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异位阴囊及阴茎阴囊转位:病例报告与文献综述

Ectopic scrotum and penoscrotal transposition: Case report and literature review.

作者信息

Huang Haoran, Liu Xiangxia, Li Zuoqing, Lin Junjie, Yang Hai, Xu Zhe

机构信息

Department of Pediatric Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Department of Plastic Surgery, University of Tennessee Health Science Center, Memphis, TN, United States.

出版信息

Front Pediatr. 2023 Feb 21;11:1015384. doi: 10.3389/fped.2023.1015384. eCollection 2023.

DOI:10.3389/fped.2023.1015384
PMID:36896407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9989158/
Abstract

BACKGROUND

Ectopic scrotum (ES) is an extremely rare congenital scrotal malformation. Ectopic scrotum with VATER/VACTERL [vertebral defects (V), anal atresia or anorectal malformations (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), cardiac defects, renal malformations (R), and limb defects (L)] association is even rarer. There are no uniform guidelines for diagnosis and treatment.

CLINICAL CASE

We described a 2-year-5-month-old boy who has ectopic scrotum and penoscrotal transposition and reviewed relevant literature in this report. We performed laparoscopy exploration, rotation flap scrotoplasty, and orchiopexy and achieved a great result during the postoperative follow-up.

CONCLUSIONS

Combined with the previous literature, we made a summary to come up with a plan for the diagnosis and treatment of ectopic scrotum. Rotation flap scrotoplasty and orchiopexy are worthy of considering operative methods in treating ES. For penoscrotal transposition or VATER/VACTERL association, we can treat the diseases individually.

摘要

背景

异位阴囊(ES)是一种极其罕见的先天性阴囊畸形。伴有VATER/VACTERL[脊柱缺陷(V)、肛门闭锁或肛门直肠畸形(A)、心脏缺陷(C)、伴有或不伴有食管闭锁的气管食管瘘(TE)、心脏缺陷、肾脏畸形(R)和肢体缺陷(L)]综合征的异位阴囊更为罕见。目前尚无统一的诊断和治疗指南。

临床病例

我们在本报告中描述了一名2岁5个月大患有异位阴囊和阴茎阴囊转位的男孩,并回顾了相关文献。我们进行了腹腔镜探查、旋转皮瓣阴囊成形术和睾丸固定术,术后随访取得了良好效果。

结论

结合既往文献,我们进行了总结,提出了异位阴囊的诊断和治疗方案。旋转皮瓣阴囊成形术和睾丸固定术是治疗ES值得考虑的手术方法。对于阴茎阴囊转位或VATER/VACTERL综合征,我们可以分别治疗这些疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/ce19a9a01b42/fped-11-1015384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/74240e9175ea/fped-11-1015384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/24af7e4574b8/fped-11-1015384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/ce19a9a01b42/fped-11-1015384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/74240e9175ea/fped-11-1015384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/24af7e4574b8/fped-11-1015384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212a/9989158/ce19a9a01b42/fped-11-1015384-g003.jpg

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A Case of Ectopic Scrotum with Inconspicuous Penis.
Fetal Pediatr Pathol. 2023 Apr;42(2):307-309. doi: 10.1080/15513815.2022.2094512. Epub 2022 Jun 30.
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Synchronous Development of Hemiscrotal Tissue in the Orthotopic and Ectopic Locations in Association with other Urological Anomalies.阴囊半侧组织在原位和异位位置与其他泌尿系统异常的同步发育。
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Analysis of Associated Anomalies in Anorectal Malformation: Major and Minor Anomalies.肛门直肠畸形相关畸形分析:主要畸形和次要畸形。
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Accessory Scrotum.副阴囊
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One stage rotation flap scrotoplasty and orchidopexy for the correction of ectopic scrotum: A case report.一期旋转皮瓣阴囊成形术及睾丸固定术矫正异位阴囊:一例报告
Urol Case Rep. 2019 Apr 10;25:100886. doi: 10.1016/j.eucr.2019.100886. eCollection 2019 Jul.
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[Ectopias of the kidney, urinary tract organs, and male genitalia. German version.].[肾脏、尿路器官及男性生殖器异位。德文版。]
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Ectopic Scrotum with VACTERL Association.伴有VACTERL综合征的异位阴囊
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Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.VATER/VACTERL综合征的潜在遗传因素,特别关注“肾脏”表型
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