New look at mesoblastic nephroma.
Open Access
- 1 May 1986
- journal article
- research article
- Published by BMJ in Journal of Clinical Pathology
- Vol. 39 (5) , 508-513
- https://doi.org/10.1136/jcp.39.5.508
Abstract
Thirty eight mesoblastic nephromas were studied. The age range of the patients was between the neonatal period and 18 months. The presence of cartilage is consistent with a mesoblastic origin, but squamous epithelium was a feature in three tumours. Particular attention was given to the adjacent renal tissue in which various histological features were noted: vacuolated and dysplastic tubules; cysts; and subcapsular epithelial tumourlets. The findings had aspects in common with both dysplastic kidneys and nephroblastoma. Classification of the tumours as normocellular and hypercellular was attempted, but there was considerable overlap. The behaviour of the tumour was good in all cases, although follow up was relatively short on some patients, and deaths from non-neoplastic causes occurred.This publication has 12 references indexed in Scilit:
- Mesoblastic nephromas: a study of 29 tumours from the SIOP nephroblastoma fileHistopathology, 1985
- Mesoblastic nephroma contains fibronectin but lacks laminin.Journal of Clinical Pathology, 1985
- Clear cell sarcoma of the kidney with emphasis on ultrastructural studiesCancer, 1984
- Congenital mesoblastic nephroma presenting with primary reninismThe Journal of Pediatrics, 1979
- CONGENITAL AND INFANTILE NEOPLASIA OF THE KIDNEYThe Lancet, 1974
- A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal diseaseThe Journal of Pediatrics, 1970
- Fetal Hamartoma of Kidney: A Benign, Symptomatic, Congenital Tumor, Not a Form of Wilms’ TumorAmerican Journal of Clinical Pathology, 1969
- Renal tumors in the neonatal periodCancer, 1968
- CONGENITAL MESOBLASTIC NEPHROMA OF INFANCY - A REPORT OF 8 CASES AND RELATIONSHIP TO WILMS TUMOR1967