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Hepatoid Adenocarcinoma of the Duodenum: An Unusual Location.
Ogbonna, Onyekachi Henry; Sakruti, Susmita; Sulieman, Maha; Ali, Ahmed; Shokrani, Babak; Oneal, Patricia.
Afiliação
  • Ogbonna OH; Division of Hematology and Oncology, Department of Internal Medicine, Howard University Hospital, Washington, D.C., USA.
  • Sakruti S; Division of Hematology and Oncology, Department of Internal Medicine, Howard University Hospital, Washington, D.C., USA.
  • Sulieman M; Departments of Internal Medicine, Howard University Hospital, Washington, D.C., USA.
  • Ali A; Division of Hematology and Oncology, Department of Internal Medicine, Howard University Hospital, Washington, D.C., USA.
  • Shokrani B; Pathology, Howard University Hospital, Washington, D.C., USA.
  • Oneal P; Division of Hematology and Oncology, Department of Internal Medicine, Howard University Hospital, Washington, D.C., USA.
Case Rep Oncol ; 9(1): 182-7, 2016.
Article em En | MEDLINE | ID: mdl-27064217
Hepatoid adenocarcinoma (HAC) is a rare extrahepatic tumor distinguished by having both hepatoid and adenomatous features, which can make the diagnosis challenging. Although it mostly originates in the stomach, several other sites of origin have been reported. We report a case of HAC originating in the duodenum, a very unusual location. We also discuss an approach to the diagnosis of HAC using morphological and immunohistochemical features, and explore possible therapeutic options.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article