A Case of Adrenocortical Oncocytoma Misrecognized for Fibrolamellar Hepatocellular Carcinoma
Korean Journal of Hepato-Biliary-Pancreatic Surgery
;
: 184-188, 2009.
Artigo
em Coreano
| WPRIM
| ID: wpr-193886
ABSTRACT
Adrenocortical oncocytoma is a very rare disease which has been reported in 40 cases. A 27-years-old female patient was admitted for a suspicious hepatocellular mass on ultrasonogram. On CT scan, sono-guided needle biopsy and 18F-FDG PET scan, all results were unsatisfactory. During laparotomy, the mass was originated from Rt. adrenal gland and liver was pushed sideward by the mass. On pathology report, an adrenocortical oncocytoma was diagnosed. Adrenocortical oncocytoma has pathological characteristics comprised of oncocytes with granular, eosinophilic cytoplasm, and sufficient mitochondria in their cytoplasm. There were no established criteria for differential diagnose between benign and malignant adrenocortical oncocytoma. There are no sufficient data for the long-term outcome of adrenocortical oncocytoma in the medical literature. Thus we report a case of adrenocortical oncocytoma with review of the related literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Biópsia por Agulha
/
Glândulas Suprarrenais
/
Adenoma Oxífilo
/
Carcinoma Hepatocelular
/
Fluordesoxiglucose F18
/
Células Oxífilas
/
Citoplasma
/
Doenças Raras
/
Tomografia por Emissão de Pósitrons
/
Eosinófilos
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Hepato-Biliary-Pancreatic Surgery
Ano de publicação:
2009
Tipo de documento:
Artigo
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