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J Cancer Res Ther ; 14(Supplement): S533-S535, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29970720

RESUMO

Primary pulmonary epithelioid angiosarcoma is an extremely rare malignancy. Herein, we report the case of an elderly Chinese patient with primary pulmonary epithelioid angiosarcoma. The 72-year-old man presented with a 1-month history of persistent hemoptysis and left chest pain and weight loss of 3 kg. A chest computed tomography (CT) scan revealed two masses (maximum size 3.0 cm × 2.0 cm and 0.8 cm × 0.5 cm) in right lower lobe. We performed a left thoracotomy for tumor resection. Pathological examination showed that there was a significant amount of hemorrhage, fibrinous exudates, degeneration, and necrosis. With immunohistochemical analysis, tumor cells had strong expression of CD34, FLI-1, vimentin. Morphological and immunohistochemical findings supported the diagnosis of epithelioid angiosarcoma.


Assuntos
Hemangiossarcoma/diagnóstico , Neoplasias Pulmonares/diagnóstico , Idoso , Biópsia , Terapia Combinada , Hemangiossarcoma/metabolismo , Hemangiossarcoma/terapia , Humanos , Imuno-Histoquímica , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/terapia , Masculino , Tomografia Computadorizada por Raios X , Resultado do Tratamento
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