Grabski J, Pusch H, Schirren C, Passarge E, Held K, Bartsch W, Wernicke I
Andrologia. 1979 May-Jun;11(3):182-96.
In a clinical study 101 patients with Klinefelter's syndrome (Kl. sy.) are evaluated. Clinical, endocrinological and histometrical aspects were of main interest. The results were compared with a group of patients with azoospermia by obstruction. The statistical evaluation showed significant differences concerning body-height, volume of ejaculate, size of testis, and the concentration of FSH and LH in serum. Histometrical investigations showed significant differences for the diameter of seminiferous tubules and their wall-thickness. The various degrees of Leydig-cell-increase at Kl. Sy. are described as--increased--excessively increased--and adenomalike. Sex-Chromatin was found positive in 62 of 64 cases of Klinefelter's syndrome, verified by chromosome analysis. The number of Barr-bodies ranged from 1-45 (200 cells evaluated) x mean was 9,6. The analysis of chromosomes in 64 cases showed a karyotype of 47,XXY in 59 cases, a 46, XY/47,XXY mosaic in 4 cases and 46,XX/46,XY/47,XXY mosaic in 1 case. The discussion pointed out, that Kl. sy. has no typical, but a variety of symptoms. The position of the evaluation of sex-chromatin for diagnosis and the possibilities of errors are discussed. The problem of fertility in Kl. sy. is mentioned, as we found two cases with complete spermatogenesis, yet with azoospermia, among our patients. The pathogenesis of the characteristical histological changes in testis with Kl. sy. remains open. The mechanism which may lead to the striking increase of Leydig-cells is discussed.
在一项临床研究中,对101例克兰费尔特综合征(Kl. sy.)患者进行了评估。主要关注临床、内分泌和组织计量学方面。将结果与一组因梗阻导致无精子症的患者进行了比较。统计评估显示,在身高、射精量、睾丸大小以及血清中促卵泡生成素(FSH)和促黄体生成素(LH)浓度方面存在显著差异。组织计量学研究显示,曲细精管直径及其管壁厚度存在显著差异。克兰费尔特综合征中不同程度的莱迪希细胞增生被描述为——增加——过度增加——以及腺瘤样。在64例克兰费尔特综合征患者中,有62例性染色质呈阳性,经染色体分析证实。巴氏小体数量在1 - 45之间(评估了200个细胞),平均值为9.6。对64例患者的染色体分析显示,59例核型为47,XXY,4例为46,XY/47,XXY嵌合体,1例为46,XX/46,XY/47,XXY嵌合体。讨论指出,克兰费尔特综合征没有典型症状,而是有多种症状。讨论了性染色质评估在诊断中的地位以及可能出现的错误。提到了克兰费尔特综合征患者的生育问题,因为在我们的患者中发现了2例完全精子发生但无精子症的病例。克兰费尔特综合征患者睾丸特征性组织学变化的发病机制尚不清楚。讨论了可能导致莱迪希细胞显著增加的机制。