Palatsi R
Acta Derm Venereol. 1975;55(3):233-6.
An extreme case of Klippel-Trenaunay-Parkes Weber syndrome is presented. The patient had extensive cutaneous naevus involving the left side of the body and consisting of naevus flammeus, hemangioma cavernosum, and naevus verrucosus. The left extremities were longer and there were multiple arteriovenous connections between a and v subclavia and a and v radialis. Secondary symptoms were sciatica, varicosity and osteoporosis.
本文报告了一例Klippel-Trenaunay-Parkes Weber综合征的极端病例。患者左侧身体有广泛的皮肤痣,包括火焰状痣、海绵状血管瘤和疣状痣。左侧肢体较长,锁骨下动静脉和桡动静脉之间存在多处动静脉连接。继发症状为坐骨神经痛、静脉曲张和骨质疏松。