皮肤血管肉瘤的特点

Sinval Soares Cruvinel, Victor Parreira Bizinoto, Nádia Cristine Nunes Côrtes, Alexandre Macedo, D. Pereira, Antônio Ricardo Duarte
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引用次数: 0

摘要

皮肤血管肉瘤是一种罕见的软组织肉瘤,预后较差,发病率约为2.0%。这种实体表现为瘀伤,紫色结节和斑块,弥漫性出血性病变伴浸润性生长。我们在此报告一例80岁的白人男性,他在右耳的上三分之一出现结节状,坚硬和黑色病变超过1年。皮肤血管肉瘤的治疗是多学科的,包括单纯手术或早期病变联合放疗,弥散性病变联合化疗。皮肤肉瘤是罕见的,其适当的治疗和随访是至关重要的。■文摘
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peculiarities of cutaneous angiosarcoma
Cutaneous angiosarcoma is a rare soft tissue sarcoma with a poor prognosis and an incidence of approximately 2.0%. This entity manifests as bruises, violaceous nodules and plaques, and diffuse hemorrhagic lesions with infiltrative growth. Here we report a case of an 80-year-old Caucasian man who presented with a nodular, hard, and dark lesion present in the upper third of the right ear for more than 1 year. The treatment of cutaneous angiosarcoma is multidisciplinary, including surgery alone or combined with radiotherapy for early lesions and chemotherapy for disseminated lesions. Cutaneous sarcomas are rare, and their appropriate treatment and follow-up are critical. ■ ABSTRACT
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