The first step in treating your child is forming an accurate and complete diagnosis. Your child’s physician may order a number of different tests to determine if your child has cancer and its specific type and location. These include:
- urine tests
imaging scans, including x-rays, magnetic resonance imaging (MRI), computerized tomography scan (also called a CT or CAT scan), positron emission tomography (also called a PET scan) and bone scans to produce detailed images of the inside of the body
- bone marrow biopsy/aspiration - a procedure that involves a small amount of bone marrow fluid and tissue to be taken, usually from part of the hip bones, to further examine the number, size, and maturity of blood cells and/or abnormal cells
- lymph node biopsy - a sample of tissue is removed from a lymph node and examined under a microscope
- tumor biopsy or tissue sample from the tumor to provide definitive information about the type of tumor; this is collected during surgery
lumbar puncture (spinal tap) to remove a small sample of cerebrospinal fluid (CSF) and determine if any tumor cells have started to spread. In young children, this procedure is safely performed under sedation.
- chromosome analysis – samples of blood and bone marrow can be sent to a special laboratory to look for certain changes in the chromosomes of the cancer cells
After we complete all necessary tests, our experts meet to review and discuss what they have learned about your child's condition. Then we will meet with you and your family to discuss the results and outline the best treatment options.
|Questions about your visit? Check out our Cancer and Blood Disorders Care Center for directions, contact information and other important information|