Department of Neurosurgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, 226014, Uttar Pradesh, India.
Acta Neurochir (Wien). 2013 Jul;155(7):1157-67. doi: 10.1007/s00701-013-1717-x. Epub 2013 May 5.
This prospective study attempts to study the clinico-radiological differences between patients with syndromic AAD (SAAD), non-syndromic AAD (NSAAD), and AAD with Klippel-Feil anomaly (AADKFA) that may impact management.
In 46 patients with AAD [SAAD (including Morquio, Down, Larson and Marshall syndrome and achondroplasia; n = 6); NSAAD(n = 20); and, AADKFS (n = 20)], myelopathy was graded as mild (n = 17, 37 %), moderate (15, 32.5 %) or severe (14, 30.5 %) based on Japanese Orthopaedic Association Score modified for Indian patients (mJOAS). Basilar invagination (BI), basal angle, odontoid hypoplasia, facet-joint angle, effective canal diameter, Ishihara curvature index, and angle of retroversion of odontoid and vertebral artery (VA) variations were also studied.
Clinico-radiological differences were assessed by Fisher's exact test, and mean craniometric values by Kruskal-Wallis test (p value ≤ 0.05 significant)
Incidence of irreducible AAD in SAAD (n = 0), NSA AD (11.55 %) and AADKFS (n = 18.90 %) showed significant difference (p = 0.01). High incidence of kyphoscoliosis (83 %) and odontoid hypoplasia (83 %) in SAAD, and assimilated atlas and BI in NSAAD and AADKFA groups were found. In AADKFA, effective canal diameter was significantly reduced(p = 0.017) with increased Ishihara index and increased angle of odontoid retroversion; 61 % patients had VA variations. Thirty-five patients underwent single-stage transoral decompression with posterior fusion (for irreducible AAD) or direct posterior stabilization (for reducible AAD). Postoperative mJOAS evaluation often revealed persistent residual myelopathy despite clinical improvement.
Myelopathy is induced by recurrent cord trauma due to reducible AAD in SAAD, and compromised cervicomedullary canal diameter in NSAAD and AADKFA. SAAD in children may be missed due to incomplete odontoid ossification or coexisting angular deformities. In AADKFA, decisions regarding vertebral levels to be included in posterior stabilization should take into consideration intact intervening motion segments and compensatory cervical hyperlordosis. Following VA injury, endovascular primary vessel occlusion/stenting across pseudoaneurysm preempts delayed rehemorrhage.
本前瞻性研究旨在探讨综合征型 Arnold-Chiari 畸形(SAAD)、非综合征型 Arnold-Chiari 畸形(NSAAD)和伴有 Klippel-Feil 异常的 Arnold-Chiari 畸形(AADKFA)患者之间可能影响治疗的临床-影像学差异。
在 46 例 Arnold-Chiari 畸形患者中(SAAD[包括 Morquio、Down、Larson 和 Marshall 综合征和软骨发育不全;n=6];NSAAD[n=20];AADKFS[n=20]),根据改良的印度患者日本矫形协会评分(mJOAS)将脊髓病分为轻度(n=17,37%)、中度(15,32.5%)或重度(14,30.5%)。还研究了基底凹陷(BI)、基底角、齿状突发育不全、关节突关节角、有效椎管直径、Ishihara 曲率指数和齿状突与椎动脉(VA)变异的后旋角度。
Fisher 确切检验评估临床-影像学差异,Kruskal-Wallis 检验评估颅测量值(p 值≤0.05 为有统计学意义)。
SAAD(n=0)、NSAAD(11.55%)和 AADKFS(n=18.90%)患者中不可复位 Arnold-Chiari 畸形的发生率存在显著差异(p=0.01)。SAAD 患者高发生率的脊柱侧凸(83%)和齿状突发育不全(83%),以及 NSAAD 和 AADKFA 组中融合的寰椎和 BI。在 AADKFA 中,有效椎管直径明显减小(p=0.017),Ishihara 指数增加,齿状突后旋角度增加;61%的患者存在 VA 变异。35 例患者接受了一期经口减压联合后路融合(用于不可复位 Arnold-Chiari 畸形)或直接后路稳定(用于可复位 Arnold-Chiari 畸形)。尽管临床症状改善,但术后 mJOAS 评估常显示持续存在残留的脊髓病。
SAAD 中的可复位 Arnold-Chiari 畸形导致反复脊髓损伤,而 NSAAD 和 AADKFA 中的颈髓管直径减小导致脊髓病。由于齿状突未完全骨化或并存的角度畸形,儿童期的 SAAD 可能会被漏诊。在 AADKFA 中,决定后路稳定时要包括哪些椎体,应考虑到完整的节段间运动和代偿性颈椎过度前凸。VA 损伤后,血管内原发性血管闭塞/支架置入穿过假性动脉瘤可预防延迟性再出血。