A Case of Adrenocortical Carcinoma Secreting Cortisol, Androgen and Aldosterone
Endocrinology and Metabolism
;
: 239-242, 2011.
Artigo
em Coreano
| WPRIM
| ID: wpr-108686
ABSTRACT
Primary adrenocortical carcinoma is a rare tumor, and is characterized by a peri-tumor mass effect and hormone excess signs. Adrenocortical carcinoma most commonly secretes cortisol, but tumors that secrete other adrenal hormones (aldosterone, androgen) are rare. Herein, we report the case of a 70-year-old woman with cortisol, androgen, and aldosterone-secreting adrenal carcinoma. The patient complained of generalized weakness, moon face, and central obesity. On laboratory examination, hypokalemia and metabolic alkalosis was detected. On the hormone test, cortisol, DHEA-S, and aldosterone were all increased. Abdominal CT showed a large right adrenal mass. She underwent right adrenalectomy and the histology revealed the presence of an adrenocortical carcinoma. After adrenalectomy, the patient was treated with hydrocortisone and mitotane.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Hidrocortisona
/
Carcinoma Adrenocortical
/
Adrenalectomia
/
Síndrome de Cushing
/
Aldosterona
/
Alcalose
/
Obesidade Abdominal
/
Hipopotassemia
/
Mitotano
Limite:
Idoso
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Endocrinology and Metabolism
Ano de publicação:
2011
Tipo de documento:
Artigo
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