: Human diseases: Klippel-Trenaunay angiodysplasia

disease > congenital disease > malformation > Klippel-Trenaunay angiodysplasia

disease > skin appendages disease > skin disease > Klippel-Trenaunay angiodysplasia

disease > diseases of the osteoarticular system > Klippel-Trenaunay angiodysplasia

disease > tumor > benign neoplasm > angioma > Klippel-Trenaunay angiodysplasia

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Klippel-Trenaunay angiodysplasia

Klippel–Trénaunay syndrome formerly Klippel–Trénaunay–Weber syndrome and sometimes angioosteohypertrophy syndrome and hemangiectatic hypertrophy, is a rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb. It is similar to, though distinctly separate from, the less common Parkes-Weber syndrome. The classical triad of Klippel-Trenaunay syndrome consists of: vascular malformations of the capillary, venous and lymphatic vessels; varicosities of unusual distribution, particularly the lateral venous anomaly; and unilateral soft and skeletal tissue hypertrophy, usually the lower extremity. (Wikipedia)

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