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淋巴管瘤样卡波西肉瘤:病因及文献综述

Lymphangioma-like Kaposi's sarcoma: etiology and literature review.

作者信息

Davis D A, Scott D M

机构信息

Departments of Dermatology and Pathology, University of Alabama at Birmingham, 35294-0009, USA.

出版信息

J Am Acad Dermatol. 2000 Jul;43(1 Pt 1):123-7. doi: 10.1067/mjd.2000.105564.

Abstract

Much confusion surrounds a rare and occasionally described variant of Kaposi's sarcoma (KS) known as lymphangioma-like or bullous KS. We describe the typical clinical and histologic features and elucidate the etiologic cell in lymphangioma-like KS. A computer-based review of the English-language literature was performed. Routine histologic and immunoperoxidase techniques were performed on formalin-fixed tissue. Immunoperoxidase staining for anti-CD31, anti-CD34, and anti-factor VIII-related antigen suggests that the etiologic cell of origin is the vascular endothelial cell. Lymphangioma-like KS has been described for more than a century and given various names. Dilated vascular spaces correlate with the clinically bullous lesions, which are veritable KS and not a secondary reaction to it.

摘要

一种罕见且偶尔被描述的卡波西肉瘤(KS)变体,即淋巴管瘤样或大疱性KS,存在诸多混淆之处。我们描述了其典型的临床和组织学特征,并阐明了淋巴管瘤样KS中的病因细胞。对英文文献进行了基于计算机的检索。对福尔马林固定的组织进行了常规组织学和免疫过氧化物酶技术检测。抗CD31、抗CD34和抗因子VIII相关抗原的免疫过氧化物酶染色表明,起源的病因细胞是血管内皮细胞。淋巴管瘤样KS已被描述了一个多世纪,并有各种名称。扩张的血管间隙与临床上的大疱性病变相关,这些病变是名副其实的KS,而非对其的继发反应。

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