Journals / Turkish Journal of Urology / 2017 / Cilt: 43 - Sayı: 4

A rare case of lobulated complete renal fusion with multiple hila and vasculature

Multipl hilum ve damarlanmalı seyrek görülen bir lobüle komplet renal füzyon olgusu

Pages
571–575
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

Though remain asymptomatic such cases warrant concomitant congenitalanomalies of other organ systems as well as the microarchitecture changes in the renal parenchyma

📌 3 Key Takeaways

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Objective & Hypothesis:Complete renal fusion without crossed renal ectopia denotes the medial fusion of the renal parenchyma (withor without changes in the microarchitecture) in the pelvis with anteriorly placed short ureters terminating intothe bladder.
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Key Findings & Data:This could be due to the failure of renal analgen to ascent, lateral migration, axial rotation, andpersistence of primitive vascular supply.
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Conclusion & Impact:Though remain asymptomatic such cases warrant concomitant congenitalanomalies of other organ systems as well as the microarchitecture changes in the renal parenchyma
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Complete renal fusion without crossed renal ectopia denotes the medial fusion of the renal parenchyma (withor without changes in the microarchitecture) in the pelvis with anteriorly placed short ureters terminating intothe bladder. This could be due to the failure of renal analgen to ascent, lateral migration, axial rotation, andpersistence of primitive vascular supply. Though remain asymptomatic such cases warrant concomitant congenitalanomalies of other organ systems as well as the microarchitecture changes in the renal parenchyma

Özet

Çapraz renal ektopinin eşlik etmediği komplet renal füzyon böbreğin mikro yapısında değişiklikler olsun veya olmasın pelviste böbrek parankiminin mediyal füzyonuyla birlikte mesane içinde sonlanan anterior yerleşimli kısa üreterleri ifade eder. Bu durum renal analgenin yükselişini, dışyana göçünü, ekseni etrafındaki rotasyonunu gerçekleştirememesine ve primitif damarsal yapının sebat etmesine bağlı olabilir. Semptom vermemelerine rağmen bu olguların eşlik eden diğer organ sistemlerinin doğuştan anomalileri ve böbrek parankimi mikro yapısındaki değişiklikler açısından değerlendirilmeleri gerekir

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Cite This Article

LC, P., DSOUZA, A. S., VARMA, A., THOMAS, H. R. (2022). A rare case of lobulated complete renal fusion with multiple hila and vasculature. Turkish Journal of Urology, Cilt: 43 - Sayı: 4, 571–575. https://ajindex.com/articles/614419

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References (2)

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