Spallone A, Tcherekayev V A
Institute of Neurosurgery, Academy of Medical Sciences of Russia, Moscow.
Surg Neurol. 1996 Mar;45(3):241-4. doi: 10.1016/0090-3019(95)00378-9.
Klippel-Trenaunay syndrome is a rare neurocutaneous disorder in which skeletal hypertrophy, vascular nevi, and vessel anomalies coexist. Involvement of the cranial bone is rare, and intracranial anomalies associated with features of this syndrome are exceptional. We report a case of an adult Klippel-Trenaunay woman with a huge cranial hypertrophy harboring of the same time multiple meningiomas and a fusiform intracranial aneurysm. Although meningioma and intracranial aneurysms have been described in Klippel-Trenaunay patients, such an association has not been reported previously in patients with this syndrome.
克-特综合征是一种罕见的神经皮肤疾病，其特征为骨骼肥大、血管痣和血管异常同时存在。颅骨受累罕见，与该综合征特征相关的颅内异常情况更是罕见。我们报告一例成年克-特综合征女性患者，其颅骨巨大肥大，同时伴有多发脑膜瘤和梭形颅内动脉瘤。虽然此前已有文献报道克-特综合征患者存在脑膜瘤和颅内动脉瘤，但该综合征患者出现这种关联此前尚未见报道。
