Maschler I, Rosenmann E, Ehrenfeld E N
Clin Endocrinol (Oxf). 1979 May;10(5):493-7. doi: 10.1111/j.1365-2265.1979.tb02106.x.
A 26-year-old man with the Nelson's syndrome is described, in whom an abdominal tumour developed, accompanied by recurrent Cushing's syndrome 11 years after total adrenalectomy. Upon removal the tumour was a myelolipoma containing islands of adrenocortical-like elements. On incubation of the tumour with radioactive precursors, its capacity to produce cortisol in vitro was shown. The name adrenocortico-myelolipoma is suggested for this tumour.
本文描述了一名患有纳尔逊综合征的26岁男性,在其全肾上腺切除术后11年,出现了腹部肿瘤,并伴有复发性库欣综合征。切除的肿瘤为髓质脂肪瘤,含有肾上腺皮质样细胞岛。将肿瘤与放射性前体一起孵育后,显示其在体外具有产生皮质醇的能力。建议将此肿瘤命名为肾上腺皮质髓质脂肪瘤。