Jenkins J S, Gilbert C J, Ang V
J Clin Endocrinol Metab. 1976 Aug;43(2):394-9. doi: 10.1210/jcem-43-2-394.
Hypothalamic-pituitary function was investigated in 20 patients with craniopharyngioma, and all showed some degree of hypopituitarism. Pituitary-adrenal dysfunction was present in 50% of the patients whereas all but one had deficiencies of growth hormone and gonadotropin. Serum thyroxine was low in 13 patients, and in a further six there was an abnormal response of thyrotropin (TSH) to thyrotropin-releasing hormone (TRH). Prolactin levels were normal in over half the patients tested and only moderately elevated in the remainder. Gonadotropins failed to increase adequately after gonadotropin-releasing hormone (LRH) in all but one patient, and the response gave no indication of the predominantly hypothalamic site of the tumors.
对20例颅咽管瘤患者的下丘脑 - 垂体功能进行了研究,所有患者均表现出一定程度的垂体功能减退。50%的患者存在垂体 - 肾上腺功能障碍,而除1例患者外,所有患者均有生长激素和促性腺激素缺乏。13例患者血清甲状腺素水平低,另有6例促甲状腺激素(TSH)对促甲状腺激素释放激素(TRH)的反应异常。超过一半接受检测的患者催乳素水平正常,其余患者仅中度升高。除1例患者外,所有患者在促性腺激素释放激素(LRH)后促性腺激素均未充分增加,且该反应未显示肿瘤主要位于下丘脑部位。