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[淋巴结朗格汉斯细胞组织细胞增多症]

[Langerhans cell histiocytosis of lymph node].

作者信息

Rovira E, Michavila J, Ferrando J, Belda A, Gonzalvo F, Redón J

机构信息

Servicio de Medicina Interna, Hospital de Sagunto, Universidad de Valencia.

出版信息

An Med Interna. 1996 Dec;13(12):589-91.

PMID:9063934
Abstract

Langerhans cell Histiocytosis or Histiocytosis X encompasses the syndromes of Letterer-Siwe disease, Hand-Schuller-Christian disease and eosinophilic granuloma. The localized disease usually consisted of isolated bone involvement as osteolytic areas. The isolated lymph node disease is uncommon. A case study of eosinophilic granuloma of lymph node in a 27 years-old woman who underwent several recurrences as lymphadenitis is presented. This case is presented in light of the cytologic, histologic and immunohistochemical findings of node-based eosinophilic granuloma and the favorable prognosis of this localized form treated with steroids.

摘要

朗格汉斯细胞组织细胞增多症或组织细胞增多症X包括勒-雪病、汉-许-克病和嗜酸性肉芽肿综合征。局限性疾病通常表现为孤立的骨受累,呈溶骨区。孤立的淋巴结疾病并不常见。本文介绍了一例27岁女性淋巴结嗜酸性肉芽肿的病例研究,该患者曾多次复发,表现为淋巴结炎。结合基于淋巴结的嗜酸性肉芽肿的细胞学、组织学和免疫组化结果以及用类固醇治疗这种局限性形式的良好预后,对该病例进行了介绍。

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