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Journals / Pediatric Urology Case Reports / 2020 / Cilt: 7 - Sayı: 2

Cloacal dysgenesis sequence with bilateral renal agenesis, bladder agenesis, pulmonary hypoplasia and left choanal atresia: A case report

Esra OZCAKİR
Sefer Tolga OKAY
İpek GÜNEY VARAL
Mete KAYA
Pages
56–59
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A case of posterior urethral valve is described with multiple urethroperineal fistulas.
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Key Findings & Data:This association is extremely rare.
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Conclusion & Impact:On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

A case of posterior urethral valve is described with multiple urethroperineal fistulas. This association is extremely rare. The crucial point in the diagnosis is to distinguish these fistulas from the urethral duplications that actually guide the treatment. The presence of these fistulas in patients with posterior urethral valve may have a beneficial effect on renal function as it reduces the pressure on the bladder. On the other hand, incomplete valve ablation may contribute to the recurrence of the fistula.

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Cite This Article

OZCAKİR, E., OKAY, S. T., VARAL, İ. G., KAYA, M. (2020). Cloacal dysgenesis sequence with bilateral renal agenesis, bladder agenesis, pulmonary hypoplasia and left choanal atresia: A case report. Pediatric Urology Case Reports, Cilt: 7 - Sayı: 2, 56–59. https://ajindex.com/articles/285541

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