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颅内动脉瘤可能是成骨不全症的一种并发症:病例系列及文献回顾。

Intracranial aneurysm as a possible complication of osteogenesis imperfecta: a case series and literature review.

机构信息

Department of Pediatrics, Osaka Hospital, Japan Community of Healthcare Organization (JCHO), Osaka 553-0003, Japan.

Division of Diabetes, Clinical Nutrition and Endocrinology, Kansai Electric Power Hospital, Osaka 553-0003, Japan.

出版信息

Endocr J. 2023 Jul 28;70(7):697-702. doi: 10.1507/endocrj.EJ22-0620. Epub 2023 May 9.

Abstract

Osteogenesis imperfecta (OI) is an inherited disease characterized by bone fragility due to impaired type I collagen. Although orthopedic management is improving, other complications are poorly understood. We describe three patients with OI with unruptured intracranial aneurysm (IA) detected by magnetic resonance angiography (MRA) screening of 14 patients. Case 1 was a 73-year-old woman with type 1 OI with blue sclera, vertebral compression fractures, and impaired hearing. Lumbar spine bone mineral density (BMD) was preserved (young adult mean (YAM): 86%). MRA revealed an IA in the right internal carotid artery. Case 2 was a 43-year-old man with type 4 OI and leg-length discrepancy due to left femoral neck fracture. Lumbar spine BMD was decreased (YAM: 61%). MRA showed an IA in the left anterior cerebral artery. Case 3 was a 35-year-old woman with type 3 OI with blue sclera, dentinogenesis imperfecta, deformity of the long bones, and severe scoliosis. She had undergone spine surgery and needed wheelchair assistance. The YAM of the femoral neck BMD was 71%. MRA indicated an IA in the right posterior communicating artery. The prevalence of IA in our series of patients with OI was 21%, which is higher than the reported prevalence of unruptured IA in the Japanese general population (2.2%), suggesting that IA may be a complication of OI. Our literature review revealed no cases of OI with unruptured IA, but 11 cases of OI with subarachnoid hemorrhage. IA seems unrelated to OI type, sex, or age. We recommend MRA of adults with OI.

摘要

成骨不全症(OI)是一种遗传性疾病,其特征是由于 I 型胶原受损导致骨骼脆弱。尽管矫形管理正在改善,但其他并发症仍知之甚少。我们描述了 14 例患者中通过磁共振血管造影(MRA)筛查发现的 3 例 OI 伴未破裂颅内动脉瘤(IA)患者。病例 1 为 73 岁女性,患有 1 型 OI,巩膜蓝色,椎体压缩性骨折,听力受损。腰椎骨密度(BMD)正常(青年平均(YAM):86%)。MRA 显示右侧颈内动脉 IA。病例 2 为 43 岁男性,患有 4 型 OI,因左侧股骨颈骨折导致下肢长度差异。腰椎 BMD 降低(YAM:61%)。MRA 显示左侧大脑前动脉 IA。病例 3 为 35 岁女性,患有 3 型 OI,巩膜蓝色,牙本质生成不全,长骨畸形,严重脊柱侧凸。她曾接受过脊柱手术,需要轮椅辅助。股骨颈 BMD 的 YAM 为 71%。MRA 提示右侧后交通动脉 IA。我们 OI 患者系列中的 IA 患病率为 21%,高于日本普通人群未破裂 IA 的报告患病率(2.2%),提示 IA 可能是 OI 的一种并发症。我们的文献复习没有发现 OI 伴未破裂 IA 的病例,但有 11 例 OI 伴蛛网膜下腔出血。IA 似乎与 OI 类型、性别或年龄无关。我们建议对 OI 成人进行 MRA。

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