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下丘脑性垂体功能减退症患儿的血浆促甲状腺激素升高及甲状腺功能减退

Elevated plasma TSH and hypothyroidism in children with hypothalamic hypopituitarism.

作者信息

Illig R, Krawczyńska H, Torresani T, Prader A

出版信息

J Clin Endocrinol Metab. 1975 Oct;41(4):722-8. doi: 10.1210/jcem-41-4-722.

Abstract

Basal TSH levels were found to be elevated in 6 patients with documented growth hormone deficiency and hypothyroidism. TRH (200 mug/m2 administered intravenously) led to an exaggerated TSH response. This is in contrast to the results in other GH-deficient children, with either a delayed rise of TSH (hypothalamic hypothyroidism due to TRH deficiency, n = 22), an absent TSH response (pituitary hypothyroidism due to TSH deficiency, n = 7), or a normal increase of TSH (isolated GH deficiency, n = 20). Elevated plasma TSH in the presence of hypothyroidism as seen in 6 of our patients with idiopathic hypopituitarism or craniopharyngioma, indicates an intact feedback action between the pituitary and the thyroid gland. TSH, however, seems to be inadequate for the maintenance of normal thyroid function. It is suggested that in certain patients with hypothalamic disorders, TSH is secreted in a biologically less active form.

摘要

在6例已确诊生长激素缺乏和甲状腺功能减退的患者中,发现基础促甲状腺激素(TSH)水平升高。促甲状腺激素释放激素(TRH,静脉注射剂量为200μg/m²)导致TSH反应过度。这与其他生长激素缺乏儿童的结果相反,其他儿童要么TSH升高延迟(由于TRH缺乏导致的下丘脑性甲状腺功能减退,n = 22),要么TSH无反应(由于TSH缺乏导致的垂体性甲状腺功能减退,n = 7),要么TSH正常升高(单纯生长激素缺乏,n = 20)。在我们6例特发性垂体功能减退或颅咽管瘤患者中,存在甲状腺功能减退时血浆TSH升高,表明垂体和甲状腺之间存在完整的反馈作用。然而,TSH似乎不足以维持正常的甲状腺功能。提示在某些下丘脑疾病患者中,TSH以生物活性较低的形式分泌。

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