Samaan N A, Stepanas A V, Danziger J, Trujillo J
Arch Intern Med. 1979 Feb;139(2):198-201.
Ten unselected patients with gonadal dysgenesis, three with Klinefelter's and seven with Turner's syndromes, were studied. Two of the patients with Klinefelter's and two with Turner's syndromes had enlarged pituitary fossae. The other six patients had normal sized sella, but showed localized change in the sellar contour on polytomography, suggesting hyperplasia or microadenoma formation of the pituitary gland. All ten patients had abnormally high serum follicle-stimulating hormone levels both at basal and after luteinizing hormone-releasing hormone stimulation. These results suggest that hyperplasia or microadenoma of the pituitary gland may occur secondary to gonadal failure, producing enlarged volume or attenuation in the normal contour of the sella turcica. Lack of awareness of reactive pituitary changes secondary to gonadal failure may result in inappropriate surgical management of what may appear to be primary pituitary tumor.
对10例未经挑选的性腺发育不全患者进行了研究,其中3例患有克兰费尔特综合征,7例患有特纳综合征。2例克兰费尔特综合征患者和2例特纳综合征患者的垂体窝增大。其他6例患者蝶鞍大小正常,但在体层摄影中显示蝶鞍轮廓有局部改变,提示垂体增生或微腺瘤形成。所有10例患者基础状态下及促黄体生成素释放激素刺激后血清促卵泡激素水平均异常升高。这些结果表明,垂体增生或微腺瘤可能继发于性腺功能衰竭,导致蝶鞍体积增大或正常轮廓变钝。对性腺功能衰竭继发的垂体反应性改变缺乏认识,可能导致对看似原发性垂体肿瘤进行不恰当的手术治疗。