Fukutake T, Kawamura M, Moroo I, Asahina M, Hirayama K
Department of Neurology, School of Medicine, Chiba University.
Rinsho Shinkeigaku. 1991 Mar;31(3):275-9.
We reported two patients with neurocutaneous angiomatosis. Patient 1, a 36-year-old woman of Cobb syndrome had cutaneous portwine angiomas in the high back and spinal arteriovenous malformations at the level of Th4-11. She had also atrophy and livedo reticularis presenting during standing position in the left lower extremity. Patient 2, a 47-year-old man of Klippel-Trenaunay-Weber syndrome had varices in the bilateral lower extremities, cutaneous portwine angiomas in the high back and bilateral lower extremities, and hypertrophy of the bilateral legs. Neuroradiological examination revealed abnormal vessels in the spinal canal at the level of C5 and Th4. These syndromes may have no essential difference because of the presence of neural and cutaneous angiomas at the corresponding level, venous system disorders and trophic changes (hypertrophy/atrophy).
我们报告了两名患有神经皮肤血管瘤病的患者。病例1为一名36岁患有科布综合征的女性,其背部上方有皮肤葡萄酒色血管瘤,胸4至胸11水平存在脊髓动静脉畸形。她还出现了左下肢站立时的萎缩和网状青斑。病例2为一名47岁患有克-特-韦综合征的男性,双侧下肢有静脉曲张,背部上方及双侧下肢有皮肤葡萄酒色血管瘤,且双侧腿部肥大。神经放射学检查显示颈5和胸4水平椎管内有异常血管。由于在相应水平存在神经和皮肤血管瘤、静脉系统紊乱以及营养改变(肥大/萎缩),这些综合征可能并无本质区别。