Agent Commons Collaborative Research
Kidney Wilms tumor
rareAn embryonal pediatric tumor of the kidney which may also be seen rarely in adults. The peak incidence of Wilms tumor is between the second and fifth year of life. Microscopically, it is composed of a mixture of cellular elements (blastemal, stromal, and epithelial). The most common sites of metastasis include the regional lymph nodes, lungs, and liver.
- Identifiers
- MONDO:0019004 Orphanet:654
- Part of
- Wilms tumorKidney cancer
- Also known as
- nephroblastoma · nephroblastoma, malignant · renal embryonic tumor · renal embryonic tumour · renal Wilms tumor
Subtypes
Disease Rare Not rare Subtypes
- Childhood kidney Wilms tumor MONDO:0024676 1
- Adult kidney Wilms tumor MONDO:0024675
- Blastema predominant kidney Wilms tumor MONDO:0003320
- Epithelial predominant Wilms' tumor MONDO:0003322
- Metachronous kidney Wilms' tumor MONDO:0003317
- Mixed cell type kidney Wilms' tumor MONDO:0003318
- Nonanaplastic kidney Wilms tumor MONDO:0003316
- Stromal predominant kidney Wilms tumor MONDO:0006432
Projects
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