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Artigo em Inglês | IMSEAR | ID: sea-125119

RESUMO

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.


Assuntos
Idoso , Biópsia por Agulha Fina , Cistadenocarcinoma/diagnóstico , Evolução Fatal , Feminino , Ducto Hepático Comum/patologia , Humanos , Testes de Função Hepática , Neoplasias Hepáticas/diagnóstico
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