Malignant Rhabdoid Tumor | Diagnosis & Treatment

How are malignant rhabdoid tumors diagnosed?

Diagnostic procedures for a malignant rhabdoid tumor are used to determine the exact type of tumor your child has and whether or not the tumor has spread. Your child’s doctor will perform a complete medical and physical examination.

Your child’s physician may also order some of the following diagnostic tests:

If a biopsy is taken, the sample will be tested for mutations in a gene called SMARCB1 (this gene also goes by the names INI1SNF5, and BAF47), which is turned off in nearly all rhabdoid tumors.

If a mutation is found, your child's doctor may recommend additional tests.

What are the treatment options for a malignant rhabdoid tumor?

Treatment involves a combination of therapies including surgery, radiation, and chemotherapy. However, because this tumor is rare and aggressive, there is no defined standard of care, and treatment options may be tailored to your child's situation. Your child's doctor and other members of your care team will discuss the options with you in depth. Prompt medical attention and aggressive therapy are important for the best prognosis.


In most cases, the first step in treating malignant rhabdoid tumor is surgery. Often a surgeon will try to remove the whole tumor at the time of biopsy. Depending on the size and location of the tumor, the surgeon may remove only part of the kidney or the whole kidney.


After surgery, children with a malignant rhabdoid tumor are treated with a very aggressive course of chemotherapy, a group of drugs that interfere with the cancer cell’s ability to grow or reproduce. Different groups of chemotherapy drugs work in varied ways to fight cancer cells and shrink tumors. Often, a combination of chemotherapy drugs is used. Certain chemotherapy drugs may be given in a specific order depending on the type of cancer it is being used to treat.

Radiation therapy 

Children who are more than six months old also may receive radiation therapy as part of their treatment.

Stem cell transplantation 

The treatment of a malignant rhabdoid tumor can be so intense as to affect the body's ability to produce normal blood and immune cells. For that reason, your child's doctor may recommend that your child undergo a stem cell transplant. This involves temporarily removing some of a child’s healthy blood cells and giving her very high doses of chemotherapy and, in some cases, radiation therapy to overwhelm and destroy the malignant rhabdoid tumor. The child is then given back their own stored healthy blood cells to promote normal body and organ function once treatment is done.

Supportive care

Supportive care is treatment to prevent and treat infections, side effects of treatments, and complications. The goal is to keep your child comfortable during treatment. It also is an important part of preventing short and long-term complications of the disease and treatment.

What is the long-term outlook for children with a malignant rhabdoid tumor?

Your child’s chance of recovery and treatment options depend on a number of different factors:

  • extent of the disease
  • size and location of the tumor
  • tumor's characteristics when examined under a microscope
  • presence or absence of metastasis
  • tumor's response to therapy
  • age and overall health
  • your child's tolerance of specific medications, procedures, or therapies
  • new developments in treatment

In general, malignant rhabdoid tumors are very aggressive and difficult to treat. Patients often initially respond well to treatment, but relapse either during or shortly after treatment remains a risk. Children with germline mutations to SMARCB1 also have a high risk of developing second tumors. Prompt medical attention and appropriate therapy are important for the best prognosis.