An unusual case of Klippel-Trénaunay-Weber syndrome presenting with portosystemic encephalopathy

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Abstract

We report a unique male patient presenting with portosystemic encephalopathy (PSE) due to intrahepatic portohepatic venous (PHV) shunts. He was diagnosed as having Klippel-Trénaunay-Weber syndrome (KTWS) based on the findings of a hemitruncal port-wine stain with subcutaneous arteriovenous fistulae and varicose veins in the legs. However, limb-hypertrophy, which is one of the most cardinal manifestations of KTWS, was absent, and in KTWS, PSE is quite a rare clinical manifestation. Hence, the clinical picture of this patient was unusual. Our clinical observation suggests that KTWS can be one of the underlying disorders causing PSE. © 2008 The Japanese Society of Internal Medicine.

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Yazaki, M., Kaneko, K., Tojo, K., Miyazaki, D., Shimojima, Y., Ueda, K., & Ikeda, S. I. (2008). An unusual case of Klippel-Trénaunay-Weber syndrome presenting with portosystemic encephalopathy. Internal Medicine, 47(18), 1621–1625. https://doi.org/10.2169/internalmedicine.47.1130

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