Hemangioendotelioma epitelioide cutáneo extenso multifocal agresivo. Informe de un caso

Mario Murguía-Pérez , Sandra Zynzya Enríquez-Brena , Saulo Mendoza-Ramírez , Rafael Fosado-Ramos , Yunuén Ibiza García-Mendoza , Lázaro Ramírez-Balderrama , Blanca Elena Verazaluce-Rodríguez , Martha Alicia Hernández-González , Blanca Olivia Murillo-Ortiz
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引用次数: 0

Abstract

Epithelioid haemangioendothelioma is a rare vascular tumor, first described in 1975 by Dail and Liebow as a bronchioloalveolar carcinoma. Although it usually behaves like a low-grade neoplasm, cases have been reported in which the tumor shows a high grade of malignancy, spreading rapidly throughout the body. We present the case of a 41-year-old man with dermatosis in the left thigh with rapid extension to the abdomen; the initial differential diagnoses were metastatic carcinoma versus lymphoma.

When the histopathology was re-examined, a diagnosis of skin epithelioid hemangioendothelioma was confirmed and treatment with radiotherapy was initiated.

This tumour rarely affects the skin; there are only a few previously reported cases.

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侵袭性多灶性广泛皮肤上皮样血管内皮瘤。报告一宗个案
上皮样血管内皮瘤是一种罕见的血管肿瘤,于1975年由Dail和Liebow首次描述为细支气管肺泡癌。虽然它通常表现为低级别肿瘤,但也有报道称肿瘤表现为高级别恶性肿瘤,迅速传遍全身。我们提出的情况下,41岁的男子皮肤病在左大腿迅速扩展到腹部;最初的鉴别诊断是转移性癌和淋巴瘤。复查组织病理学,确诊为皮肤上皮样血管内皮瘤,并开始放疗治疗。这种肿瘤很少影响皮肤;以前报告的病例很少。
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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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