Goto S, Mochizuki M, Kita T, Murakami M, Nishigaki H, Moriya H
Department of Orthopaedic Surgery, Chiba University School of Medicine, Japan.
Spine (Phila Pa 1976). 1998 Jul 1;23(13):1485-9. doi: 10.1097/00007632-199807010-00010.
A case of a late infantile atlantoaxial rotatory fixation is reported for which transoral anterior release was performed.
To report a patient who underwent transoral anterior release of the dislocated atlantoaxial joint for a case of late infantile atlantoaxial rotatory fixation and quadriparesis.
Infantile atlantoaxial rotatory fixation is diagnosed easily by using recently developed imaging techniques such as computed tomography, magnetic resonance imaging, and three-dimensional computed tomography. Nevertheless, patients in whom the condition has been overlooked still are encountered, and the reduction in these patients becomes impossible by traction or by simple posterior open reduction. Few reports on the management of type II-IV chronic atlantoaxial rotatory fixation in which an anterior surgery was performed exist in the literature, and no report exists in which atlantoaxial joint release on the both sides was attained.
A 9-year-old girl had a type III atlantoaxial rotatory fixation and quadriparesis. She received direct skull traction and repeated manual reduction while she was awake or under general anesthesia. Neither reduction nor movement was obtained, according to the radiographs. Therefore, it was necessary to perform open reduction posteriorly and transorally to release the fixed and contracted joints between C1 and C2.
After the anterior release of the joints, there was an inherent force preventing a complete rotational reduction. However, after a successful posterior reduction and fusion, and for more than 4 years after surgery, neither rotatory displacement nor neurologic deterioration was noted.
The authors suggest that careful transoral anterior release of the atlantoaxial joint permits successful reduction in a case of chronic fixed atlantoaxial rotatory fixation combined with cord compression.
报告一例晚期婴儿型寰枢椎旋转固定病例,该病例接受了经口前路松解术。
报告一例因晚期婴儿型寰枢椎旋转固定和四肢瘫而接受经口前路松解脱位的寰枢关节的患者。
利用计算机断层扫描、磁共振成像和三维计算机断层扫描等最新开发的成像技术,婴儿型寰枢椎旋转固定很容易诊断。然而,仍有一些患者的病情被忽视,这些患者无法通过牵引或简单的后路切开复位来实现复位。文献中很少有关于II-IV型慢性寰枢椎旋转固定行前路手术治疗的报道,也没有关于双侧寰枢关节松解的报道。
一名9岁女孩患有III型寰枢椎旋转固定和四肢瘫。她在清醒或全身麻醉下接受了直接颅骨牵引和反复手法复位。根据X线片,复位和活动均未成功。因此,有必要进行后路切开复位和经口松解C1和C2之间固定和挛缩的关节。
关节前路松解后,存在一种内在力量阻止完全旋转复位。然而,在成功进行后路复位和融合后,以及术后4年多,均未发现旋转移位或神经功能恶化。
作者认为,对于慢性固定性寰枢椎旋转固定合并脊髓压迫的病例,仔细的经口前路松解寰枢关节可实现成功复位。