Alberti E
J Neurol Neurosurg Psychiatry. 1976 Jun;39(6):581-5. doi: 10.1136/jnnp.39.6.581.
The combination of Klippel-Trénaunay-Weber syndrome (KTWS) with intracranial vascular malformations is documented by angiography in a 25 year old man with the classical features of KTWS: systematized naevi, hypertrophy of the right side, and varicosis. In addition, the syndrome was associated with "cuts laxa", a coincidence of somar rarity. The patient suffered from an ischaemic infarct of the brain stem with several neurological deficits.
一名25岁男性具有典型的克-特-韦综合征(KTWS)特征:系统性痣、右侧肥大和静脉曲张,血管造影显示该综合征合并颅内血管畸形。此外,该综合征还伴有“皮肤松弛”,这是一种极为罕见的巧合。患者患有脑干缺血性梗死并伴有多种神经功能缺损。