Revista: | Anais brasileiros de dermatologia |
Base de datos: | PERIÓDICA |
Número de sistema: | 000408856 |
ISSN: | 0365-0596 |
Autores: | Cabral, Aline Neves Freitas1 Rocha, Rafael Henrique1 Amaral, Ana Cristina Vervloet do1 Medeiros, Karina Bittencourt2 Nogueira, Paulo Sergio Emerich1 Diniz, Lucia Martins2 |
Instituciones: | 1Universidade Federal do Espirito Santo, Hospital Universitario Cassiano Antonio Moraes, Vitoria, Espirito Santo. Brasil 2Universidade Federal do Espirito Santo, Faculdade de Medicina, Vitoria, Espirito Santo. Brasil |
Año: | 2017 |
Periodo: | Mar-Abr |
Volumen: | 92 |
Número: | 2 |
Paginación: | 238-241 |
País: | Brasil |
Idioma: | Inglés |
Tipo de documento: | Artículo |
Enfoque: | Caso clínico, descriptivo |
Resumen en inglés | Angiosarcoma is a rare and aggressive tumor with high rates of metastasis and relapse. It shows a particular predilection for the skin and superficial soft tissues. We report three distinct and typical cases of angiosarcoma that were diagnosed in a single dermatology clinic over the course of less than a year: i) Angiosarcoma in lower limb affected by chronic lymphedema, featuring Stewart-Treves syndrome; ii) a case of the most common type of angiosarcoma loated in the scalp and face of elderly man and; iii) a skin Angiosarcoma in previously irradiated breast. All lesions presented characteristic histopathological findings: irregular vascular proliferation that dissects the collagen bundles with atypical endothelial nuclei projection toward the lumen |
Disciplinas: | Medicina |
Palabras clave: | Dermatología, Diagnóstico, Oncología, Angiosarcoma, Hemangiosarcoma, Linfangiosarcoma, Linfedema, Histopatología |
Keyword: | Medicine, Dermatology, Diagnosis, Oncology, Angiosarcoma, Hemangiosarcoma, Lymphangiosarcoma, Lymphedema, Histopathology |
Texto completo: | Texto completo (Ver HTML) |