Hoffman L, Martin F I, Buchanan M R, Butkus A, Whitworth J A
Aust N Z J Med. 1980 Dec;10(6):654-6. doi: 10.1111/j.1445-5994.1980.tb04248.x.
A 35-year-old man with Cushing's syndrome due to ectopic ACTH production is described. The six-week history and severe proximal myopathy were highly suggestive of a malignant tumour, but a solitary phaeochromocytoma of the left adrenal gland was the source of ACTH production. The surgical outcome was successful and three months post-operatively the hypothalamic-pituitary-adrenal axis was normal. At 12 months follow-up he remains well with complete regression of the features of Cushing's syndrome.
本文描述了一名因异位促肾上腺皮质激素(ACTH)分泌导致库欣综合征的35岁男性患者。六周的病史及严重的近端肌病强烈提示为恶性肿瘤,但左侧肾上腺的孤立性嗜铬细胞瘤才是ACTH的分泌来源。手术结果成功,术后三个月下丘脑-垂体-肾上腺轴恢复正常。在12个月的随访中,他情况良好,库欣综合征的症状完全消退。