Seattle Children's Hospital Department of Orthopaedic Surgery, University of Washington Department of Orthopaedics and Sports Medicine, 4800 Sand Point Way NE, Seattle, WA, 98105, USA.
Seattle Children's Hospital Department of Radiology, University of Washington Department of Radiology, Seattle, USA.
Spine Deform. 2021 May;9(3):833-839. doi: 10.1007/s43390-020-00264-5. Epub 2021 Jan 5.
Skeletal dysplasia (SKD) have predictably abnormal occipitocervical skeletal anatomy, but a similar understanding of their vertebral artery anatomy is not known. Knowledge and classification of vertebral artery anatomy in SKD patients is important for safe surgical planning. We aimed to determine if predictably abnormal vertebral artery anatomy exists in pediatric SKD.
We performed a retrospective review of CTAs of the neck for pediatric patients at a single institution from 2006 to 2018. CTAs in SKD and controls were reviewed independently in blinded fashion by two radiologists who classified dominance, vessel curvature at C2, direction at C3, and presence of fenestration and intersegmental artery.
14 skeletal dysplasia patients were compared to 32 controls. The path of the vertebral artery at C2 foramen was no different between the cohorts or by side, right (p = 0.43) or left (p = 0.13), nor for medial or lateral exiting direction from C3 foramen on right (p = 0.82) or left (p = 0.60). Dominance was most commonly neutral in both groups (71% in SKD and 63% in controls). There were no fenestrated nor first intersegmental arteries in our cohort.
No systematic differences were detected between SKD and control patients with respect to vertebral artery anatomy. Nonetheless, surgically relevant variability was observed in both groups. Paying particular attention to the direction of exit at C3 and curvature at C2 with respect to the foramen and vessel dominance are important and easily classifiable abnormalities that both surgeons and radiologists can use to communicate and employ in pre-operative planning.
III.
骨发育不良(SKD)的枕颈骨骼解剖结构通常异常,但对其椎动脉解剖结构的了解并不相同。了解和分类 SKD 患者的椎动脉解剖结构对于安全的手术计划非常重要。我们旨在确定儿科 SKD 患者是否存在可预测的异常椎动脉解剖结构。
我们对单机构 2006 年至 2018 年的颈部 CTA 进行了回顾性研究。两名放射科医生对 SKD 和对照组的 CTA 进行了独立的盲法评估,他们对优势、C2 处血管弯曲度、C3 处方向以及是否存在窗孔和节段间动脉进行了分类。
将 14 名骨骼发育不良患者与 32 名对照组进行比较。椎动脉在 C2 孔处的路径在两组之间或在右侧(p=0.43)或左侧(p=0.13)均无差异,也不存在从 C3 孔向内侧或外侧离开的方向在右侧(p=0.82)或左侧(p=0.60)。优势在两组中最常见的是中立(SKD 组为 71%,对照组为 63%)。在我们的队列中没有发现窗孔或第一节段间动脉。
在椎动脉解剖结构方面,SKD 与对照组患者之间未发现系统性差异。尽管如此,两组都观察到了与手术相关的变异性。特别注意 C3 处的出口方向以及 C2 处的曲率相对于孔和血管优势,这些都是重要的且易于分类的异常情况,外科医生和放射科医生都可以用来进行沟通并在术前计划中使用。
III。