Cutaneous Myopericytoma: A Report of 3 Cases and Review of the Literature

IF 1.6 Q3 DERMATOLOGY
Dermatopathology Pub Date : 2015-02-11 DOI:10.1159/000371875
P. Aung, L. Goldberg, M. Mahalingam, J. Bhawan
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引用次数: 20

Abstract

Cutaneous myopericytoma is a rarely reported mesenchymal neoplasm with a benign biologic behavior. It is seen more commonly in males and typically occurs in adults on the distal extremities. To the best of our knowledge, there are only 13 reports describing 45 cases of cutaneous myopericytoma in the literature. The 3 cases in this report expand the clinical presentation and reinforce the histopathologic features of cutaneous myopericytoma. While the clinical presentation in 2 cases (located on the scalp and heel) was in keeping with that reported previously of a slow-growing painless firm nodule, the third case, located on the dorsal wrist, presented as a scaly keratotic nodule. Histopathologic examination of all 3 cases revealed an unencapsulated dermal nodule with concentric perivascular arrangement of plump, spindle-shaped myoid cells admixed with thin-walled blood vessels. Immunohistochemical staining revealed the lesional cells to be actin- (3/3) and caldesmon- (2/3) positive and negative for other smooth muscle markers, compatible with perivascular myopericytic differentiation.
皮肤肌外皮细胞瘤3例报告并文献复习
摘要皮肤肌外皮细胞瘤是一种少见的良性间充质肿瘤。它更常见于男性,通常发生在成人远端肢体。据我们所知,文献中只有13篇报道描述了45例皮肤肌外皮细胞瘤。本报告的3例病例扩大了皮肤肌外皮细胞瘤的临床表现,强化了皮肤肌外皮细胞瘤的组织病理特征。2例(位于头皮和脚后跟)的临床表现与先前报道的生长缓慢的无痛性硬结节一致,第三例位于腕背,表现为鳞状角化性结节。3例患者的组织病理学检查均发现一未包封的真皮结节,其血管周围呈同心状排列,有饱满的纺锤状肌样细胞混杂薄壁血管。免疫组化染色显示病变细胞肌动蛋白-(3/3)和caldesmon-(2/3)阳性,其他平滑肌标志物阴性,与血管周围肌周细胞分化相符。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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