首页> 美国卫生研究院文献>Experimental and Therapeutic Medicine >Hybrid surgery for an arteriovenous malformation fed by an accessory middle cerebral artery and drained by a developmental venous anomaly: A case report and literature review
【2h】

Hybrid surgery for an arteriovenous malformation fed by an accessory middle cerebral artery and drained by a developmental venous anomaly: A case report and literature review

机译:混合外科手术治疗脑副动脉供血并发育静脉异常引流的动静脉畸形:病例报告和文献复习

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

An accessory middle cerebral artery (AMCA), which mainly acts in the collateral circulation of the middle cerebral artery (MCA), is a rare anatomic malformation. Similar to other intracranial vessels, cerebrovascular disease can occur in the AMCA. However, the development of an arteriovenous malformation (AVM) in the AMCA is very rare, especially in conjuction with developmental venous anomalies (DVAs). Here, a rare case of an AMCA combined with an AVM and a DVA was reported. The patient was a 47-year-old female with intracranial hemorrhage at symptom onset. CT and MRI showed lesions in the left Sylvian fissure and insula accompanied by hemorrhage. DSA suggested a left AMCA; an AVM of the AMCA was located in the deep Sylvian fissure. The AVM was diffusely developed and drained into the DVA. The operation was performed in a hybrid operating room. The major feeding artery of the AVM, which was derived from the AMCA, was clipped, then the AVM and DVA were subsequently removed. Intraoperative DSA showed that the AVM and DVA were radically removed. A pathological examination confirmed the presence of an AVM. The patient recovered well and was discharged. Therefore, as highlighted in this case report, rare AVMs can be found in AMCAs and can even occur simultaneously with a DVA. Hybrid surgical treatment can be used to remove AVMs and can lead to an improved prognosis.
机译:副大脑中动脉(AMCA)主要在大脑中动脉(MCA)的侧支循环中起作用,是一种罕见的解剖畸形。与其他颅内血管类似,AMCA中可能发生脑血管疾病。但是,AMCA中动静脉畸形(AVM)的发展非常罕见,尤其是与发展性静脉异常(DVA)结合使用时。在此,报告了一种罕见的将AMCA与AVM和DVA相结合的情况。该患者是一名47岁的女性,在症状发作时出现颅内出血。 CT和MRI显示左西尔维亚裂痕和岛状岛皮病灶,并伴有出血。 DSA建议使用左AMCA; AMCA的AVM位于深部的Sylvian裂缝中。 AVM扩散展开并排入DVA。该手术在混合手术室进行。修剪源自AMCA的AVM的主要供血动脉,然后移除AVM和DVA。术中DSA显示AVM和DVA被彻底清除。病理检查证实存在AVM。病人康复好,出院了。因此,如本案例报告所述,在AMCA中可以找到罕见的AVM,甚至可以与DVA同时发生。混合手术治疗可用于去除AVM,并可改善预后。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号