Hashimoto K, Kurokawa H, Nishioka T, Takao T, Takeda K, Takamatsu K, Numata Y
Second Department of Internal Medicine, Kochi Medical School, Japan.
Endocr J. 1994 Dec;41(6):613-21. doi: 10.1507/endocrj.41.613.
Four cases of polyglandular endocrine disorders associated with pituitary hormone secretion failure are reported. Three of them had both insulin dependent diabetes mellitus (IDDM) and Hashimoto's disease. Each of these patients (cases 1-3) showed isolated deficiency of ACTH, TSH or gonadotropin, respectively. Another patient (case 4) had both Hashimoto's disease and isolated ACTH deficiency. Anti-pituitary antibody to AtT-20 cells was detected in case 1. Serum gamma-globulins from patients 1 and 4 attenuated corticotropin releasing hormone-induced ACTH release in monolayer cultured rat anterior pituitary cells. Gamma-globulins from patients 1 and 2 decreased baseline TSH release but stimulated baseline prolactin release in pituitary cell cultures. It is possible that pituitary hormone deficiency in these patients may be caused by autoimmune disorders.
本文报告了4例与垂体激素分泌衰竭相关的多腺体内分泌疾病。其中3例患有胰岛素依赖型糖尿病(IDDM)和桥本氏病。这些患者(病例1 - 3)分别表现为促肾上腺皮质激素(ACTH)、促甲状腺激素(TSH)或促性腺激素的单一缺乏。另一名患者(病例4)患有桥本氏病和单一ACTH缺乏。在病例1中检测到针对AtT - 20细胞的抗垂体抗体。患者1和4的血清γ球蛋白在单层培养的大鼠垂体前叶细胞中减弱了促肾上腺皮质激素释放激素诱导的ACTH释放。患者1和2的γ球蛋白降低了垂体细胞培养物中的基础TSH释放,但刺激了基础催乳素释放。这些患者的垂体激素缺乏可能是由自身免疫性疾病引起的。