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Cerebral and spinal cavernomas associated with Klippel-Trenaunay syndrome: case report and literature review

机译:与Klippel-Trenaunay综合征相关的脑和脊髓脊髓瘤:案例报告和文献综述

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摘要

Abstract Klippel-Trenaunay-Weber syndrome (KTWS) involves a triad of conditions, including cutaneous hemangiomas, venous varicosities, and osseous and soft-tissue hypertrophy of the affected limb. We describe a rare case of multiple cavernomas in the central nervous system in a patient with KTWS. A-64-year-old man with KTWS and a previous brain hemorrhage presented with sudden onset of gait and vesicorectal disturbance. The magnetic resonance imaging scan showed a cavernoma associated with hemorrhage in his lumbosacral spinal cord. Moreover, numerous cavernomas were identified in his brain. He was treated conservatively with no adverse events. Gait disturbance improved, but vesicorectal disturbance did not improve.
机译:摘要Klippel-Trenaunay-Weber综合征(KTWS)涉及三合会的条件,包括受影响的肢体的皮肤血管瘤,静脉致血清和骨质和软组织肥大。 我们在患有KTWS的患者中描述了中枢神经系统中的多个侧探的罕见情况。 A-64岁的男子患有KTWS和先前的脑出血,突然发作了步态和卵巢紊乱。 磁共振成像扫描显示出与他腰骶部脊髓中出血相关的气孔瘤。 此外,在他的大脑中鉴定了许多潜航。 他保守治疗,没有不良事件。 步态紊乱改善,但植物肠病骚扰没有改善。

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