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隐睾症——发病机制、组织学及治疗方面

Cryptorchidism--aspects of pathogenesis, histology and treatment.

作者信息

Cortes D

机构信息

Department of Pediatric Surgery, Rigshospitalet, University of Copenhagen, Denmark.

出版信息

Scand J Urol Nephrol Suppl. 1998;196:1-54.

PMID:9561565
Abstract

Cryptorchidism is the absence of at least one testis in the scrotum. The incidence of cryptorchidism is high and almost 3% of boys in the western countries are operated on for this condition. Abnormalities in the hypothalamo-pituitary-testicular axis may result in cryptorchidism, and cryptorchidism is nearly almost present in individuals with a testis and abnormal sexual differentiation. We characterized an association of cryptorchidism and T10-S5 vertebral, renal and ureteral malformations and dysplasias. Cryptorchidism was ipsilateral to renal and ureteral malformations and dysplasias in more than 90% of cases. The association was proved with increasing frequency in: 4-10% of cryptorchid boys who had undergone laparoscopy for impalpable testes or were expected to be without additional abnormalities; 18% of cryptorchid boys in a material from a department of pediatric surgery; 34% of cryptorchid individuals who had died between week 28 and 40 of gestation; 65% of cryptorchid boys operated on for imperforate anus; all individuals with tritonmelia who are always cryptorchid. As the association was demonstrated with increasing frequency the higher the degree of abnormal differentiation of the caudal developmental field, cryptorchidism may be interpreted as a feature of such an abnormal differentiation. The general significance of our hypothesis is supported by the fact that both position and histology of the undescended testes were independent of a possible presence of the malformations and dysplasias encompassed by the association. Intra-abdominal testes were associated with persisting diaphragmatic ligaments which again were associated with an abnormal differentiation of the midline. Consequently we consider cryptorchidism a feature of abnormalities in the hypothalamo-pituitary-testicular axis and of an abnormal differentiation of the male sexual organs, the midline, and/or the caudal developmental field. The recommended age at surgery for cryptorchidism has gradually been lowered. The recommendations are mainly based on analyses of number of spermatogonia per tubular transverse section in normal and undescended testes. In 1984 when we started our investigations, the biological value of this variable was unclarified.

摘要

隐睾症是指阴囊内至少缺少一个睾丸。隐睾症的发病率很高,在西方国家,近3%的男孩因这种病症接受手术治疗。下丘脑 - 垂体 - 睾丸轴的异常可能导致隐睾症,并且隐睾症几乎总是出现在睾丸及性分化异常的个体中。我们发现隐睾症与T10 - S5椎体、肾脏及输尿管的畸形和发育异常有关。在超过90%的病例中,隐睾症与肾脏及输尿管的畸形和发育异常同侧。在以下情况中,这种关联被证实的频率越来越高:4% - 10%接受腹腔镜检查以寻找无法触及睾丸的隐睾男孩,或预计无其他异常的隐睾男孩;来自小儿外科的病例材料中,18%的隐睾男孩;妊娠第28至40周之间死亡的隐睾个体中,34%;因肛门闭锁接受手术的隐睾男孩中,65%;所有患有尾侧发育不全且总是隐睾的个体。由于随着尾侧发育区域异常分化程度越高,这种关联被证实的频率越高,因此隐睾症可被解释为这种异常分化的一个特征。我们的假设具有普遍意义,这一事实得到了支持,即未降睾丸的位置和组织学与该关联所涵盖的畸形和发育异常的可能存在无关。腹腔内睾丸与持续存在的膈肌韧带有关,而膈肌韧带又与中线的异常分化有关。因此,我们认为隐睾症是下丘脑 - 垂体 - 睾丸轴异常以及男性性器官、中线和/或尾侧发育区域异常分化的一个特征。隐睾症的推荐手术年龄已逐渐降低。这些建议主要基于对正常和未降睾丸每管横切面精原细胞数量的分析。1984年我们开始研究时,这个变量的生物学价值尚不清楚。

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