Hemangioendotelioma epitelioide pulmonar. Reporte de un caso.
Palabras clave:
Epitheliod Haemangioendothelioma, Lung Neoplasms, Weibel-Palade BodiesResumen
Epithelioid hemangioendothelioma is a multifocal tumor that rarely metastasizes. It is difficult to diagnose, most often it is an incidental finding in young asymptomatic women. The radiologic pattern is heterogeneous. Histologic confirmation of Weibel-Palade bodies or immunohistochemistry based on specific tumor markers such as factor VIII and CD34 are the most important finding to confirm the diagnosis. We report a 21 years old woman Presenting with cough and dyspnea. A chest X ray was suggestive of tuberculosis. Sputum smears were negative for acid fat bacilli and the tuberculin test was negative. A chest CAT scan showed multiple nodular lesions. A surgical biopsy of the lesions confirmed the presence of a hemangioendothelioma. The patient was initially treated with prednisone and azathioprine without response. Thereafter, the patient is without treatment and without evidence of disease progression.Descargas
Publicado
2017-05-19
Cómo citar
Quiroz, M., Undurraga, Álvaro, Moya, R., Fernández, C., Bezares, K., & Linacre, V. (2017). Hemangioendotelioma epitelioide pulmonar. Reporte de un caso. Revista Médica De Chile, 145(5). Recuperado a partir de https://revistamedicadechile.cl/index.php/rmedica/article/view/5573
Número
Sección
Reporte de Caso Clínico