✨
AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
We present a 32-week gestation infant and his histopathologyreports of cellular CMN presented with refractory hypertension.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:A rare cause of neonatal hypertension: Congenital Mesoblastic Nephroma(CMN) is a rare renal tumor in childhood and has been reported withpalpable abdominal mass, hypertension, hematuria, polyuria and hypercalcemia.Histopathologically it has been classified into two histological types: classicand cellular.
📊
Key Findings & Data:A rare cause of neonatal hypertension: Congenital Mesoblastic Nephroma(CMN) is a rare renal tumor in childhood and has been reported withpalpable abdominal mass, hypertension, hematuria, polyuria and hypercalcemia.Histopathologically it has been classified into two histological types: classicand cellular.
💡
Conclusion & Impact:We present a 32-week gestation infant and his histopathologyreports of cellular CMN presented with refractory hypertension.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
A rare cause of neonatal hypertension: Congenital Mesoblastic Nephroma(CMN) is a rare renal tumor in childhood and has been reported withpalpable abdominal mass, hypertension, hematuria, polyuria and hypercalcemia.Histopathologically it has been classified into two histological types: classicand cellular. We present a 32-week gestation infant and his histopathologyreports of cellular CMN presented with refractory hypertension.
🔖
Cite This Article
Alparslan, C., Kasap-Demir, B., Mutlubaş, F., Yavaşcan, Ö., Çamlar, S. A., Soyaltın, E., Alaygut, D., Özdemir, T. (2022). A rare cause of neonatal hypertension: Congenital mesoblastic nephroma. Turkish Journal of Pediatrics, Cilt: 60 - Sayı: 2, 198–200. https://ajindex.com/articles/613137