ResumenEl hemangioendotelioma epitelial es una neoplasia poco frecuente, y tiene su origen en el endotelio vascular. Puede crecer en varios órganos y tejidos. No hay ningún esquema terapéutico aprobado y el pronóstico es impredecible. Se presenta el caso de un paciente masculino de 54 años de edad, con el diagnóstico de hemangioendotelioma epitelioide pulmonar, con imagen atípica y la presentación clínica y la participación de múltiples órganos en el momento del diagnóstico. El paciente no comenzó la quimioterapia y murió dos meses después del diagnóstico histológico. Debido a la rareza de esta neoplasia y la inexistencia de régimen terapéu-tico aprobado, al reportar este caso, tenemos la intención de contribuir a los estudios clínicos futuros. Palabras clave: Pulmón. Hemangioendotelioma epitelioide. Inhibidores de la angiogénesis
AbstractEpithelioid Hemangioendothelioma is a rare neoplasia, and has its origin in the vascular endothelium. It may grow in several organs and tissues. There is not any approved therapeutic scheme and the prognosis is unpredictable. It is reported the case of a 54-year-old male patient, with the diagnosis of pulmonary epithelioid hemangioendothelioma, with atypical imaging and clinical presentation and multiple organ involvement at the time of the diagnosis. The patient did not start chemotherapy and died two months after the histological diagnosis. Due to the rarity of this neoplasia and the inexistence of approved therapeutic scheme, by reporting this case we intend to contribute to future clinical studies.
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