1 The Pathology Laboratories of the Children's Hospital of Akron and the Children's Hospital of Michigan, and the Department of Pathology and Division of Pediatric Surgery, Western Reserve University, Cleveland
A congenital mesoblastic nephroma occurring in eight infants is described. This tumor is composed primarily of fibroblastic tissue, and malignant epithelial components are missing. Foci of cystic and/or dysplastic tubules are always present. The tumor is thought to be histogenetically related to Wilms' tumor. Survival seems to be excellent following nephrectomy alone.
Submitted on January 27, 1967
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