Yilmaz M, Mamanov M A, Rashidov R, Ibrahimov M, Kyscu A, Karaman E
Vestn Otorinolaringol. 2012(1):65-6.
Kikuchi-Fujimoto's disease is a form of histocytic necrotizing lymphadenitis that largely affects women of Asian descent. The cause of this pathology remains to be elucidated although it is supposed that it has immunological and infectious nature. Clinically, Kikuchi-Fujimoto's disease manifests itself as unilateral lymphadenoapthy accompanied by febrile state and other non-specific symptoms. The diagnosis is based on the results of puncture (in the first place, excision) biopsy. No effective treatment of histocytic necrotizing lymphadenitis has thus far been proposed. Spontaneous regression of lymphadenopathy may occur within 1-6 months after the onset. A clinical observation of a 36 year-old patient presenting with a confirmed form of Kikuchi-Fujimoto's disease is presented.
菊池-藤本病是组织细胞坏死性淋巴结炎的一种形式,主要影响亚洲血统的女性。尽管推测其具有免疫和感染性质,但这种病理状况的病因仍有待阐明。临床上,菊池-藤本病表现为单侧淋巴结肿大,并伴有发热状态和其他非特异性症状。诊断基于穿刺(首先是切除)活检的结果。迄今为止,尚未提出对组织细胞坏死性淋巴结炎的有效治疗方法。淋巴结病可能在发病后1至6个月内自发消退。本文介绍了一名36岁确诊为菊池-藤本病患者的临床观察情况。