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선천성부신과다형성증 환자에게서 발생한 부신 골수지방종 1예
이정훈 ( Jung Hoon Lee ),김지윤 ( Ji Yoon Kim ),권재완 ( Jae Wan Kwon ),이준기 ( Joon Kee Lee ),전언주 ( Eon Ju Jeon ),정의달 ( Eui Dal Jung ) 대한내과학회 2015 대한내과학회지 Vol.89 No.3
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. (Korean J Med 2015;89:340-345)