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甲状腺髓样癌和嗜铬细胞瘤患者的肾上腺皮质功能。

Adrenal-cortical function in patients with medullary carcinoma of the thyroid and pheochromocytoma.

作者信息

Feldman J M, Wells S A

出版信息

Horm Metab Res. 1979 Oct;11(10):567-70. doi: 10.1055/s-0028-1092781.

Abstract

Medullary carcinoma of the thyroid (MCT) is reported to synthesize ACTH. This ACTH is believed to be responsible for the development of Cushing's syndrome in some patients with MCT. To determine the frequency of occurrence of adrenal cortical overactivity in patients with MCT, we measured plasma cortisol concentration and the urinary excretion of 17-hydroxycorticosteroids, 17-ketosteroids and urinary free cortisol in 22 patients with MCT and 7 patients with MCT plus pheochromocytomas. The patients with MCT and MCT plus pheochromocytoma had similar adrenal cortical function to age and sex matched normal subjects. We conclude that adrenal cortical function is usually normal in patients with MCT.

摘要

据报道,甲状腺髓样癌(MCT)可合成促肾上腺皮质激素(ACTH)。这种ACTH被认为是导致一些MCT患者发生库欣综合征的原因。为了确定MCT患者肾上腺皮质功能亢进的发生率,我们测量了22例MCT患者以及7例合并嗜铬细胞瘤的MCT患者的血浆皮质醇浓度、尿17-羟皮质类固醇、17-酮类固醇及尿游离皮质醇的排泄量。MCT患者以及合并嗜铬细胞瘤的MCT患者的肾上腺皮质功能与年龄和性别匹配的正常受试者相似。我们得出结论,MCT患者的肾上腺皮质功能通常是正常的。

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