首页> 美国卫生研究院文献>Bosnian Journal of Basic Medical Sciences >CLINICAL DILEMMAS AND SURGICAL TREATMENT OF PENOSCROTAL SCROTAL AND PERINEAL HYPOSPADIAS
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CLINICAL DILEMMAS AND SURGICAL TREATMENT OF PENOSCROTAL SCROTAL AND PERINEAL HYPOSPADIAS

机译:硬结膜炎巩膜炎和会阴性血尿不足的临床诊断和外科治疗

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摘要

Hypospadia is the most common congenital malformation of the urinary tract. It is a malformation with the opening of the urethra proximally from the usual site. The meatal opening can be anywhere alone the shaft of the penis, or in more severe forms, within the scrotum, or in the perineum. Consequently the hypospadias can be distal, medial and proximal. The proximal ones can be penoscrotal (PS), scrotal (SC) and perineal (PE). The cause of hypospadias is largely unknown; however, current epidemiol-ogy and laboratory studies have shed new light into the etiology of hypospadias. With recent advance-ments in molecular biology, microarray technology, it appears that hypospadias is potentially related to disrupted gene expression. Currently, the only available treatment is surgery. The aim of this study was to present our results of the surgical correction of hypospadias and methods used to answer the clinical dilemmas about the gender. Authors have used two methods for a surgical resolution of the hypospadia - one-step operation suggested by Snodgrass and two-step operation, employing free graft suggested by Bracka. Clinical dilemmas regarding the gender were answered using cytogenetic assessment through lymphocyte cultivation method, suggested by Seabright. The cytogenetic assessment was carried in 23 patients with proximal hypospadia (penoscrotal, scrotal and perineal). Characteristic male cariotype (46, XY) was found in 22 patients. In one patient, with scrotal hypospadia, we found the characteristic female cariotype. This patient had testicles. The patient with female cariotype had a TDG gene that determines the differentiation of the testicles. Although surgery remains the only therapy for the treatment of the hypospadias, better understanding of the molecular and hormonal mechanisms behind the diseases may contribute to the prevention and the decrease in the incidence of the malformation. Cytogenetic testing in patients with unclear gender is important in planning further treatment.
机译:下丘脑是最常见的先天性泌尿道畸形。这是一种畸形,尿道开口位于通常部位的近端。肉的开口可以在阴茎杆的任何地方,也可以是阴囊内或会阴处更严重的形式。因此,尿道下裂可以在远端,中间和近端。近端可以是阴囊(PS),阴囊(SC)和会阴(PE)。尿道下裂的原因在很大程度上尚不清楚;然而,当前的流行病学和实验室研究为尿道下裂的病因学提供了新的思路。随着分子生物学,微阵列技术的最新进展,尿道下裂似乎与基因表达的破坏有关。当前,唯一可用的治疗方法是手术。这项研究的目的是介绍我们的尿道下裂矫正术的结果以及用于回答有关性别的临床难题的方法。作者使用两种方法来解决尿道下裂的手术方法-Snodgrass建议采用一步手术,而Bracka建议采用游离移植进行两步手术。 Seabright建议,通过淋巴细胞培养方法进行细胞遗传学评估,以解决有关性别的临床难题。对23名尿道下裂近端(阴囊,阴囊和会阴)患者进行了细胞遗传学评估。在22例患者中发现了特征性的男性心脏型(46,XY)。在一名患有阴囊尿道下裂的患者中,我们发现了特征性的女性心脏型。该患者有睾丸。具有女性心脏型的患者具有决定睾丸分化的TDG基因。尽管外科手术仍然是治疗尿道下裂的唯一疗法,但对疾病背后的分子和激素机制的更好理解可能有助于预防和减少畸形的发生。性别不明的患者进行细胞遗传学检测对于计划进一步治疗很重要。

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