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特发性血色素沉着症中的性腺功能减退。内分泌学研究。

Hypogonadism in idiopathic hemochromatosis. Endocrine studies.

作者信息

Iyer R, Duckworth W C, Solomon S S

出版信息

Arch Intern Med. 1981 Mar;141(4):517-8.

PMID:6782964
Abstract

The mechanism of hypogonadism was studied in a 63-year-old man with idiopathic hemochromatosis. Basal levels of thyroid, prolactin, cortisol, and growth hormones were normal and responded normally to appropriate provocative stimuli. Basal testosterone and gonadotropin levels were low. There was inadequate gonadotropin response to luteinizing hormone-releasing hormone and clomiphene citrate stimulation. Testosterone response to human chorionic gonadotropin was normal. Hypothalamic-pituitary dysfunction resulting in impaired gonadotropin secretion appears to be the cause of hypogonadism in hemochromatosis.

摘要

对一名患有特发性血色素沉着症的63岁男性的性腺功能减退机制进行了研究。甲状腺激素、催乳素、皮质醇和生长激素的基础水平正常,对适当的激发刺激反应也正常。睾酮和促性腺激素的基础水平较低。促性腺激素对促黄体生成素释放激素和枸橼酸氯米芬刺激的反应不足。睾酮对人绒毛膜促性腺激素的反应正常。下丘脑 - 垂体功能障碍导致促性腺激素分泌受损似乎是血色素沉着症中性腺功能减退的原因。

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1
Hypogonadism in idiopathic hemochromatosis. Endocrine studies.特发性血色素沉着症中的性腺功能减退。内分泌学研究。
Arch Intern Med. 1981 Mar;141(4):517-8.
2
[Hypogonadism in idiopathic hemochromatosis].[特发性血色素沉着症中的性腺功能减退]
Minerva Endocrinol. 1989 Jul-Sep;14(3):159-63.
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J Endocrinol Invest. 1990 Nov;13(10):849-53. doi: 10.1007/BF03349640.
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Lowering prolactin level in a hyperprolactinemic man: responses of luteinizing hormone, follicle-stimulating hormone, and testosterone.降低高催乳素血症男性的催乳素水平:促黄体生成素、促卵泡生成素和睾酮的反应。
Arch Intern Med. 1982 Jan;142(1):146-8.
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[Erectile dysfunction and hypogonadism. Is routine endocrine screening necessary?].[勃起功能障碍与性腺功能减退。是否需要进行常规内分泌筛查?]
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引用本文的文献

1
Hypogonadotropic hypogonadism in idiopathic hemochromatosis: evidence for combined hypothalamic and pituitary involvement.特发性血色素沉着症中的低促性腺激素性性腺功能减退:下丘脑和垂体联合受累的证据
J Endocrinol Invest. 1990 Nov;13(10):849-53. doi: 10.1007/BF03349640.
2
Preclinical hypogonadism in genetic hemochromatosis in the early stage of the disease: evidence of hypothalamic dysfunction.遗传性血色素沉着症疾病早期的临床前性腺功能减退:下丘脑功能障碍的证据
J Endocrinol Invest. 1992 Jun;15(6):423-8. doi: 10.1007/BF03348765.