Subarachnoid hemorrhage secondary to ruptured posterior inferior cerebellar artery aneurysm in a patient with type 3 osteogenesis imperfecta: A case report and topic review.

Surgical neurology international Pub Date : 2025-08-15 eCollection Date: 2025-01-01 DOI:10.25259/SNI_611_2025

Segev Gabay, Ariel Agur, Oz Haim

{"title":"Subarachnoid hemorrhage secondary to ruptured posterior inferior cerebellar artery aneurysm in a patient with type 3 osteogenesis imperfecta: A case report and topic review.","authors":"Segev Gabay, Ariel Agur, Oz Haim","doi":"10.25259/SNI_611_2025","DOIUrl":null,"url":null,"abstract":"Background: Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by collagen Type I deficiency, leading to bone fragility, skeletal deformities, and, less commonly, vascular abnormalities. Cerebrovascular complications in OI are rare. There are few reports of subarachnoid hemorrhage (SAH) secondary to ruptured aneurysms in OI patients, particularly involving the posterior circulation.Case description: We present a unique scenario of a long-term survivor, a female patient, with Type III OI who experienced a spontaneous SAH due to a ruptured posterior inferior cerebellar artery aneurysm.Conclusion: Given the patient's underlying OI, special neurosurgical and endovascular techniques were employed to ensure safe aneurysm coiling and cerebrospinal fluid diversion. We outline these challenges faced in the management of such a patient and provide a literature review to contextualize our findings.","PeriodicalId":94217,"journal":{"name":"Surgical neurology international","volume":"16 ","pages":"342"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12482725/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surgical neurology international","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/SNI_611_2025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

Abstract

Background: Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by collagen Type I deficiency, leading to bone fragility, skeletal deformities, and, less commonly, vascular abnormalities. Cerebrovascular complications in OI are rare. There are few reports of subarachnoid hemorrhage (SAH) secondary to ruptured aneurysms in OI patients, particularly involving the posterior circulation.

Case description: We present a unique scenario of a long-term survivor, a female patient, with Type III OI who experienced a spontaneous SAH due to a ruptured posterior inferior cerebellar artery aneurysm.

Conclusion: Given the patient's underlying OI, special neurosurgical and endovascular techniques were employed to ensure safe aneurysm coiling and cerebrospinal fluid diversion. We outline these challenges faced in the management of such a patient and provide a literature review to contextualize our findings.

查看原文本刊更多论文

3型成骨不全患者后下小脑动脉瘤破裂继发蛛网膜下腔出血1例报告及主题回顾。

背景：成骨不全症（Osteogenesis imperfecta， OI）是一种罕见的遗传性疾病，以I型胶原缺乏为特征，导致骨骼脆弱、骨骼畸形，以及少见的血管异常。成骨不全的脑血管并发症是罕见的。在成骨不全患者中，继发于动脉瘤破裂的蛛网膜下腔出血（SAH）的报道很少，特别是累及后循环。病例描述：我们报告了一个长期幸存者的独特情况，一名女性III型成骨不全症患者，由于小脑后下动脉瘤破裂而发生自发性SAH。结论：考虑到患者潜在的成骨不全，采用特殊的神经外科和血管内技术来确保动脉瘤卷取和脑脊液转移的安全。我们概述了在管理这类患者时所面临的挑战，并提供了一份文献综述来说明我们的发现。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Surgical neurology international

自引率

0.00%

发文量