| Literature DB >> 14634980 |
Wen-Yin Chen1, Ching-Nan Lin, Chien-Shun Chao, Mike Yan-Sheng Lin, Chee-Wai Mak, Shih-Sung Chuang, Ching-Cherng Tzeng, Kuo-Feng Huang.
Abstract
Although congenital mesoblastic nephroma (CMN) is a rare benign congenital renal tumor, it is the most common solid renal tumor in the newborn period. The most common presentation of congenital mesoblastic nephroma is polyhydramnios, and only one case with prenatal fetal hydrops has been previously reported. Prenatal diagnosis of CMN has previously been made on the basis of the findings of sonography in the third trimester, and magnetic resonance imaging (MRI)-based diagnosis has been reported recently. Here we report a case of prenatally diagnosed classical type CMN diagnosed at 22 + 3 weeks of gestation based on the findings of sonography and magnetic resonance imaging. The characteristic imaging findings in this case were fetal hydrops and polyhydramnios. To our knowledge, this is the youngest reported gestational age for prenatal diagnosis of CMN and it is the second case of CMN associated with fetal hydrops detected prenatally. Copyright 2003 John Wiley & Sons, Ltd.Entities:
Mesh:
Year: 2003 PMID: 14634980 DOI: 10.1002/pd.727
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050