Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: A case report and literature review

BackgroundCongenital mesoblastic nephroma (CMN) is a rare renal tumour in children, the most common kidney tumour in the neonatal period. It can be divided into three types, classical, cellular and mixed.Case presentationA 31-year-old Chinese woman had no apparent foetal abnormality in regular prena...

Full description

Saved in:
Bibliographic Details
Main Authors: Xiaoxiao Zhang (Author), Huijing Zhang (Author), Shuang Wang (Author), Yangxu Gao (Author), Li Liang (Author), Huixia Yang (Author)
Format: Book
Published: Frontiers Media S.A., 2022-11-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:BackgroundCongenital mesoblastic nephroma (CMN) is a rare renal tumour in children, the most common kidney tumour in the neonatal period. It can be divided into three types, classical, cellular and mixed.Case presentationA 31-year-old Chinese woman had no apparent foetal abnormality in regular prenatal care during the first and second trimesters. At 33 weeks of gestation, a solid mass in the right kidney was noted with echoes similar to liver and hypervascularity. It grew larger during late pregnancy. The infant was transferred to have a radical nephrectomy on the 9th day after birth. The postoperative histopathological result indicated classical CMN.ConclusionCMN could be detected prenatally, mainly during late pregnancy. The postnatal outcome is good.
Item Description:2296-2360
10.3389/fped.2022.1040304