一例与髓样静脉畸形和海绵状畸形相关的患者的致痫性

Q4 Medicine
A. Nishimura, T. Morioka, K. Hashiguchi, M. Mizoguchi, S. Nagata, Satoshi O. Suzuki, Tomio Sasaki
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引用次数: 1

摘要

我们报告一例53岁男性的手术病例,他患有病变性癫痫,并伴有髓样静脉畸形(MVM)和右侧额叶海绵状畸形(CM)。自44岁时右额叶出现mvm相关脑出血以来,他经常发生继发性全身性癫痫发作。术中皮质电图显示CM上方淡黄色皮层有频繁的阵发性活动。前额叶切除术包括刺激皮质、CM、MVM及其分支。手术后病人不再癫痫发作。病理上,CM上方的刺激皮质有含铁血黄素沉积和星形胶质增生。CM周围有不同大小的扩张静脉,表明MVM,这证实了所谓的水母头的放射学表现。CM和MVM患者的致痫性被认为是由于CM反复出血。讨论了手术策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epileptogenicity of a patient with the association of medullary venous malformation and cavernous malformation
We present a surgical case of a 53-year-old man with lesion-related epilepsy associated with medullary venous malformation (MVM) and cavernous malformation (CM) in the right frontal lobe. He had frequent secondary generalized seizures since developing a MVM-related intracerebral hemorrhage in the right frontal lobe at the age of 44. Intraoperative electrocorticography demonstrated frequent paroxysmal activities on the yellowish cortex above the CM. Anterior frontal lobectomy including the irritative cortex, CM, MVM and its tributaries was performed. The patient became seizure free after surgery. Pathologically, the irritative cortex above the CM had hemosiderin deposits and astrogliosis. The CM was surrounded by dilated veins of various sizes, indicating MVM, which confirmed the radiological findings of so-called caput medusae. Epileptogenicity in patients with CM and MVM is thought to be due to repeated hemorrhage from the CM. Surgical strategy is discussed.
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来源期刊
Epilepsy and Seizure
Epilepsy and Seizure Medicine-Neurology (clinical)
CiteScore
1.30
自引率
0.00%
发文量
5
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