Dermoid cyst associated with segmental multicystic renal dysplasia: A rare case

IF 0.5 Q4 UROLOGY & NEPHROLOGY Urology Case Reports Pub Date : 2025-02-09 DOI:10.1016/j.eucr.2025.102980
Syrine Laribi , Marwa Messaoud , Manel Njima , Mabrouk Abdelali , Samia Belhassen , Afef Toumi , Mongi Mekki , Lassaad Sahnoun
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引用次数: 0

Abstract

Most multicystic dysplastic kidneys (MCDKs) are detected prenatally, yet there is no clear consensus on initial evaluation and follow-up. We report the case of a 4-year-old male diagnosed with right pyelocalyceal dilation in utero, confirmed postnatally as MCDK. Follow-up ultrasounds revealed rapid growth of three upper pole cysts, reaching 8 cm. A right upper pole nephrectomy was performed, and histopathology revealed a renal dermoid cyst within segmental multicystic renal dysplasia. This case highlights the critical role of postnatal imaging and follow-up in detecting atypical features, including rare entities like intrarenal teratomas, enabling timely surgical intervention and improved outcomes.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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