Lymphangiomatosis
Lymphangiomatosis is a rare, non-malignant disease characterized by the abnormal growth of lymph vessels. It can affect multiple organs in the body, including the lungs, liver, spleen, and bones. The disease is most commonly diagnosed in children and young adults, but it can occur at any age.
Symptoms[edit | edit source]
The symptoms of lymphangiomatosis vary depending on the organs affected. Common symptoms include:
Causes[edit | edit source]
The exact cause of lymphangiomatosis is unknown. It is thought to be a result of a developmental error in the formation of the lymphatic system.
Diagnosis[edit | edit source]
Diagnosis of lymphangiomatosis is often challenging due to the rarity of the disease and the variability of symptoms. It typically involves a combination of medical history, physical examination, imaging studies such as CT scan or MRI, and sometimes tissue biopsy.
Treatment[edit | edit source]
There is currently no cure for lymphangiomatosis. Treatment is aimed at managing symptoms and improving quality of life. This may include:
- Pain management
- Physical therapy
- Surgery to remove or reduce the size of the abnormal lymph vessels
- Radiation therapy
- Chemotherapy
Prognosis[edit | edit source]
The prognosis for individuals with lymphangiomatosis varies widely. Some individuals may live a normal lifespan with few symptoms, while others may experience severe complications and reduced life expectancy.
See also[edit | edit source]
Lymphangiomatosis Resources | ||
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Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD