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酷似斯图尔特-特里夫斯综合征的马松血管内乳头状内皮增生:1例报告

Masson's intravascular papillary endothelial hyperplasia mimicking Stewart-Treves syndrome: report of a case.

作者信息

Romaní J, Puig L, Costa I, de Moragas J M

机构信息

Department of Dermatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Cutis. 1997 Mar;59(3):148-50.

PMID:9071555
Abstract

Masson's intravascular papillary endothelial hyperplasia, also called Masson's pseudoangiosarcoma, represents a benign vascular proliferation, presently considered as a peculiar histopathologic reaction pattern of the endothelium to diverse stimuli. Differentiation from angiosarcoma represents the main diagnostic concern. We report a case of Masson's intravascular papillary endothelial hyperplasia presenting in a 55-year-old woman with ipsilateral lymphedema secondary to surgery and radiation therapy for breast carcinoma. The diagnosis was intravascular papillary endothelial hyperplasia. This is the first description of Masson's pseudoangiosarcoma in this clinical context, to our knowledge. We believe it represents a peculiar morphologic pattern of endothelium proliferation secondary to venous stasis and thrombosis due to lymphedema.

摘要

马松氏血管内乳头状内皮细胞增生症,也称为马松氏假血管肉瘤,是一种良性血管增殖,目前被认为是内皮细胞对多种刺激的一种特殊组织病理学反应模式。与血管肉瘤的鉴别是主要的诊断关注点。我们报告一例马松氏血管内乳头状内皮细胞增生症,发生在一名55岁女性身上,该患者因乳腺癌手术和放疗后继发同侧淋巴水肿。诊断为血管内乳头状内皮细胞增生症。据我们所知,这是首次在这种临床背景下描述马松氏假血管肉瘤。我们认为它代表了由于淋巴水肿导致静脉淤滞和血栓形成后内皮细胞增殖的一种特殊形态模式。

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