Coexistence of intracranial dysraphic cyst and aneurysm: A qualitative systematic review and multiple management portraits

IF 0.4 Q4 CLINICAL NEUROLOGY
Francesco Calvanese , Anna Maria Auricchio , Anni Pohjola , Rahul Raj , Mika Niemelä
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引用次数: 0

Abstract

Background

The coexistence of intracranial aneurysms and dysraphic cysts is a rare manifestation. The response triggered by the cyst and its proinflammatory content could play a role in the rupture or growth of a neighboring aneurysm.

Methods

We performed a systematic review according to the PRISMA guidelines searching PubMed, Medline, Google Scholar and Embase. Additionally, we report a case of one patient with both a dermoid cyst and an ipsilateral anterior cerebral artery aneurysm, illustrating a progressive formation of the vascular lesion during the follow-up of the cyst.

Results

Out of 103 papers fulfilling the inclusion criteria for the systematic review, 79 articles were selected for eligibility. Finally, a total of 9 cases, including our own case, were considered for the review. We found that all aneurysms were in the anterior circulation and all cysts were supratentorial. The aneurysms or parent vessels were in proximity or in contact with the dysraphic lesion, presenting a strong adherence to its capsule. The 3 dermoids presented with cysts rupture and showed simultaneous or delayed subarachnoid aneurysmal hemorrhage. Two epidermoid cysts were diagnosed after aneurysm rupture, while the others due to focal mass effect, as in the case of the neurenteric cyst.

Conclusions

Coexistence of intracranial aneurysm and disraphic cyst is a rare finding with multiple possible presentations. In managing patients harboring disraphic cyst, the presence of the aneurysm should be ruled out during the standard workup. A coexistence of these pathologies could affect their natural histories, and this could justify a more active management protocol.

颅内发育不良囊肿与动脉瘤并存:定性系统回顾和多种管理画像
背景颅内动脉瘤和畸形囊肿同时存在是一种罕见的表现。方法我们按照 PRISMA 指南检索了 PubMed、Medline、Google Scholar 和 Embase,进行了系统性综述。此外,我们还报告了一例同时患有蝶窦囊肿和同侧大脑前动脉动脉瘤的患者,说明在囊肿的随访过程中,血管病变逐渐形成。结果在103篇符合系统综述纳入标准的论文中,有79篇被选中。最后,包括我们自己的病例在内,共有 9 个病例被纳入审查范围。我们发现,所有动脉瘤均位于前循环,所有囊肿均位于幕上。动脉瘤或母体血管靠近或接触硬膜病变,与其囊肿有很强的粘连性。3 个表皮样囊肿伴有囊肿破裂,并同时或延迟出现蛛网膜下腔动脉瘤出血。有两个表皮样囊肿是在动脉瘤破裂后被诊断出来的,而其他囊肿则是由于局灶性肿块效应引起的,如神经根囊肿的病例。在处理患有椎管内囊肿的患者时,应在标准检查中排除动脉瘤的存在。这些病变同时存在可能会影响其自然病史,因此有理由采取更积极的治疗方案。
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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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