Abstract
Klippel-Trenaunay syndrome (KTS) is characterized by the classic triad of capillary malformations manifesting as a "port-wine stain", venous varicosities, and bone and/or soft tissue hypertrophy. Imaging could help to diagnose and evaluation of KTS. Case Presentation: We report a 12-year-old with progressive enlargement of the right lower limb with geographic stain and venous varicosities. The patient also underwent MRI and angiography, which revealed multiple nidus with multiple feeding arteries. Conclusion: Klippel-Trenaunay Syndrome is a rare condtion. MRI and Arteriography could help diagnose KTS for confirmation, monitoring progression, or identification of complications.
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