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Artículo en Inglés | IMSEAR | ID: sea-125119

RESUMEN

Biliary cystadenocarcinoma (BCAC) is a rare cystic tumour of the liver; with its benign counterpart, it accounts for <5% of non-parasitic hepatic cysts. Preoperative diagnosis of BCAC is difficult; complete surgical excision is recommended to prevent recurrence or metastasis. We present the case of a 67-year-female with centrally located BCAC involving the right hepatic duct and distorting the hepatic hilum. This report highlights the difficulties in diagnosis, surgical resection, subsequent biliary reconstruction and its outcome.


Asunto(s)
Anciano , Biopsia con Aguja Fina , Cistadenocarcinoma/diagnóstico , Resultado Fatal , Femenino , Conducto Hepático Común/patología , Humanos , Pruebas de Función Hepática , Neoplasias Hepáticas/diagnóstico
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