血管造影证实全切除后脑动静脉畸形会复发吗?

Hashimoto, Nozaki
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引用次数: 62

摘要

脑动静脉畸形(AVMs)被认为是由于胚胎发育失败导致原始血管通道向成熟动脉、毛细血管和静脉的正常分化。虽然这些本质上是先天性血管畸形,但在最近的文献中也报道了明显的脑动静脉畸形扩大和/或复发。我们使用MEDLINE(1966- 1998)检索脑动静脉畸形的复发情况,分析所有手术切除和术后血管造影阴性后的复发病例,并讨论脑动静脉畸形复发的机制。一项全面的文献调查显示,只有12例复发病例(9例用英文记录,3例用日文记录),这表明脑动静脉畸形的复发率很罕见,尽管由于缺乏常规的长期随访,实际复发率尚不清楚。复发性脑动静脉畸形的部位均为大脑半球,首发表现均为出血。11例患者中有9例在20岁以下复发,提示脑动静脉畸形在未成熟的脑血管中有复发的倾向。目前还没有明确的机制来解释为什么先天性异常,如脑动静脉畸形在完全切除后复发,但最近提出了两个似是而非的机制。一种是血管内皮生长因子(VEGF)对血管生成的失调,另一种是一种新的解剖实体,“隐藏腔室”。虽然VEGF是主要的血管生成因子之一,在胎儿脑和病理性新生血管中发挥着重要作用,但VEGF的合成可能不足以解释脑avm的复发,因为在非复发患者中也发现了VEGF阳性染色。隐藏腔室是血管造影未填充的腔室,尽管进行了充分的检查,但可能位于血管造影显示的AVM内部、邻近或相对较远。虽然它可以解释未解决的临床现象,如再生、复发、术前或术后意外出血和脑肿胀,但隐藏腔室的存在应通过高分辨率放射检查或手术中证实。现代显微外科技术完全切除脑动静脉后出现复发,提示术后早期脑血管造影作为评估脑动静脉消失的金标准,不足以消除出血的风险,应计划仔细的长期随访研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do cerebral arteriovenous malformations recur after angiographically confirmed total extirpation?

Cerebral arteriovenous malformations (AVMs) are thought to result from a failure of embryogenesis in the otherwise normal differentiation of primordial vascular channels into mature arteries, capillaries, and veins. Although these are essentially congenital vascular malformations, marked enlargement and/or recurrence of cerebral AVMs has been reported in the recent literature. Using MEDLINE (1966- 1998), we searched the recurrence of cerebral AVMs and analyzed all reported recurrent cases after total surgical extirpation and negative postoperative angiogram, and discussed the proposed mechanisms of the recurrence of cerebral AVMs. A thorough literature survey disclosed only 12 documented recurrent cases (9 were documented in English and 3 in Japanese), which shows the rarity of the recurrence of cerebral AVMs, although the actual rate of recurrence is not known because of the lack of routine long-term follow-up. The location of recurrent cerebral AVMs was the cerebral hemisphere, and initial presentation was hemorrhage in all cases. Recurrence occurred in patients under 20 years of age in 9 of 11 cases, which implies the propensity of recurrence of cerebral AVMs in immature brain vasculature. There are no definite proven mechanisms to explain why congenital anomalies such as cerebral AVMs recur after total extirpation, but recently two plausible mechanisms have been proposed. One is angiogenesis disregulated by vas-cular endothelial growth factor (VEGF) and the other is a new anatomical entity, 'hidden compart-ments'. Although VEGF is one of the main angiogenetic factors and its important role in fetal brain and pathological neovascularization has been reported, the synthesis of VEGF might be insufficient to explain the recurrence of cerebral AVMs because VEGF-positive staining is also found in nonrecurrent patients. Hidden compartments are angiographically unfilled compartments, in spite of an adequate examination, which may be located within, contiguous with, or relatively far from the angiographically demonstrated AVM. Although it might explain unsolved clinical phenomena such as regrowth, recurrence, and per- or postoperative unanticipated bleeding and brain swelling, the existence of hidden compartments should be proved by high-resolution radiological examinations or during operations. The presence of recurrent cerebral AVMs after complete extirpation by modern microsurgical techniques indicates that cerebral angiography in the early postoperative stage, the golden standard to assess the disappearance of cerebral AVMs, is not sufficient to eliminate the risk of hemorrhage, and careful long-term follow-up studies should be planned.

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