Fernandez-Fernandez F, Halperin I, Manzanares J M, Flores L, Lomeña F, Vilardell E
Endocrinology and Nutrition Unit, Hospital Clinic, Barcelona, Spain.
J Endocrinol Invest. 1997 Jun;20(6):327-30. doi: 10.1007/BF03350311.
Bronchial carcinoid tumor is the most frequent occult source of ectopic ACTH-dependent Cushing's syndrome, but its initial localization may be very difficult, as well as its postoperative follow-up. We here present the case of a 21-year-old man with Cushing's syndrome and biochemical findings suggesting an ectopic source of ACTH (lack of inhibition of cortisol after overnight 8-mg dexamethasone suppression test, and lack of response to h-CRH challenge). Chest CT-scan showed a node adjacent to the left lung hilium whose nature was confirmed by uptake of 111Indium-DTPA labelled octreotide scintigraphy. Surgical resection of the tumor consisted in an upper lobectomy of the left lung. Microscopic examination identified a typical carcinoid tumor. After surgery pituitary-adrenal function normalized and a second scintigraphy offered additional data on the absence of tumor remnants.
支气管类癌瘤是异位促肾上腺皮质激素(ACTH)依赖性库欣综合征最常见的隐匿性病因,但其初始定位以及术后随访可能都非常困难。我们在此介绍一名21岁患有库欣综合征的男性病例,其生化检查结果提示ACTH存在异位来源(过夜8毫克地塞米松抑制试验后皮质醇未被抑制,且对人促肾上腺皮质激素释放激素[h-CRH]激发试验无反应)。胸部CT扫描显示左肺门旁有一个结节,111铟-二乙三胺五乙酸(111Indium-DTPA)标记的奥曲肽闪烁扫描摄取证实了其性质。肿瘤的手术切除包括左肺上叶切除术。显微镜检查确定为典型类癌瘤。术后垂体-肾上腺功能恢复正常,第二次闪烁扫描提供了关于无肿瘤残留的更多数据。