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嗜酸性粒细胞增多性血管淋巴样增生:一例病程极长的类似软组织肿瘤病变的报告。

Angiolymphoid hyperplasia with eosinophilia: report of a lesion mimicking soft tissue tumor of extremely long duration.

作者信息

Tóth E, Orosz Z, Rahóty P

机构信息

Department of Surgery, National Institute of Oncology, Budapest, Hungary.

出版信息

Pathol Res Pract. 2000;196(2):99-101. doi: 10.1016/S0344-0338(00)80040-0.

DOI:10.1016/S0344-0338(00)80040-0
PMID:10707366
Abstract

We present a large sized lesion of the right upper arm in which characteristics of the angiolymphoid hyperplasia with eosinophilia (ALHE) intermingled with those of Kimura's disease (KD). The laboratory findings, the prominent vascular proliferation and the features of endothelial cells were suggestive of ALHE. However, the long duration of the disease, the site of involvement, the abundant lymphoid component forming lymph follicles with germinal centers and the fibrosis are features of KD. In agreement with other reports, our case shows that clinicopathologically there is an overlap between ALHE and KD.

摘要

我们展示了一例右上臂的大尺寸病变,其中嗜酸性粒细胞增多性血管淋巴样增生(ALHE)的特征与木村病(KD)的特征相互交织。实验室检查结果、显著的血管增生以及内皮细胞特征提示为ALHE。然而,病程较长、受累部位、形成带有生发中心的淋巴滤泡的丰富淋巴成分以及纤维化是KD的特征。与其他报告一致,我们的病例表明,在临床病理学上,ALHE和KD之间存在重叠。

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