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总结21例IHH的临床特点、激素水平、甲状腺和肾上腺皮质功能及部分病例的hCG、LH-RH刺激试验结果。21例IHH中SHH占16例,合并生长激素缺乏5例。有先天性缺陷者13例。除PRL外,所测垂体-性腺轴系其他激素均明显低于正常男性。IHH患者对hCG刺激反应差,对LH-RH刺激无反应。4例矮小者对胰岛素低血糖和/或L-dopa刺激均无反应。结合典型病例介绍了本病的诊断与治疗方法。
Summary of 21 cases of IHH clinical features, hormone levels, thyroid and adrenal function and some cases of hCG, LH-RH stimulation test results. SHH in 21 cases of IHH accounted for 16 cases, combined with growth hormone deficiency in 5 cases. 13 cases of congenital defects. In addition to PRL, the measured pituitary - gonadal axis of other hormones were significantly lower than normal men. IHH patients responded poorly to hCG stimulation and did not respond to LH-RH stimulation. Four cases of short persons had no response to hypoglycemia and / or L-dopa stimulation. Combined with typical cases of the diagnosis and treatment of this disease.