Djindjian M, Djindjian R, Hurth M, Rey A, Houdart R
Surg Neurol. 1977 Oct;8(4):229-37.
Five cases in which the Klippel-Trenaunay-Weber syndrome was associated with a spinal cord arteriovenous malformation are reported: they formed part of a series of 150 spinal arteriovenous malformations. Hypertrophic lesions, dilated arteries and varicose veins were present in every case, but cutaneous angiomatosis was found in only two. In each case, there was an intramedullary AVM. The relationship of the Klippel-Trenaunay-Weber syndrome to the regional angiomatous phacomatoses is discussed.
本文报告了5例Klippel-Trenaunay-Weber综合征合并脊髓动静脉畸形的病例:它们是150例脊髓动静脉畸形系列病例的一部分。每例均存在肥厚性病变、扩张的动脉和曲张的静脉,但仅2例发现皮肤血管瘤病。每例均有髓内动静脉畸形。文中讨论了Klippel-Trenaunay-Weber综合征与局部血管瘤性错构瘤病的关系。