Adrenocortical carcinoma: state of the art
Keywords:
Cushing síndrome, neoplasm metastasis, adrenal cortex neoplasmsAbstract
A 22 year-old woman presented with a 9-month history of a left breast tumor and a left adrenal mass in the context of a Cushing's syndrome. Her laboratory studies demonstrated high urinary cortisol excretion, abnormally elevated serum testosterone values, and suppressed ACTH. An abdominal CT scan revealed a mass in the left adrenal gland suggestive of adrenocortical cancer with distant metastasis to the liver and the lungs. Herein, we review and discuss the diagnosis and the therapeutic options for this rare and aggressive neoplasia.
Author Biographies
Nydia Elvira Pabón, Universidad Nacional de Colombia
Grupo Endocrinología; Universidad Nacional de Colombia, Bogotá, D.C., Colombia.
Constanza Gómez, Instituto Nacional de Cancerología
Grupo Patología Oncológica, Instituto Nacional de Cancerología E.S.E., Bogotá, D.C., Colombia.
Gloria Garavito, Instituto Nacional de Cancerología
Grupo Endocrinología Oncológica, Instituto Nacional de Cancerología E.S.E., Bogotá, D.C., Colombia
Camilo Jiménez, Instituto Nacional de Cancerología
Grupo Endocrinología Oncológica, Instituto Nacional de Cancerología E.S.E., Bogotá, D.C., Colombia
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