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菊池-藤本病:病例报告

Kikuchi-Fujimoto disease: case report.

作者信息

Kołodziej-Kłek Aneta, Orłowska-Florek Renata, Gałazka Krystyna, Grzywa Marek

机构信息

Department of Internal Diseases, Nephrology and Endocrinology, Regional Hospital No. 2, Rzeszów, Poland.

出版信息

Pol Arch Med Wewn. 2009 Dec;119(12):826-9.

PMID:20010470
Abstract

We present the case of a 27-year-old woman with local cervical lymphadenopathy without other symptoms. Due to a gradual progression of lesions, a biopsy was performed, and a specimen excised from an enlarged lymph node was subjected to histological examination. Kikuchi-Fujimoto disease (KFD), that is histiocytic necrotizing lymhadenitis, was diagnosed. Lymphadenopathy resolved without medical treatment over 6 months. KFD should be considered in the differential diagnosis of lymphadenopathy, even though this disease rarely occurs in Poland.

摘要

我们报告了一例27岁女性病例,该患者有局部颈部淋巴结病,但无其他症状。由于病变逐渐进展,遂进行了活检,从一个肿大的淋巴结切除的标本进行了组织学检查。诊断为菊池-藤本病(KFD),即组织细胞坏死性淋巴结炎。淋巴结病在6个月内未经治疗自行消退。尽管这种疾病在波兰很少见,但在淋巴结病的鉴别诊断中应考虑KFD。

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引用本文的文献

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A white man with Kikuchi-Fujimoto disease mimicking lymphoma, preceded by frequent episodes of tonsillitis: a case report.一名白人男性患类淋巴瘤性菊池-藤本病,之前有频繁的扁桃体炎发作:病例报告。
J Med Case Rep. 2017 Feb 12;11(1):39. doi: 10.1186/s13256-017-1208-4.