Lymphangiomatosis: Difference between revisions

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Revision as of 00:40, 17 March 2025

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

The symptoms of lymphangiomatosis vary depending on the organs affected. Common symptoms include:

Causes

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

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

There is currently no cure for lymphangiomatosis. Treatment is aimed at managing symptoms and improving quality of life. This may include:

Prognosis

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

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