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头皮部伴淋巴样聚集的罕见血管肿瘤:血管淋巴样增生的一种变异型?

Unusual vascular tumour of the scalp in association with lymphoid aggregates: a variant of angiolymphoid hyperplasia?

作者信息

Dawson J, Mauduit G, Kanitakis J, Euvrard S, Thivolet J

出版信息

J Cutan Pathol. 1984 Dec;11(6):506-12. doi: 10.1111/j.1600-0560.1984.tb00411.x.

Abstract

A 51-year-old mason presented with a large tumour on his scalp which had developed over the previous 2 years. Histological examination showed the presence of large vessels with muscular coats some of which appeared to be venules and others arterioles. They had markedly swollen cuboidal endothelial cells and a surrounding mononuclear cell infiltrate which in areas formed lymphoid follicles some of which had germinal centers. There was no evidence of tissue or blood eosinophilia. The unusual clinical and histological features of this case are emphasized and the nosology of this rare condition is discussed.

摘要

一名51岁的泥瓦匠因头皮上出现一个在过去两年中逐渐增大的大肿瘤前来就诊。组织学检查显示存在有肌层的大血管,其中一些似乎是小静脉,另一些是小动脉。它们有明显肿胀的立方状内皮细胞以及周围的单核细胞浸润,在某些区域形成了淋巴滤泡,其中一些有生发中心。没有组织或血液嗜酸性粒细胞增多的证据。强调了该病例不寻常的临床和组织学特征,并讨论了这种罕见疾病的分类学。

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Angiolymphoid hyperplasia with eosinophilia simulating lymphadenopathy.
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