A Case of Bilateral Adrenal Myelolipomas with Congenital Adrenal Hyperplasia / 대한내과학회지
Korean Journal of Medicine
;
: 340-345, 2015.
Artículo
en Coreano
| WPRIM
| ID: wpr-216643
ABSTRACT
Adrenal myelolipoma (AML) is a rare, usually benign, and nonfunctioning tumor. About 7-15% of adrenal incidentalomas are AMLs, composed of normal hematopoietic elements and mature adipose tissue. AML is usually unilateral and < 4 cm. It is often discovered incidentally on abdominal computed tomography or magnetic resonance imaging. It is related to a chronic increase in adrenocorticotropic hormone, such as that observed in patients with congenital adrenal hyperplasia, Cushing disease, Conn's syndrome, and pheochromocytoma. Here, we report a 28-year-old man diagnosed with non-salt-losing congenital adrenal hyperplasia with huge bilateral AMLs and a literature review.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Feocromocitoma
/
Imagen por Resonancia Magnética
/
Tejido Adiposo
/
Mielolipoma
/
Hiperplasia Suprarrenal Congénita
/
Hormona Adrenocorticotrópica
/
Hipersecreción de la Hormona Adrenocorticotrópica Pituitaria (HACT)
/
Hiperaldosteronismo
Límite:
Adulto
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Medicine
Año:
2015
Tipo del documento:
Artículo
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