Lymfopeesi

Lymfopeesi is a rare congenital disorder characterized by the absence or severe underdevelopment of lymphatic vessels. This condition affects the body's ability to drain lymph fluid, leading to a buildup of fluid in tissues, a process known as lymphedema. Lymfopeesi can manifest in various ways, including swelling in the limbs, abdomen, or other parts of the body from birth or early childhood. The severity can range from mild to profound, impacting mobility and overall health.

The exact cause of lymfopeesi is not fully understood, but it is believed to result from genetic mutations that disrupt the normal development of the lymphatic system during fetal development. Diagnosis is typically made through clinical examination and imaging techniques such as lymphangiography or lymphoscintigraphy, which visualize the lymphatic system. Management strategies focus on reducing swelling and preventing complications. These often involve manual lymphatic drainage, compression therapy, exercise, and proper skin care to avoid infections, which can exacerbate lymphedema. While there is no cure for lymfopeesi, a multidisciplinary approach can significantly improve the quality of life for affected individuals.