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结缔组织遗传性疾病患者的枕寰枢椎活动过度、颅骨沉降和Ⅰ型Chiari畸形综合征

Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue.

作者信息

Milhorat Thomas H, Bolognese Paolo A, Nishikawa Misao, McDonnell Nazli B, Francomano Clair A

机构信息

Department of Neurosurgery, The Chiari Institute, Harvey Cushing Institute of Neuroscience, North Shore-Long Island Jewish Health System, Manhasset, New York 11030, USA.

出版信息

J Neurosurg Spine. 2007 Dec;7(6):601-9. doi: 10.3171/SPI-07/12/601.

Abstract

OBJECT

Chiari malformation Type I (CM-I) is generally regarded as a disorder of the paraxial mesoderm. The authors report an association between CM-I and hereditary disorders of connective tissue (HDCT) that can present with lower brainstem symptoms attributable to occipitoatlantoaxial hypermobility and cranial settling.

METHODS

The prevalence of HDCT was determined in a prospectively accrued cohort of 2813 patients with CM-I. All patients underwent a detailed medical and neuroradiological workup that included an assessment of articular mobility. Osseous structures composing the craniocervical junction were investigated morphometrically using reconstructed 3D computed tomography and plain x-ray images in 114 patients with HDCT/CM-I, and the results were compared with those obtained in patients with CM-I (55 cases) and healthy control individuals (55 cases).

RESULTS

The diagnostic criteria for Ehlers-Danlos syndrome and related HDCT were met in 357 (12.7%) of the 2813 cases. Hereditability was generally compatible with a pattern of autosomal dominant transmission with variable expressivity. The diagnostic features of HDCT/CM-I were distinguished from those of CM-I by clinical stigmata of connective tissue disease, a greater female preponderance (8:1 compared with 3:1, p < 0.001), and a greater incidence of lower brainstem symptoms (0.41 compared with 0.11, p < 0.001), retroodontoid pannus formation (0.71 compared with 0.11, p < 0.001), and hypoplasia of the oropharynx (0.44 compared with 0.02, p < 0.001). Measurements of the basion-dens interval, basion-atlas interval, atlas-dens interval, dens-atlas interval, clivus-atlas angle, clivus-axis angle, and atlas-axis angle were the same in the supine and upright positions in healthy control individuals and patients with CM-I. In patients with HDCT/CM-I, there was a reduction of the basion-dens interval (3.6 mm, p < 0.001), an enlargement of the basion-atlas interval (3.0 mm, p < 0.001), and a reduction of the clivus-axis angle (10.8 degrees, p < 0.001), clivus-atlas angle (5.8 degrees, p < 0.001), and atlas-axis angle (5.3 degrees, p < 0.001) on assumption of the upright position. These changes were reducible by cervical traction or returning to the supine position.

CONCLUSIONS

The identification of HDCT in 357 patients with CM-I establishes an association between two presumably unrelated mesodermal disorders. Morphometric evidence in this cohort-cranial settling, posterior gliding of the occipital condyles, and reduction of the clivus-axis angle, clivus-atlas angle, and atlas-axis angle in the upright position-suggests that hypermobility of the occipitoatlantal and atlantoaxial joints contributes to retroodontoid pannus formation and symptoms referable to basilar impression.

摘要

目的

I型Chiari畸形(CM-I)通常被认为是一种轴旁中胚层疾病。作者报告了CM-I与结缔组织遗传性疾病(HDCT)之间的关联,后者可表现出因枕寰枢椎活动过度和颅骨沉降导致的下脑干症状。

方法

在一个前瞻性纳入的2813例CM-I患者队列中确定HDCT的患病率。所有患者均接受了详细的医学和神经放射学检查,包括关节活动度评估。使用重建的三维计算机断层扫描和平片x线图像对114例HDCT/CM-I患者构成颅颈交界区的骨性结构进行形态测量,并将结果与CM-I患者(55例)和健康对照者(55例)的结果进行比较。

结果

2813例病例中有357例(12.7%)符合埃勒斯-当洛综合征及相关HDCT的诊断标准。遗传模式通常符合具有可变表达性的常染色体显性遗传模式。HDCT/CM-I的诊断特征与CM-I的诊断特征的区别在于结缔组织病的临床体征、女性占比更高(8:1对比3:1,p<0.001)、下脑干症状发生率更高(0.41对比0.11,p<0.001)、齿突后血管翳形成(0.71对比0.11,p<0.001)以及口咽发育不全(0.44对比0.02,p<0.001)。健康对照者和CM-I患者仰卧位和直立位时的颅底-齿突间距、颅底-寰椎间距、寰椎-齿突间距、齿突-寰椎间距、斜坡-寰椎角、斜坡-枢椎角和寰椎-枢椎角测量值相同。在HDCT/CM-I患者中,直立位时颅底-齿突间距减小(3.6mm,p<0.001),颅底-寰椎间距增大(3.0mm,p<0.001),斜坡-枢椎角(10.8度,p<0.001)、斜坡-寰椎角(5.8度,p<0.001)和寰椎-枢椎角(5.3度,p<0.001)减小。这些变化可通过颈部牵引或恢复仰卧位而减轻。

结论

在357例CM-I患者中发现HDCT,确立了两种可能不相关的中胚层疾病之间的关联。该队列中的形态测量证据——颅骨沉降、枕髁后移以及直立位时斜坡-枢椎角、斜坡-寰椎角和寰椎-枢椎角减小——表明枕寰和寰枢关节活动过度导致齿突后血管翳形成和基底压迹相关症状。

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