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[继发性甲状腺功能减退伴促甲状腺激素缺乏。1例病例报告及文献复习]

[Secondary hypothyroidism with thyrotropic hormone deficiency. Presentation of a case and review of the literature].

作者信息

Foresti V, Parisio E

出版信息

Minerva Med. 1985 Dec 22;76(49-50):2323-7.

PMID:4088528
Abstract

A patient with clinical signs of hypothyroidism, low basal serum thyrotropin (TSH) and lack of response to releasing-factor (TRH) is described. The normal secretion of other anterior pituitary hormones both basal and after stimulation tests and the absence of hypophysial sella alterations found with computed axial tomography suggest the presence of a selective idiopathic TSH deficiency. The pituitary origin of this defect has been reported in literature only in five further patients, tested with TRH. The exact pathogenetic mechanism of these cases is still unknown: in the patient observed by the authors unresponsiveness both to TRH and to metoclopramide suggest an absence of TSH-producing pituitary cells or an alteration of the mechanism beyond the receptor and within the cell. However the possibility that such a secretion defect may represent a first sign of a pituitary tumor should not be excluded.

摘要

本文描述了一名患有甲状腺功能减退临床症状、基础血清促甲状腺激素(TSH)水平低且对释放因子(TRH)无反应的患者。其他垂体前叶激素在基础状态及刺激试验后的分泌正常,且计算机断层扫描未发现垂体窝改变,提示存在选择性特发性TSH缺乏。文献中仅另有5例接受TRH检测的患者报告了这种缺陷的垂体起源。这些病例的确切发病机制仍不清楚:作者观察的患者对TRH和胃复安均无反应,提示缺乏产生TSH的垂体细胞,或受体后及细胞内机制改变。然而,不应排除这种分泌缺陷可能是垂体肿瘤首发症状的可能性。

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