Childhood Tracheobronchial Tumors (PDQ®)–Patient Version

Tracheobronchial tumors are rare, abnormal growths that form in the windpipe (trachea) or the large airways in the lungs called the bronchi. These tumors can be benign, which means they are not cancer, or cancerous. Benign tumors are more common in children. If a child has a benign tumor, they may need treatment to prevent the tumor from growing and putting pressure on nearby tissue in the airway. If the tumor is cancerous, the treatment is aimed at killing the cancer cells and keeping them from spreading to other parts of the body.

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Several types of tracheobronchial tumors may affect children:

Tracheobronchial tumors in children are caused by certain changes to the way cells in the lining of the trachea or large bronchi function, especially how they grow and divide into new cells. Often, the exact cause of these cell changes is unknown. To learn more about how cancer develops, see What Is Cancer?

A risk factor is anything that increases the chance of getting a disease. There are no known risk factors for childhood tracheobronchial tumors.

Symptoms of tracheobronchial tumors are a lot like symptoms of asthma, which can make it hard to diagnose the tumor. It's important to check with your child's doctor if your child has any symptoms such as:

These symptoms may be caused by problems other than a tracheobronchial tumor. The only way to know is to see your child's doctor.

If your child has symptoms that suggest a tracheobronchial tumor, their doctor will need to find out if these are due to cancer or to another problem. The doctor will ask when the symptoms started and how often your child has been having them. They will also ask about your child's personal and family medical history and do a physical exam. Depending on these results, they may recommend other tests. If your child is diagnosed with a tracheobronchial tumor, the results of these tests will help you and your child's doctor plan treatment.

The tests used to diagnose tracheobronchial tumors in children may include:

CT scan (CAT scan)

A CT scan uses a computer linked to an x-ray machine to make a series of detailed pictures of areas inside the body, such as the neck and chest. The pictures are taken from different angles and are used to create 3-D views of tissues and organs. A dye may be injected into a vein or swallowed to help the organs or tissues show up more clearly. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography. To learn more, see Computed Tomography (CT) Scans and Cancer.

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You may want to get a second opinion to confirm your child’s diagnosis and treatment plan. If you seek a second opinion, you will need to get medical test results and reports from the first doctor to share with the second doctor. The second doctor will review the pathology report, slides, and scans. They may agree with the first doctor, suggest changes to the treatment plan, or provide more information about your child’s tumor.

To learn more about choosing a doctor and getting a second opinion, see Finding Cancer Care. You can contact NCI’s Cancer Information Service via chat, email, or phone (both in English and Spanish) for help finding a doctor, hospital, or getting a second opinion. For questions you might want to ask at your child's appointments, see Questions to Ask Your Doctor about Cancer.

A pediatric oncologist, a doctor who specializes in treating children with cancer, oversees treatment of tracheobronchial tumors. The pediatric oncologist works with other health care providers who are experts in treating children with cancer and who specialize in certain areas of medicine. Other specialists may include:

There are different types of treatment for children and adolescents with tracheobronchial tumors. You and your child’s care team will work together to decide treatment. Many factors will be considered, such as your child’s overall health and whether the tumor is newly diagnosed or has come back after treatment.

Your child’s treatment plan will include information about the tumor, the goals of treatment, treatment options, and the possible side effects. It will be helpful to talk with your child’s care team before treatment begins about what to expect. For help every step of the way, see our booklet, Children with Cancer: A Guide for Parents.

For all tracheobroncial tumors except rhabdomyosarcoma, treatment might include surgery to remove the tumor. The lymph nodes and vessels where cancer has spread are also removed. Sometimes a surgery called a sleeve resection is done.

For rhabdomyosarcoma in the trachea or bronchi, treatment might include chemotherapy and radiation therapy:

To learn more about rhabdomyosarcoma and its treatment, see Childhood Rhabdomyosarcoma Treatment.

For inflammatory myofibroblastic tumors in the trachea or bronchi, in addition to surgery, treatment may include targeted therapy. Targeted therapy uses drugs or other substances to identify and attack specific cancer cells. Crizotinib may be used if the tumor has a certain change in the ALK gene. Learn more about Targeted Therapy to Treat Cancer.

If the cancer comes back after treatment, your child's doctor will talk with you about what to expect and possible next steps. There might be treatment options that may shrink the cancer or control its growth. If there are no treatments, your child can receive care to control symptoms from cancer so they can be as comfortable as possible.

Joining a clinical trial may be an option. There are different types of clinical trials for childhood cancer. For example, a treatment trial tests new treatments or new ways of using existing treatments. Supportive care and palliative care trials look at ways to improve quality of life, especially for those who have side effects from cancer and its treatment.

You can use the clinical trial search to find NCI-supported cancer clinical trials that are accepting patients. The search allows you to filter trials based on the type of cancer, your child's age, and where the trials are being done.

To learn more, see Clinical Trials Information for Patients and Caregivers. 

If your child has been diagnosed with a tracheobronchial tumor, you likely have questions about how serious the cancer is and about your child's chances of survival. The likely outcome or course of a disease is called prognosis.

The prognosis depends on many factors, including:

The prognosis for children with tracheobronchial tumors that can be removed by surgery is very good. This is the case for most tracheobronchial tumors except rhabdomyosarcoma, which requires more aggressive treatment.

No two people are alike, and responses to treatment can vary greatly. Your child's cancer care team is in the best position to talk with you about your child's prognosis.

Cancer treatments can cause side effects. Which side effects your child might have depends on the type of treatment they receive, the dose, and how their body reacts. Talk with your child's treatment team about which side effects to look for and ways to manage them.

To learn more about side effects that begin during treatment for cancer, visit Side Effects.

Problems from cancer treatment that begin 6 months or later after treatment and continue for months or years are called late effects. Late effects of cancer treatment may include:

Some late effects may be treated or controlled. It is important to talk with your child's doctors about the possible late effects caused by some treatments.

As your child goes through treatment, they will have follow-up tests or check-ups. Some of the tests that were done to diagnose the cancer may be repeated to see how well the treatment is working. Decisions about whether to continue, change, or stop treatment may be based on the results of these tests.

Some of the tests will continue to be done from time to time after treatment has ended. The results of these tests can show if your child's condition has changed or if the cancer has recurred (come back).

When your child has a tumor, every member of the family needs support. Taking care of yourself during this difficult time is important. Reach out to your child’s treatment team and to people in your family and community for support. To learn more, see Support for Families When a Child Has Cancer and the booklet Children with Cancer: A Guide for Parents.

For more childhood cancer information and other general cancer resources, see: