Aya Mohamed Nasr Ibrahim , Mohab Alsaid Saad , Mustafa I. Al-Shalah , Zaid F. Altawallbeh , Abdelrahman Elkhiat , Mohamed Elsaqa , Hasan Ahmad Matar , Akhmad Asaad Matar , Mostafa Said
{"title":"迟发不完全膀胱重复:意外误诊罕见病例报告","authors":"Aya Mohamed Nasr Ibrahim , Mohab Alsaid Saad , Mustafa I. Al-Shalah , Zaid F. Altawallbeh , Abdelrahman Elkhiat , Mohamed Elsaqa , Hasan Ahmad Matar , Akhmad Asaad Matar , Mostafa Said","doi":"10.1016/j.eucr.2025.103074","DOIUrl":null,"url":null,"abstract":"<div><div>Incomplete bladder duplication (BD) is a rare congenital anomaly in which two bladder halves remain partially connected and share a single urethra; only 12 cases have been recorded. A 60-year-old female with severe lower urinary tract symptoms (LUTS) following hysterectomy and sacrocolpopexy. Initially suspected to be mesh-related, cystourethroscopy and MRI revealed an incomplete sagittal bladder septum. Laser excision resolved her symptoms. While surgery is rarely needed for BD, this case underscores its necessity in symptomatic patients. This case of incomplete BD without associated multiple congenital malformations emphasizes the need to consider rare congenital anomalies even in atypical presentation.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"61 ","pages":"Article 103074"},"PeriodicalIF":0.5000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report\",\"authors\":\"Aya Mohamed Nasr Ibrahim , Mohab Alsaid Saad , Mustafa I. Al-Shalah , Zaid F. Altawallbeh , Abdelrahman Elkhiat , Mohamed Elsaqa , Hasan Ahmad Matar , Akhmad Asaad Matar , Mostafa Said\",\"doi\":\"10.1016/j.eucr.2025.103074\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Incomplete bladder duplication (BD) is a rare congenital anomaly in which two bladder halves remain partially connected and share a single urethra; only 12 cases have been recorded. A 60-year-old female with severe lower urinary tract symptoms (LUTS) following hysterectomy and sacrocolpopexy. Initially suspected to be mesh-related, cystourethroscopy and MRI revealed an incomplete sagittal bladder septum. Laser excision resolved her symptoms. While surgery is rarely needed for BD, this case underscores its necessity in symptomatic patients. This case of incomplete BD without associated multiple congenital malformations emphasizes the need to consider rare congenital anomalies even in atypical presentation.</div></div>\",\"PeriodicalId\":38188,\"journal\":{\"name\":\"Urology Case Reports\",\"volume\":\"61 \",\"pages\":\"Article 103074\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-05-19\",\"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/S2214442025001457\",\"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/S2214442025001457","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Late presentation of incomplete bladder duplication: an unexpected misdiagnosed rare case report
Incomplete bladder duplication (BD) is a rare congenital anomaly in which two bladder halves remain partially connected and share a single urethra; only 12 cases have been recorded. A 60-year-old female with severe lower urinary tract symptoms (LUTS) following hysterectomy and sacrocolpopexy. Initially suspected to be mesh-related, cystourethroscopy and MRI revealed an incomplete sagittal bladder septum. Laser excision resolved her symptoms. While surgery is rarely needed for BD, this case underscores its necessity in symptomatic patients. This case of incomplete BD without associated multiple congenital malformations emphasizes the need to consider rare congenital anomalies even in atypical presentation.