Suppr超能文献

[颈部淋巴结病的罕见病例——菊池-藤本病]

[A rare case of cervical lymphadenopathy--Kikuchi-Fujimoto's disease].

作者信息

Yilmaz M, Mamanov M A, Rashidov R, Ibrahimov M, Kyscu A, Karaman E

出版信息

Vestn Otorinolaringol. 2012(1):65-6.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验