Calyceal Diverticulum: A Cystic Lesion Mimicking a Urinary Tract Infection

Calyceal diverticulum (CD) is an uncommon renal anomaly in children and often mimics other cystic lesions, making diagnosis challenging. We report the case of a nine-year-old boy evaluated during follow-up after an episode of acute pyelonephritis. He remained asymptomatic, with normal examination findings and appropriate growth. Renal ultrasound revealed a non-vascularized cystic lesion with heterogeneous content in the upper pole of the right kidney. Subsequent magnetic resonance imaging demonstrated communication with the collecting system, confirming the diagnosis of CD. While typically asymptomatic, CD may initially present with complications such as urinary tract infection (UTI). Identification relies on imaging modalities capable of visualizing the diverticular communication with the calyceal system. Management in pediatric patients is generally conservative, with surgical intervention reserved for recurrent infection, abscess formation, persistent pain, gross hematuria, or progressive enlargement. This case highlights that UTI is a complication of calyceal diverticulum and could be its first clinical manifestation. It further emphasizes the importance of including CD in the differential diagnosis of atypical pediatric renal cystic lesions and reinforces the crucial role of advanced imaging in establishing a definitive diagnosis.

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Publication Details

Journal
Cureus
Published
2025-12-17
DOI
https://doi.org/10.7759/cureus.99468
Primary Topic
Pediatric Urology and Nephrology Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Calyceal Diverticulum: A Cystic Lesion Mimicking a Urinary Tract Infection

Maria José Noruegas, Miguel Lucas, Marta Machado
Cureus
Pediatric Urology and Nephrology Studies
article

Calyceal Diverticulum: A Cystic Lesion Mimicking a Urinary Tract Infection

Maria José Noruegas, Miguel Lucas, Marta Machado
article en

Abstract

Calyceal diverticulum (CD) is an uncommon renal anomaly in children and often mimics other cystic lesions, making diagnosis challenging. We report the case of a nine-year-old boy evaluated during follow-up after an episode of acute pyelonephritis. He remained asymptomatic, with normal examination findings and appropriate growth. Renal ultrasound revealed a non-vascularized cystic lesion with heterogeneous content in the upper pole of the right kidney. Subsequent magnetic resonance imaging demonstrated communication with the collecting system, confirming the diagnosis of CD. While typically asymptomatic, CD may initially present with complications such as urinary tract infection (UTI). Identification relies on imaging modalities capable of visualizing the diverticular communication with the calyceal system. Management in pediatric patients is generally conservative, with surgical intervention reserved for recurrent infection, abscess formation, persistent pain, gross hematuria, or progressive enlargement. This case highlights that UTI is a complication of calyceal diverticulum and could be its first clinical manifestation. It further emphasizes the importance of including CD in the differential diagnosis of atypical pediatric renal cystic lesions and reinforces the crucial role of advanced imaging in establishing a definitive diagnosis.

CureusVol. 17(12)
Hospitais da Universidade de Coimbra (PT), Escola Superior de Tecnologia da Saúde de Coimbra (PT), University of Coimbra (PT)
Openalex Percentile: Top 50%
Pediatric Urology and Nephrology Studies
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