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[组织细胞性坏死性淋巴结炎(菊池病):一例报告]

[Histiocytic necrotizing lymphadenitis (Kikuchi disease): a case report].

作者信息

Rozwens A, Molska M, Karlińska M, Klicki G

机构信息

Oddział Chorób Wewnetrznych i Kardiologii SP ZOZ w Leborku.

出版信息

Pol Merkur Lekarski. 2001 Sep;11(63):259-60.

Abstract

Histicytic necrotizing lymphadenitis (Kikuchi disease) is a benign, self-limited disorder occurring in young adults, that is sometimes confused with malignant lymphoma. A definitive etiology has been not identified. Kikuchi's disease is characterized by collections of histiocytes and lymphocytes surrounding areas of necrosis in lymph nodes, containing fragments of karyorrhectic nuclear debris. There has been a report of a case of Kikuchi disease. We suggest that Kikuchi disease be considered as one of the differential diagnoses in young patients presenting with cervical lymphadenopathy and fever of unknown origin.

摘要

组织细胞坏死性淋巴结炎(菊池病)是一种发生于年轻人的良性自限性疾病,有时会与恶性淋巴瘤相混淆。确切病因尚未明确。菊池病的特征是淋巴结内坏死区域周围有组织细胞和淋巴细胞聚集,其中含有核碎裂的核碎片。曾有一例菊池病的报道。我们建议,对于出现颈部淋巴结病和不明原因发热的年轻患者,应将菊池病列为鉴别诊断之一。

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