Wilms tumor (WT), a sporadic and familial childhood kidney tumor, is genetically heterogeneous. One WT gene, WT1 at 11p13, has been cloned, but only a minority of WTs carry detectable mutations at that locus. WT1 can also be excluded as the predisposition gene in most WT families, implying the exist
Primary ovarian wilms' tumor
โ Scribed by Aysegul Sahin; Jo Ann Benda
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 511 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
A case of extrarenal Wilms' tumor presenting as an ovarian mass in a woman 56 years of age is described. Histologically, glomeruloid and tubular structures were identified within nests of undifferentiated epithelium. No teratomatous components were encountered. A review of the literature found three other reports of Wilrns' tumor occurring in the female genital tract. This case represents the oldest patient with extrarenal Wilms' tumor in the literature.
๐ SIMILAR VOLUMES
## Abstract Wilms tumor (WT), an embryonic tumor arising from undifferentiated renal mesenchyme, has been a productive model for understanding the role of genes in both tumorigenesis and normal organogenesis. Approximately 2% of WT patients have a family history of WT, and even sporadic WT is thoug
A 17-month-old black male, who had bilateral Wilms tumor diagnosed nine months earlier, was presented for consideration of further therapy. He was first seen when eight months of age because of a right-sided abdominal mass. There was no hematuria and his blood pressure was normal at that time. The
Background. Intraspinal Wilms' tumor metastasis is rare, and is associated with a high mortality rate. Methods. The authors reviewed the clinical course of two patients with Wilms' tumor in whom extradural metastasis developed. In addition, a review of the literature and of patients entered in the