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原发性甲状腺功能减退症和垂体功能不全。

Primary hypothyroidism and pituitary insufficiency.

作者信息

Gluck F B, Nusynowitz M L, Montgomery M

出版信息

South Med J. 1978 Dec;71(12):1521-3. doi: 10.1097/00007611-197812000-00022.

Abstract

A 40-year-old man with primary hypothyroidism and sellar enlargement is described. There was deficiency of all pituitary tropic hormones except TSH which was elevated. TRH stimulation revealed responsiveness of pituitary thyrotropic cells, and thyroxine administration suppressed the elevated TSH. These findings are compatible with either a TSH-producing chromophobe adenoma resulting from primary hypothyroidism or, because of the suppressibility of the TSH secretion, thyrotropic hyperplasia secondary to hypothyroidism maintaining TSH secretion in the face of a non-TSH-secreting pituitary tumor.

摘要

本文描述了一名患有原发性甲状腺功能减退和蝶鞍扩大的40岁男性。除促甲状腺激素(TSH)升高外,所有垂体促激素均缺乏。促甲状腺激素释放激素(TRH)刺激显示垂体促甲状腺细胞有反应,给予甲状腺素可抑制升高的TSH。这些发现与原发性甲状腺功能减退导致的分泌TSH的嫌色细胞瘤相符,或者由于TSH分泌的可抑制性,与甲状腺功能减退继发的促甲状腺细胞增生相符,即在存在非分泌TSH的垂体肿瘤时维持TSH分泌。

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