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孤立性促肾上腺皮质激素缺乏症伴多腺体功能衰竭。

Isolated adrenocorticotropin deficiency associated with polyglandular failure.

作者信息

Kojima I, Nejima I, Ogata E

出版信息

J Clin Endocrinol Metab. 1982 Jan;54(1):182-6. doi: 10.1210/jcem-54-1-182.

Abstract

A female patient presented with isolated ACTH deficiency and diabetes mellitus. During the course of a year's replacement with hydrocortisone, goiter developed, which, on biopsy, was diagnosed as typical Hashimoto's thyroiditis. Four years later, she experienced tetany, and the diagnosis of idiopathic hypoparathyroidism was made. Immunological studies revealed the presence of antithyroid antibodies in the serum and cell-mediated immunity to the thyroid and parathyroid. These data strongly suggest that the autoimmune process is involved in the genesis of some, though not all, forms of isolated ACTH deficiency.

摘要

一名女性患者出现孤立性促肾上腺皮质激素(ACTH)缺乏和糖尿病。在使用氢化可的松替代治疗的一年过程中,出现了甲状腺肿,经活检诊断为典型的桥本甲状腺炎。四年后,她发生了手足搐搦,诊断为特发性甲状旁腺功能减退症。免疫学研究显示血清中存在抗甲状腺抗体以及对甲状腺和甲状旁腺的细胞介导免疫。这些数据强烈提示自身免疫过程参与了部分(尽管不是全部)孤立性ACTH缺乏症的发病机制。

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