Also called nephroblastoma. Kidney cancer occurring mostly in children. Also see Cancer Wilms' Tumor, and Rhabdoid Tumor.Encyclopedia Entry for Wilms Tumor :Wilms tumor. WT is the most common form of childhood kidney cancer. The exact cause of this tumor in most children is unknown. A missing iris of the eye (aniridia) is a birth defect that is sometimes associated with WT. Other birth defects linked to this type of kidney cancer include certain urinary tract problems and swelling of one side of the body, a condition called hemihypertrophy. It is more common among some siblings and twins, which suggests a possible genetic cause. The disease occurs most often in children about 3 years old. More than 90% of cases are diagnosed before 10 years of age. In rare cases, it is seen in children older than 15 years of age, and in adults.Symptoms may include any of the following: Abdominal pain Abnormal urine color Constipation Fever General discomfort or uneasiness ( malaise ) High blood pressure Increased growth on only one side of the body Loss of appetite Nausea and vomiting Swelling in the abdomen ( abdominal hernia or mass ) Sweating (at night) Blood in urine (hematuria).The health care provider will perform a physical exam and ask questions about your child's symptoms and medical history. You will be asked if you have a family history of cancer. A physical examination may show an abdominal mass. High blood pressure may also be present. Tests include: Abdominal ultrasound Abdominal x-ray BUN Chest x-ray or CT scan Complete blood count (CBC), may show anemia Creatinine Creatinine clearance CT scan of the abdomen with contrast MRI Intravenous pyelogram MR angiography (MRA) Urinalysis Alkaline phosphate Calcium Transaminases (liver enzymes) Other tests needed to determine if the tumor has spread may include: Echocardiogram Lung scan PET scan Biopsy.If your child is diagnosed with WT, do not prod or push on the child's belly area. Use care during bathing and handling to avoid injury to the tumor site. The first step in treatment is to stage the tumor. Staging helps the provider determine how far the cancer has spread and to plan for the best treatment. Surgery to remove the tumor is planned as soon as possible. Surrounding tissues and organs may also need to be removed if the tumor has spread. Radiation therapy and chemotherapy will often be started after surgery, depending on the stage of the tumor. Chemotherapy given before the surgery is also effective in preventing complications.Children whose tumor has not spread have a 90% cure rate with appropriate treatment. Prognosis is also better in children younger than 2 years of age.The tumor may become quite large, but usually remains self-enclosed. Spread of the tumor to the lungs, lymph nodes, liver, bone, or brain is the most worrisome complication. High blood pressure and kidney damage may occur as the result of the tumor or its treatment. Removal of WT from both kidneys may affect kidney function. Other possible complications of the long-term treatment of WT may include: Heart failure Secondary cancer elsewhere in the body that develops after the treatment of first cancer Short height.Call your child's provider if: You discover a lump in your child's abdomen, blood in the urine, or other symptoms of WT. Your child is being treated for this condition and symptoms get worse or new symptoms develop, mainly cough, chest pain, weight loss, or persistent fevers.For children with a known high risk for WT, screening using ultrasound of the kidneys or prenatal genetic analysis may be suggested.Nephroblastoma; Kidney tumor - Wilms.Kidney anatomy Kidney anatomy Wilms tumor Wilms tumor.Babaian KN, Delacroix SE, Wood CG, Jonasch E. Kidney cancer.