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阴茎平滑肌肉瘤。超微结构研究(作者译)

[Penile leiomyosarcoma. Ultrastructural study (author's transl)].

作者信息

Armijo M, Herrera E, de Dulanto F, Naranjo R, Camacho F

出版信息

Ann Dermatol Venereol. 1978 Mar;105(3):267-74.

PMID:677694
Abstract

A case of leiomyosarcoma of the penis in a farmer aged 70 is described. The patient was treated by excision/biopsy, and six months later three little tumors recurred on the glans and prepuce. A wide local excision and direct suture was carried out. No troubles happened in the next eight months. The ultrastructural study confirmed the histogenesis showing: polymorphic cells, as well as clear and dark ones, reduction of intracytoplasmic myofilaments, anisocytosis and poikilokaryosis and wide infoldings of the nuclear membrane; very vascularized areas with confluent vesicles on the endothelial cells; and intersticial haemorrhages. This tumor is included among the superficial leiomyosarcomas of "low malignancy" of McKenzie Pratt et Ross, for which simple excision that avoid mutilations is suitable. Differential histologic diagnosis includes epithelioid sarcoma of Enzinger. Leiomyosarcoma of the penis is a very rare malinant tumor. Only 15 cases have been described in the literature. A further case is reported and the previous cases are reviewed.

摘要

本文描述了一名70岁农民阴茎平滑肌肉瘤的病例。患者接受了切除/活检治疗,6个月后龟头和包皮上复发了3个小肿瘤。进行了广泛的局部切除和直接缝合。接下来的8个月没有出现问题。超微结构研究证实了组织发生,表现为:多形性细胞,包括透明和深色细胞,胞浆内肌丝减少,细胞大小不均和异形核,核膜广泛内褶;血管丰富区域的内皮细胞有融合的小泡;以及间质出血。该肿瘤属于麦肯齐·普拉特和罗斯的“低恶性”浅表平滑肌肉瘤,适合进行避免致残的简单切除。组织学鉴别诊断包括恩津格上皮样肉瘤。阴茎平滑肌肉瘤是一种非常罕见的恶性肿瘤。文献中仅描述了15例。本文报告了另一例病例并对先前病例进行了回顾。

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