Cancer is rare in teens. Certain diseases like breast cancer usually affect adult women — teen girls are unlikely to get this form of cancer. But some types are more likely to occur in teens. Testicular cancer, for example, tends to affect younger guys rather than older men.
The types of cancers teens get have one thing in common: cells growing in an uncontrolled way. Cells are the basic components or "building blocks" of the human body. Cancer occurs when cells develop abnormally and grow in an uncontrolled way. Read on to learn more about some types of cancer that teens may get, including warning signs and symptoms and how these cancers can be treated.
Osteosarcoma (pronounced: os-tee-oh-sahr-KOH-muh) is the most common type of bone cancer. In teens, it can sometimes appear during their growth spurts and tends to show up in people who are taller than average. In most cases, there is no known cause for osteosarcoma.
The most common symptoms of osteosarcoma are pain and swelling in an arm or leg that is sometimes accompanied by a lump. Some people have more pain at night or when they exercise. Osteosarcoma is most often found in the bones around the knee but can occur in other bones as well. In some cases, a tumor can spread or metastasize (when cells from a tumor break away from the original cancer site and travel to a different tissue or organ) to the lungs and other bones.
Treatment for osteosarcoma usually involves chemotherapy (medication that kills cancer cells) as well as surgery to remove the tumor. A doctor may perform limb-salvage surgery, where the bone that has cancer is removed and the limb (usually an arm or leg) is saved from amputation by filling the gap with a bone graft or special metal rod. In other cases, a doctor may need to amputate (remove) part or all of the limb to fight the cancer.
Losing a limb can be devastating, especially for teens who are already dealing with body changes. Counseling and physical therapy (or physical rehabilitation) can both be helpful in this situation. People who have amputations are usually fitted with a prosthesis (pronounced: pros-THEE-sis), or artificial limb. Most teens with a prosthesis are able to return to normal activities, even sports.
Most people develop side effects, such as hair loss, bleeding, infections, and heart or skin problems, from medicines used in chemotherapy treatment for osteosarcoma. Chemotherapy may also increase the person's risk of developing other cancers in the future. The good news is that most teens with osteosarcoma do recover.
Another type of cancer that affects the bone is Ewing's sarcoma. It is similar to osteosarcoma in that it also affects teens and young adults and is usually located in bone.
Most teens with Ewing's sarcoma receive chemotherapy as well as surgery. Some patients will also need radiation in addition to or instead of surgery to make sure that remaining cancer cells have been destroyed. Ewing's sarcoma generally responds well to chemotherapy and radiation.
Osteosarcoma and Ewing's sarcoma share common risk factors and side effects from treatment. Chances for recovery depend upon where the tumor is located, its size, and whether it has spread. But both types of bone cancer respond well to treatment and are curable in many cases.
Leukemia is one of the most common childhood cancers. It occurs when large numbers of abnormal white blood cells called leukemic blasts fill the bone marrow and sometimes enter the bloodstream.
Because these abnormal blood cells are defective, they don't help protect the body against infection the way normal white blood cells do. And because they grow uncontrollably, they take over the bone marrow and interfere with the body's production of other important types of cells in the bloodstream, like red blood cells (which carry oxygen) and platelets (which help blood to clot).
Leukemia causes problems like bleeding, anemia (low numbers of red blood cells), bone pain, and infections. It can also spread to other places like the lymph nodes, liver, spleen, brain, and the testicles in males.
The types of leukemia most likely to occur in teens are acute lymphocytic (pronounced: lim-fuh-SIT-ik) leukemia (ALL) and acute myelogenous (pronounced: my-uh-LAHG-uh-nus) leukemia (AML).
Virtually all people with ALL and AML are treated with chemotherapy, and some also receive stem cell transplants, in which they are given new stem cells from another person. Bone marrow transplants are a common form of stem cell transplantation. Some people also receive radiation. The length of treatment and types of medicine given will vary depending on the type of leukemia.
The chances for a cure are very good with certain kinds of leukemia. With treatment, most patients with ALL and many patients with AML are free of the disease without recurrence.
Brain tumors can also occur in teens.
Two of the most common forms are astrocytomas (pronounced: as-truh-sye-TOE-muhz) and ependymomas (pronounced: eh-pen-duh-MOE-muhz). Astrocytomas are tumors of the brain that originate from cells in the brain called astrocytes. This type of tumor doesn't usually spread outside the brain and spinal cord and doesn't usually affect other organs.
Ependymomas are tumors that usually begin in the lining of brain ventricles. The brain has four ventricles, or cavities, that are a pathway for cerebrospinal fluid, a liquid substance that cushions the brain and spine and protects them from trauma.
No one knows the exact cause of primary brain cancer. One possibility is that as the brain and spinal cord were forming, a problem with the cells occurred.
Treatments vary depending upon the type and location of the tumor. If it is possible to remove a tumor, surgery is usually performed, followed by radiation. Some patients receive chemotherapy as well.
The chance of surviving a brain tumor depends on its type, location, and treatment. But there is a very good chance that if the tumor can be removed and additional treatment is given, the cancer can be cured.
Lymphoma refers to cancer that develops in the lymphatic system, which includes the lymph nodes, thymus, spleen, adenoids, tonsils, and bone marrow. The lymph system functions in the body by fighting off germs that cause infection and illness. Most teens with lymphoma have either Hodgkin's lymphoma or non-Hodgkin's lymphoma.
Hodgkin's lymphoma usually occurs in adolescents and young adults. It can show up in lymph nodes in the neck, armpits, chest, or other places. The lymph nodes become enlarged but are usually not painful. Hodgkin's disease is identified by large, unusual cells called Reed-Sternberg cells that are detected under a microscope after a biopsy, a procedure in which a doctor removes a small tissue sample to examine it for cancer cells. Chemotherapy and often radiation are used to treat Hodgkin's disease.
Non-Hodgkin's lymphoma (NHL) is similar to leukemia (ALL) because both involve malignant lymphocytes (pronounced: LIM-fuh-sytes), white blood cells found in lymph nodes, and because many of the symptoms of these diseases are the same. NHL is usually treated with chemotherapy.
Teens with Hodgkin's lymphoma or NHL who have completed their treatment have an excellent chance for cure.
Other cancers that teens may get — although they are generally rare — include testicular cancer and rhabdomyosarcomas.
Although testicular cancer is actually rare in teen guys, overall it is the most common cancer in males ages 15 to 35. Testicular cancer is almost always curable if it is caught and treated early. Guys should learn how to examine their testicles regularly to detect any abnormal lumps or bumps, which are usually the earliest sign of testicular cancer.
Rhabdomyosarcomas (pronounced: rab-doe-my-uh-sahr-KOE-muhz), or soft tissue sarcomas, are less common cancers that mostly occur in infants, kids, and teens. With these cancers, cancer cells grow in the soft tissues of the muscles (the body's muscles that a person controls for movement). Though these cancers can occur anywhere in the body, rhabdomyosarcomas most frequently happen within the muscles in the trunk, arms, or legs. The types of treatment used and chances for recovery depend upon where the rhabdomyosarcoma is located and whether the cancer has spread to other areas of the body.
Reviewed by: Robin Miller, MD
Date reviewed: February 2014