| Literature DB >> 17317899 |
Zdzisław Michał Woźniak1, Krystyna Sawicz-Birkowska, Urszula Zaleska-Dorobisz, Jerzy Rabczyński, Michał Jeleń, Wojciech Apoznański.
Abstract
Congenital mesoblastic nephroma (CMN) accounts for approximately 5% of paediatric renal tumours with the highest peak of incidence during the first 3 postnatal months. CMN almost always has a favourable prognosis. Therefore, CMN needs to be correctly diagnosed and differentiated, principally histologically, from other pediatric neoplasms. We present a clinicopathologic study of 5 cases of CMN.Entities:
Mesh：
Year: 2006 PMID： 17317899
Source DB: PubMed Journal: Med Wieku Rozwoj