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...
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Main Authors: | , , , , , |
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Format: | Book |
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Frontiers Media S.A.,
2022-11-01T00:00:00Z.
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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. |
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Item Description: | 2296-2360 10.3389/fped.2022.1040304 |