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表现为巨大侧腹肿块的良性淋巴管内皮瘤。

Benign lymphangioendothelioma presenting as a giant flank mass.

作者信息

Schnebelen Alicia M, Page James, Gardner Jerad M, Shalin Sara C

机构信息

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Arkansas Skin Cancer Center, Little Rock, AR, USA.

出版信息

J Cutan Pathol. 2015 Mar;42(3):217-221. doi: 10.1111/cup.12453. Epub 2014 Dec 23.

Abstract

Benign lymphangioendothelioma is a rare lesion of controversial etiology and a histopathologic mimic of Kaposi sarcoma and so-called 'well-differentiated' angiosarcoma. Its most typical clinical presentation is as a slowly expanding, erythematous patch or plaque; it rarely presents as a large mass. We report the second case of a giant benign lymphangioendothelioma, which arose as a serpiginous mass involving most of the flank of an elderly male with no prior radiation exposure and with a remote history of herpes zoster infection. A biopsy revealed numerous anastomosing vascular channels extending from the superficial dermis to the subcutis that were dilated to progressively slit-like in architecture. The endothelial cells lacked cytologic atypia, hobnailing, or significant mitotic activity, and human herpesvirus-8 expression was absent. Positivity for podoplanin (D2-40) was observed in the endothelial cells, supporting a lymphatic phenotype. Furthermore, the lesional cells lacked immunohistochemical expression of Wilms tumor 1, providing further support of a malformative - rather than neoplastic - pathogenesis.

摘要

良性淋巴管内皮瘤是一种病因存在争议的罕见病变,镜下表现易与卡波西肉瘤及所谓“高分化”血管肉瘤相混淆。其最典型的临床表现为缓慢扩大的红斑或斑块;很少表现为大肿块。我们报告了第二例巨大良性淋巴管内皮瘤病例,该肿瘤表现为匐行性肿块,累及一名老年男性大部分侧腹,该患者既往无放疗史,有带状疱疹感染史。活检显示大量吻合的血管通道从浅表真皮延伸至皮下,这些血管通道呈扩张状,逐渐呈裂隙状结构。内皮细胞缺乏细胞学异型性、鞋钉样表现或显著的有丝分裂活性,且无人类疱疹病毒8型表达。在内皮细胞中观察到足板蛋白(D2-40)阳性,支持淋巴管表型。此外,病变细胞缺乏Wilms瘤1的免疫组化表达,进一步支持了其发育异常而非肿瘤性的发病机制。

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