Lamesch A
Service de Chirurgie pédiatrique, Centre hospitalier, Luxembourg.
Chirurgie. 1992;118(5):328-32; discussion 333.
Monorchidism is a Testicular Regression Syndrome (Vanishing Testis Syndrome), defined as the unilateral or bilateral partial and complete absence of testicular tissue with or without rudimentary epididymal and spermatic cord remnants in the presence of normal duct development and normal external genitalia. In this paper we report the results of a personal series of 36 patients. We discuss the histopathology and try to answer the question whether protection of the solitary contralateral testis by orchidopexy is necessary in monorchidism. Our results suggest that a fixation of the contralateral testis is not necessary in children operated on for monorchidism. The histopathological findings provide a support for the concept of in utero torsion of the testis as the basis for the Testicular Regression Syndrome. These findings are characteristic, if non-specific. Vas deferens, epididymis, calcification or hemosiderin pigmentation was noted in almost 90% of the cases. In the absence of these remnants clinical and surgical findings and the presence of a richly vascular stroma supported the diagnosis.
单睾症是一种睾丸退化综合征(隐睾综合征),定义为单侧或双侧部分或完全缺乏睾丸组织,伴有或不伴有附睾和精索残迹,而导管发育和外生殖器正常。在本文中,我们报告了一组36例患者的个人研究结果。我们讨论了组织病理学,并试图回答在单睾症中通过睾丸固定术保护对侧孤立睾丸是否必要的问题。我们的结果表明,对于因单睾症接受手术的儿童,对侧睾丸固定术并非必要。组织病理学发现为睾丸在子宫内扭转作为睾丸退化综合征基础的概念提供了支持。这些发现虽不具特异性,但具有特征性。在近90%的病例中发现了输精管、附睾、钙化或含铁血黄素沉着。在没有这些残迹的情况下,临床和手术发现以及丰富的血管基质支持诊断。