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Eosinophilic cystitis in a 4-year-old boy: successful long-term treatment with cyclosporin A
A Pomeranz1, A Eliakim, Y Uziel
1Department of Pediatrics, Meir General Hospital, Sapir Medical Center, Kfar Saba, Israel. avip2@clalit.org.il
Insights
A rare bladder tumor-forming eosinophilic cystitis in a child was successfully treated with cyclosporin A. This immunosuppressive therapy led to a complete cure, offering hope for similar rare pediatric bladder conditions.
Area of Science:
- Pediatric Urology
- Oncology
- Immunology
Background:
- Tumor-forming eosinophilic cystitis is a rare and poorly understood bladder lesion.
- Pediatric bladder masses require careful diagnosis and management.
- Standard treatments for eosinophilic cystitis have shown limited efficacy.
Observation:
- A 4-year-old boy presented with severe lower urinary tract symptoms and a bladder mass.
- Initial treatments including antiparasitic medication and high-dose corticosteroids were ineffective.
- The child's condition progressively worsened despite conventional therapies.
Findings:
- Biopsy confirmed tumor-forming eosinophilic cystitis.
- Cyclosporin A treatment for 8 months resulted in a complete clinical, radiologic, and histopathologic cure.
- No adverse side effects were observed during or after cyclosporin A therapy.
Implications:
- Cyclosporin A represents a potential novel therapeutic option for refractory tumor-forming eosinophilic cystitis in children.
- This case highlights the importance of considering alternative immunosuppressive treatments for rare pediatric bladder conditions.
- Further research is warranted to elucidate the pathogenesis and optimize treatment strategies for eosinophilic cystitis.
Abstract:
A 4-year-old Jewish boy presented with dysuria, urinary dribbling, increased urinary frequency, and new onset of diurnal enuresis. An infiltrating solid mass involving the entire bladder wall was found. Biopsy revealed "tumor-forming" eosinophilic cystitis, a rare bladder lesion of unclear cause. Antitoxocariasis treatment was unsuccessful. High-dose corticosteroids failed. The child's clinical condition and bladder sonographic findings continued to deteriorate. Treatment with cyclosporin A was given for 8 months, with a complete clinical, radiologic, and histopathologic cure and no side effects. Two years of follow-up showed a complete recovery.
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