The association of aniridia and wilms' tumor: Methods of surveillance and diagnosis
- 1 January 1983
- journal article
- research article
- Published by Wiley in Medical and Pediatric Oncology
- Vol. 11 (2) , 73-75
- https://doi.org/10.1002/mpo.2950110202
Abstract
The association between aniridia and Wilms' tumor (WT) is well known. The availability of data on a large number of WT patients entered on the first and second National Wilms' Tumor Studies provided the opportunity to review which examinations had been most effective in detecting the presence of WT in patients being followed with aniridia. The records of 1287 patients were available and 13 or 1% had known aniridia. The details of the prediagnostic studies were available in 9/13 patients. Those nine patients had been examined regularly by IVP at intervals of 3–12 months prior to the discovery of the WT, but in only one was the unsuspected WT detected by these means. In the remaining eight patients, the tumor was discovered by palpation in six and suspected because of hematuria in two. It is concluded that repeated IVP's are not a satisfactory method to diagnose a WT at an early stage and newer radiodiagnostic studies, such as ultrasonography, will probably prove more effective.Keywords
This publication has 10 references indexed in Scilit:
- RETROSPECTIVE VALIDATION OF A NEW STAGING SYSTEM FOR WILMS TUMOR1981
- Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13Cytogenetic and Genome Research, 1979
- Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor studyCancer, 1978
- Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial DeletionPediatrics, 1978
- Wilms' tumor in seven children withcongenital aniridiaJournal of Pediatric Surgery, 1975
- Incidence of malignant tumors in U.S. childrenThe Journal of Pediatrics, 1975
- Wilms' tumorUrology, 1974
- Wilms' Tumor and Congenital AniridiaJAMA, 1968
- Association of Wilms's Tumor with Aniridia, Hemihypertrophy and Other Congenital MalformationsNew England Journal of Medicine, 1964