Congenital scrotal agenesis with bilateral cryptorchidism: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Mohammad Sharif Sediqi, Abdulwali Wali, Khatera Habib, Khesrow Ekram, Abdulhai Wali
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引用次数: 0

Abstract

Background: The disorder known as congenital scrotal agenesis is an extremely rare condition. In the literature, 11 cases of congenital scrotal agenesis or absence have been reported thus far. Most of them are bilateral and contain cryptorchidism. In a rare case of bilateral cryptorchidism, we report a 36-day-old Afghan infant who presented to Maiwand Teaching Hospital with fever and vomiting due to infection and congenital scrotal agenesis. The diagnosis of these anomalies was made using clinical and laboratory results, with the clinical characteristics being recorded during the sixth week of life. After receiving therapy for sepsis, he was referred to the pediatric surgical department in good health. Given that the parents of the congenital scrotal agenesis reference case were consanguineous, there may have been a genetic component to the development of the condition.

Case presentation: We describe a rare instance of bilateral cryptorchidism, with congenital scrotal agenesis in a 36-day-old Afghan baby that had come to Maiwand teaching hospital for fever and vomiting on the basis of sepsis. The clinical characteristics were noted during the sixth week of life and clinical and laboratory results were used to determine the diagnosis of these anomalies. He was referred to the pediatric surgery department in good health following the treatment for sepsis. Given that the reference case of congenital scrotal agenesis had consanguineous parents, a link to genetics may have contributed to the disease's emergence.

Conclusion: Congenital scrotal agenesis is an incredibly uncommon condition of urological congenital disorder. To date, the literature has reported 11 cases of congenital scrotal agenesis or absence, most of which are bilateral and involve cryptorchidism. This case presents another human being that suffers congenitally from scrotal agenesis with bilateral cryptorchidism who was born in Kabul city of Afghanistan from a multigravida mother who has positive consanguinity to her husband.

先天性阴囊发育不全伴双侧隐睾1例。
背景:先天性阴囊发育不全是一种极为罕见的疾病。在文献中,11例先天性阴囊发育不全或缺失已被报道到目前为止。大多数是双侧的,包含隐睾。在一个罕见的病例双侧隐睾,我们报告一个36天的阿富汗婴儿谁提出了发烧和呕吐,由于感染和先天性阴囊发育不全。这些异常的诊断是使用临床和实验室结果,并在生命的第六周记录临床特征。在接受败血症治疗后,他被转介到儿科外科,身体状况良好。鉴于先天性阴囊发育不全参考病例的父母是近亲,可能有遗传成分的发展条件。病例介绍:我们描述了一个罕见的病例双侧隐睾,先天性阴囊发育不全在一个36天的阿富汗婴儿来Maiwand教学医院发烧和呕吐的基础上败血症。在生命的第六周记录临床特征,并使用临床和实验室结果来确定这些异常的诊断。他在接受败血症治疗后健康状况良好,被转介到儿科外科。考虑到先天性阴囊发育不全的参考病例有近亲父母,与遗传的联系可能促成了疾病的出现。结论:先天性阴囊发育不全是一种极为罕见的泌尿系统先天性疾病。迄今为止,文献报道了11例先天性阴囊发育不全或缺失,其中大多数是双侧和涉及隐睾。本病例介绍了另一个患有先天性阴囊发育不全并双侧隐睾的人,他出生在阿富汗喀布尔市,来自一位与丈夫有阳性血亲关系的多胎母亲。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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