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Encrusted Cystitis in a Child Without Predisposing Factors: A Case Report and Literature Review
Shohei Yoshimura1,2, Kengo Hattori1, Emi Tsuji1
1Department of Pediatric Surgery, Takatsuki General Hospital, Takatsuki, JPN.
Insights
Encrusted cystitis, a rare bladder condition, was diagnosed in a child with Proteus mirabilis infection. Bladder and bowel dysfunction is suggested as a potential risk factor in pediatric cases.
Area of Science:
- Pediatric Urology
- Infectious Diseases
- Uropathology
Background:
- Encrusted cystitis is a rare condition characterized by calcification of the bladder mucosa.
- It is typically observed in immunocompromised patients, those with a history of urological interventions, or post-renal transplantation.
- Pediatric cases are exceptionally uncommon.
Observation:
- A six-year-old girl presented with rectal prolapse, urinary frequency, urinary stone drainage, and recurrent febrile urinary tract infections.
- Urinary culture identified Proteus mirabilis, and ultrasonography revealed bladder wall calcification, confirming encrusted cystitis.
- The patient lacked typical predisposing factors such as immunosuppression or prior urological procedures.
Findings:
- Treatment involved antibiotics and transurethral resection of bladder calcification.
- The patient's symptoms resolved following the intervention.
- This case highlights a potential association between bladder and bowel dysfunction and encrusted cystitis in children.
Implications:
- Bladder and bowel dysfunction should be considered as a potential risk factor for encrusted cystitis in the pediatric population.
- Further research is warranted to elucidate the pathophysiology linking bladder and bowel dysfunction to encrusted cystitis.
- This case broadens the understanding of encrusted cystitis etiology in children.
Abstract:
A six-year-old girl was admitted to our hospital with rectal prolapse, urinary frequency, urinary stone drainage, and recurrent febrile urinary tract infections. A urinary culture identified Proteus mirabilis, and an ultrasonography demonstrated mucosal calcification of the bladder wall, leading to the diagnosis of encrusted cystitis. Antibiotic administration and transurethral resection of bladder calcification were performed, and her symptoms gradually disappeared. Encrusted cystitis is extremely rare in childhood and is frequently observed in patients with post-renal transplantation, urological interventions, and immunosuppressive status. She did not have these predisposing factors; thus, bladder and bowel dysfunction may be a potential risk factor for encrusted cystitis.
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