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Lymphedema is a health condition involving swelling of the lymph nodes, usually in the arms or legs, due to inadequate drainage of the lymph fluid from the body.
The lymphatic system plays an essential role in the body by circulating of lymph throughout the body to collect foreign bodies such as bacteria, viruses and waste products. The waste products can be filtered out by lymphocytes that are designed to fight infection in the body.
There are primary and secondary cases of lymphedema, depending on if it was caused by another underlying health condition.
Primary lymphedema is rare and usually an inherited condition that arises as a result of abnormal development of the lymphatic system, including:
Although the pathogenesis of primary lymphedema is not entirely known, it is thought to be caused by gene mutations that affect the development of the lymphatic system. This result in a reduction of the individual’s ability to drain the lymph fluid as required.
A genetic link has been suggested due to the high prevalence of individuals with the condition that have a close relative with the condition. No specific genes are currently associated with the condition, however, and there is scarce evidence to suggest that offspring of affected individuals are at risk.
Secondary lymphedema is the most common type and occurs as a result of a condition or procedure that has caused damage to the lymphatic system.
Secondary lymphedema is particularly common among patients that have had treatment for cancer that may have damaged the lymphatic system. The symptoms of this may present shortly after the procedure or be delayed for several months or years.