也有报道称KFD与系统性红斑狼疮(SLE)之间可能存在联系。
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