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KMID : 0882420150890030340
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Korean Journal of Medicine
2015 Volume.89 No. 3 p.340 ~ p.345
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A Case of Bilateral Adrenal Myelolipomas with Congenital Adrenal Hyperplasia
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Lee Jung-Hoon
Kim Ji-Yoon
Kwon Jae-Wan
Lee Joon-Kee
Jeon Eon-Ju
Jung Eui-Dal
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Abstract
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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.
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KEYWORD
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Adrenal, Myelolipoma, Adrenal hyperplasia, Congenital
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