Mediastinal (thymic) large B-cell lymphoma is a rare type of non-Hodgkin lymphoma that develops in the thymus, a small gland located behind the breastbone. This type of lymphoma usually affects people in their 20s and 30s and is more common in women than men.
Mediastinal (thymic) large B-cell lymphoma can spread to the lymph nodes of the head, face, and neck, causing swelling and pain. The lymph nodes are part of the body's immune system and help fight infections, but they can also be affected by cancer.
Symptoms of mediastinal (thymic) large B-cell lymphoma may include chest pain, coughing, difficulty breathing, fever, night sweats, and weight loss. If the lymphoma spreads to the lymph nodes of the head, face, and neck, additional symptoms may include swollen lymph nodes, pain, and difficulty swallowing or speaking.
Diagnosis of mediastinal (thymic) large B-cell lymphoma usually involves a physical exam, blood tests, imaging tests, and a biopsy of the affected tissue. A biopsy involves removing a small sample of tissue for examination under a microscope to determine if cancer cells are present.
Treatment for mediastinal (thymic) large B-cell lymphoma usually involves chemotherapy, radiation therapy, or a combination of both. In some cases, surgery may be necessary to remove the affected tissue. However, the specific treatment plan will depend on the stage of the cancer, the location of the cancer, and the overall health of the patient.
If you are experiencing symptoms of mediastinal (thymic) large B-cell lymphoma or have been diagnosed with this rare form of lymphoma, it is important to talk to your doctor about your treatment options. With early detection and treatment, many patients are able to successfully manage this rare form of cancer.
To see full information about treatment please Sign up or Log in