Mesoblastic nephromas: a study of 29 tumours from the SIOP nephroblastoma file
- 1 July 1985
- journal article
- research article
- Published by Wiley in Histopathology
- Vol. 9 (7) , 741-750
- https://doi.org/10.1111/j.1365-2559.1985.tb02860.x
Abstract
In a series of 889 Wilms' tumours we found 29 pure mesoblastic nephromas. The age of the patients varied from newborn to 22 months, but only five were older than four months. Two histologic types were recognized—leiomyomatous (9) and cellular (20) with a fibrohistiocytic appearance. The leiomyomatous type was almost invariably in stage I, smaller and present in younger infants. At operation half of the cellular type has ruptured or infiltrated the renal pelvis or perirenal tissue. Two patients died of postoperative complications. All others are alive after four years and free from disease.Keywords
This publication has 16 references indexed in Scilit:
- Therapy and outcome in 51 children with mesoblastic nephroma: A report of the national Wilms' tumor studyJournal of Pediatric Surgery, 1982
- Mesenchymal renal tumors in infancy: A reappraisalHuman Pathology, 1981
- Malignant mesenchymal nephroma of infancyThe American Journal of Surgical Pathology, 1980
- Lymph node invasion and prognosis in nephroblastomaCancer, 1980
- Leiomyomatous tumors of the infant kidneyThe Journal of Pediatrics, 1976
- Mesenchymal renal neoplasms of infancy revisitedJournal of Pediatric Surgery, 1974
- Congenital Mesoblastic Nephroma of Infancy: Report of a Case with Unusual Clinical BehaviorAmerican Journal of Clinical Pathology, 1973
- Congenital Mesoblastic Nephroma (Leiomyomatous Hamartoma): First Adult CaseJournal of Urology, 1973
- Mesenchymal renal neoplasms of infancyJournal of Pediatric Surgery, 1970
- Fetal Hamartoma of Kidney: A Benign, Symptomatic, Congenital Tumor, Not a Form of Wilms’ TumorAmerican Journal of Clinical Pathology, 1969