A rare cause of neonatal hypertension: Congenital mesoblastic nephroma

被引：5

作者：

Soyaltin, Eren ^{[1
]}

Alaygut, Demet ^{[1
]}

Alparslan, Caner ^{[1
]}

Ozdemir, Tunc ^{[2
]}

Arslansoyu-Camlar, Secil ^{[1
]}

Mutlubas, Fatma ^{[1
]}

Kasap-Demir, Belde ^{[1
]}

Yavascan, Onder ^{[1
]}

机构：

[1] Tepecik Training & Res Hosp, Dept Pediat Nephrol, Izmir, Turkey

[2] Tepecik Training & Res Hosp, Dept Pediat Surg, Izmir, Turkey

来源：

TURKISH JOURNAL OF PEDIATRICS | 2018年 / 60卷 / 02期

关键词：

hypertension; newborn; mesoblastic nephroma; DIAGNOSIS; FEATURES;

D O I：

10.24953/turkjped.2018.02.014

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

A rare cause of neonatal hypertension: Congenital Mesoblastic Nephroma (CMN) is a rare renal tumor in childhood and has been reported with palpable abdominal mass, hypertension, hematuria, polyuria and hypercalcemia. Histopathologically it has been classified into two histological types: classic and cellular. We present a 32-week gestation infant and his histopathology reports of cellular CMN presented with refractory hypertension.

引用

页码：198 / 200

页数：3

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