Rhabdomyosarcoma is a type of cancer. It starts in cells that grow into skeletal muscle cells. These cells are called rhabdomyoblasts. Skeletal muscles are the muscles that control to move the body.
This cancer is most common in children under age 10, but it' s rare. It can form in muscles anywhere in the body. A skull base rhabdomyosarcoma forms in the head and neck. It can start in the area where the spine connects to the skull (skull base). It can also grow in other parts of the head, like the eyes, nose, throat, or sinuses.
There are two main types of rhabdomyosarcoma:
Embryonal. This is the most common type. It’s the most likely type to affect the base of the skull.
Alveolar. This type is more common in older children and teens. It’s more likely to affect the trunk, arms, or legs. It grows more quickly. It’s more likely to spread to other areas of the body (metastasize).
The exact cause of this cancer is not known. Changes in the genetic material in cells (DNA) likely cause the normal cells to turn into cancer.
Some health conditions that are passed down through families (genetic) increase a child's risk. These include:
Neurofibromatosis type 1 (NF1)
Symptoms depend on the location and the size and of the tumor. They can include:
Problems with the sense of smell
Trouble with eye movement
Bulging of the eye
Numbness or weakness of the face
Trouble hearing, ringing in the ears (tinnitus), ear pain, or dizziness
Symptoms that rhabdomyosarcoma has spread may include:
A lump or swelling in the neck
The symptoms can be like other health conditions. Make sure your child sees a healthcare provider for a diagnosis.
Your child's healthcare provider will ask about your child's health history and symptoms. A physical exam will be done and will include a neurological exam. The exam tests reflexes, muscle strength, eye and mouth movement, and coordination. Your child's healthcare provider may refer your child to a cancer specialist (oncologist). Your child may need other tests such as:
CT scan.A CT scan uses a series of X-rays and a computer to make detailed pictures of the inside of the body. Your child may drink contrast dye or it may be injected into your child's vein. The contrast helps show more details.
MRI.An MRI uses large magnets, radio waves, and a computer to make detailed pictures of the inside of the body. Contrast dye may be injected into your child's vein. It helps show details clearly.
Lumbar puncture. A needle is placed into the spinal canal in the lower back. This is the area around the spinal cord. A small sample of cerebrospinal fluid (CSF) is removed. CSF is the fluid around the brain and spinal cord. The sample is checked for cancer cells.
Biopsy.Tumor cells are removed and sent to a lab for testing. This is done to find out the type of tumor and how quickly it’s likely to grow. This may be done during \ surgery.
After a diagnosis has been made, the cancer is staged. Staging is the process of finding out where the cancer is, how big it is, seeing if the cancer has spread (metastasized), and where it has spread. Staging also helps to decide on the best treatment options. There are different ways of staging cancer, but most range from stage 1 to stage 4, where a stage 4 is cancer that has spread to other parts of the body. Talk with your child's healthcare provider about the stage of your child's cancer and what it means.
If your child has been diagnosed with skull base rhabdomyosarcoma, you may want your child to see another oncologist to get a second opinion. This may help you better understand the treatment options and feel good about the treatment choices you make.
Because the cancer is so rare, it's important for your child to be treated at a center that specializes in treating cancer in children . Most children are treated in a clinical trial. These are studies that compare the best treatments available now with treatments that are thought to be even better. Your doctor may talk to you about this option.
Treatment will depend on the location, stage, and other factors. The cancer can be treated with any of these:
Surgery.The goal of surgery is to remove all of the tumor. The doctors will try to keep your child's body working and looking as normal as possible. A surgeon who specializes in the body area of tumor growth may be needed. This may be a head and face (craniofacial) surgeon, or an ear, nose, and throat (otolaryngologist) doctor. It may be a brain surgeon (neurosurgeon). Or it may be another type of doctor.
Chemotherapy (chemo). These are medicines that kill cancer cells. Chemo is almost always used to treat rhabdomyosarcoma. It's given through a tube (IV) that's put to a vein in the arm or chest.
Radiation therapy. These are high-energy X-rays or other types of radiation used to kill cancer cells or stop them from growing. It may be used when a tumor is hard to remove with surgery. Radiation therapy is usually given along with chemotherapy.
Clinical trials. Ask your child's healthcare provider if there are any treatments being tested that may work well for your child. Many new treatments are only available in clinical trials.
Supportive care.Treatment can cause side effects. Medicines and other treatments can be used for pain, fever, infection, and nausea and vomiting. This a key part of cancer care.
With any cancer, how well a child is expected to recover (prognosis) varies. Keep in mind:
Getting medical treatment right away is important for the best prognosis. Cancer that has spread is harder to treat.
Ongoing follow-up care after treatment is needed.
Talk with the doctor about any concerns you have or problems you notice. Your child's treatment team wants to know as much as they can about how your child is doing.
A child may have short- and long-term problems from the tumor or from treatment. They may include things like:
Damage to the brain or nervous system that causes problems with coordination, muscle strength, speech, or eyesight
Problems after surgery, such as infection, bleeding, and problems with general anesthesia
Infection and bleeding from chemotherapy
Delayed growth and development
Problems with reproduction (infertility)
Return of the cancer (recurrence)
Increased risk of other cancers later in life
Talk with the doctor about what you should watch for and what can be done to help prevent complications.
A child with skull base rhabdomyosarcoma needs special care for the rest of his or her life. Your child will be seen by oncologists and other healthcare providers to treat any late effects of treatment and to watch for signs or symptoms of the tumor returning. Your child will be checked with imaging tests and other tests. And your child may see other healthcare providers for problems from the tumor or from treatment. For example, your child may see an eye doctor (ophthalmologist) for vision problems.
Your child may need therapy to help with movement and muscle strength. This may be done by physical and occupational therapists. If your child's speech is affected, he or she may need help from a speech therapist. Your child may also need the help of other therapists for learning or emotional problems.
You can help your child manage his or her treatment in many ways. For example:
Your child may have trouble eating. A dietitian may be able to help.
Your child may be very tired. He or she will need to balance rest and activity. Encourage your child to get some exercise. This is good for overall health. And it may help to lessen tiredness.
Get emotional support for your child. Find a counselor or child support group can help.
Make sure your child attends all follow-up appointments.
Call the healthcare provider if your child has:
Symptoms that get worse
Side effects from treatment
A skull base rhabdomyosarcoma is cancer that forms in the head and neck.
Symptoms include problems with the sense of smell, eye sight, hearing, swallowing, and facial weakness.
Treatment includes surgery, chemotherapy, and radiation therapy.
Because the cancer is so rare, it's important for your child to be treated at a center that specializes in the disease.
Tips to help you get the most from a visit to your child’s healthcare provider:
Know the reason for the visit and what you want to happen.
Before your visit, write down questions you want answered.
At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you for your child.
Know why a new medicine or treatment is prescribed and how it will help your child. Also know what the side effects are.
Ask if your child’s condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if your child does not take the medicine or have the test or procedure.
If your child has a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your child’s provider after office hours. This is important if your child becomes ill and you have questions or need advice.