Wilms tumor is a rare type of kidney cancer. It causes a tumor on one or both kidneys. It usually affects children, but can happen in adults. Having certain genetic conditions or birth defects can increase the risk of getting it. Children that are at risk should be screened for Wilms tumor every three months until they turn eight.
Symptoms include a lump in the abdomen, blood in the urine, and a fever for no reason. Tests that examine the kidney and blood are used to find the tumor.
Doctors usually diagnose and remove the tumor in surgery. Other treatments include chemotherapy and radiation and biologic therapies. Biologic therapy boosts your body's own ability to fight cancer.
NIH: National Cancer Institute
- General Information about Wilms Tumor and Other Childhood Kidney Tumors (National Cancer Institute) Also in Spanish
- What Are Wilms Tumors? (American Cancer Society)
- Wilms Tumor (Nemours Foundation) Also in Spanish
- Signs and Symptoms of Wilms Tumors (American Cancer Society)
Prevention and Risk Factors
- Can Wilms Tumors Be Found Early? (American Cancer Society)
Treatments and Therapies
- Drugs Approved for Wilms Tumor and Other Childhood Kidney Cancers (National Cancer Institute)
- Nephrectomy (Kidney Removal) (Mayo Foundation for Medical Education and Research) Also in Spanish
- Treatment Option Overview (Wilms Tumor and Other Childhood Kidney Tumors) (National Cancer Institute) Also in Spanish
- ClinicalTrials.gov: Wilms Tumor (National Institutes of Health)
Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine)
- Article: Identification of the expression patterns and potential prognostic role of m6A-RNA...
- Article: Bioinformatical analysis of the key differentially expressed genes for screening potential...
- Article: CCNB1 is a novel prognostic biomarker and promotes proliferation, migration and...
- Wilms Tumor -- see more articles