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[嗜酸性粒细胞增多性血管淋巴样增生(木村病)]

[Angiolymphoid hyperplasia with eosinophilia (Kimura disease)].

作者信息

Kalamkarian A A, Vavilov A M, Persina I S

出版信息

Arkh Patol. 1987;49(3):76-8.

PMID:3593012
Abstract

Angiolymphoid hyperplasia with eosinophilia (ALHE) is characterized by the appearance of tumour-like nodes on skin and subcutaneous fat. Vascular proliferation with inflammatory infiltration consisting of lymphocytes and eosinophiles, as well as structures of lymphoid follicle type were revealed microscopically. A description is given of a patient, 34 yr. old, with typical clinical and morphological manifestations of ALHE. Basing on the literature and on the own experience the authors suggest that ALHE and Kimura disease are variants of one nosologic form.

摘要

嗜酸性粒细胞增多性血管淋巴样增生(ALHE)的特征是在皮肤和皮下脂肪出现肿瘤样结节。显微镜下可见血管增生伴淋巴细胞和嗜酸性粒细胞组成的炎症浸润以及淋巴滤泡样结构。本文描述了一名34岁患有典型ALHE临床和形态学表现的患者。基于文献和自身经验,作者认为ALHE和木村病是同一种疾病形式的变体。

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