Naser El-Mefleh , Hassan Al-Hussein , Ebrahem Othman , Hasan Darwish , Mohammad Alsaleh
{"title":"新生儿副阴囊:罕见的先天性阴囊异常","authors":"Naser El-Mefleh , Hassan Al-Hussein , Ebrahem Othman , Hasan Darwish , Mohammad Alsaleh","doi":"10.1016/j.eucr.2025.103021","DOIUrl":null,"url":null,"abstract":"<div><div>Accessory scrotum (AS) is an extremely rare congenital anomaly, defined as scrotal-like tissue outside a normal anatomical location, without associated testes. It is often associated with perineal lipomas and other anomalies. We report a newborn male with a scrotum-like perineal mass posterior to the original scrotum. Postnatal assessment revealed a perineal mass resembling an AS. Ultrasound and CT confirmed a fat-containing mass, ruling out teratoma. A cystoscopy confirmed urinary tract integrity, and complete surgical excision of AS was conducted successfully. Although benign, AS presents a diagnostic challenge and may mimic other perineal anomalies. Complete resection is curative.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"60 ","pages":"Article 103021"},"PeriodicalIF":0.5000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Accessory scrotum in neonate: A rare congenital scrotal anomaly\",\"authors\":\"Naser El-Mefleh , Hassan Al-Hussein , Ebrahem Othman , Hasan Darwish , Mohammad Alsaleh\",\"doi\":\"10.1016/j.eucr.2025.103021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Accessory scrotum (AS) is an extremely rare congenital anomaly, defined as scrotal-like tissue outside a normal anatomical location, without associated testes. It is often associated with perineal lipomas and other anomalies. We report a newborn male with a scrotum-like perineal mass posterior to the original scrotum. Postnatal assessment revealed a perineal mass resembling an AS. Ultrasound and CT confirmed a fat-containing mass, ruling out teratoma. A cystoscopy confirmed urinary tract integrity, and complete surgical excision of AS was conducted successfully. Although benign, AS presents a diagnostic challenge and may mimic other perineal anomalies. Complete resection is curative.</div></div>\",\"PeriodicalId\":38188,\"journal\":{\"name\":\"Urology Case Reports\",\"volume\":\"60 \",\"pages\":\"Article 103021\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Urology Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214442025000920\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214442025000920","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Accessory scrotum in neonate: A rare congenital scrotal anomaly
Accessory scrotum (AS) is an extremely rare congenital anomaly, defined as scrotal-like tissue outside a normal anatomical location, without associated testes. It is often associated with perineal lipomas and other anomalies. We report a newborn male with a scrotum-like perineal mass posterior to the original scrotum. Postnatal assessment revealed a perineal mass resembling an AS. Ultrasound and CT confirmed a fat-containing mass, ruling out teratoma. A cystoscopy confirmed urinary tract integrity, and complete surgical excision of AS was conducted successfully. Although benign, AS presents a diagnostic challenge and may mimic other perineal anomalies. Complete resection is curative.