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| Klippel–Trénaunay–Weber syndrome ： ウィキペディア英語版 |
Klippel–Trénaunay syndrome
Klippel–Trénaunay syndrome (KTS or KT), formerly Klippel–Trénaunay–Weber syndrome〔http://www.sturge-weber.org/resources/about-sws/conditions/17-klippel-trenaunay-syndrome.html〕 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.
==Classification==
There is disagreement as to how cases of KTS should be classified if there is an arteriovenous fistula present. Although several authorities have suggested that the term Parkes Weber syndrome is applied in those cases, ICD-10 currently uses the term "Klippel–Trénaunay–Weber syndrome".
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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