Morio Yasuo, Yoshioka Takeshi, Nagashima Hideki, Hagino Hiroshi, Teshima Ryota
Department of Orthopaedic Surgery, Tottori University, Faculty of Medicine, Yonago, Japan.
Spine (Phila Pa 1976). 2003 Dec 1;28(23):E492-5. doi: 10.1097/01.BRS.0000099095.21233.5C.
The first case of intraspinal synovial cyst communicating with the C1-C2 facet joints and subarachnoid space associated with rheumatoid atlantoaxial instability is presented.
To describe the diagnosis and successful treatment of a synovial cyst of the C1-C2 junction in a patient with rheumatoid arthritis and atlantoaxial instability.
Intraspinal synovial cysts of the C1-C2 junction are extremely rare. Neither association with rheumatoid atlantoaxial instability nor communication with the C1-C2 facet joints and the subarachnoid space has been previously reported in a synovial cyst of the C1-C2 junction.
The clinical and radiologic features of a 71-year-old woman with a symptomatic synovial cyst of the C1-C2 junction with rheumatoid atlantoaxial instability are detailed. Posterior atlantoaxial fusion alone was performed.
Preoperative magnetic resonance images demonstrated a large cystic mass around the dens, compressing the spinal cord. The mass was of low signal intensity on T1-weighted images, was of high signal intensity on T2-weighted images, and was enhanced marginally with gadolinium-DTPA on T1-weighted images. Computed tomograms performed after myelography disclosed the cyst around the dens communicating with the subarachnoid space and the C1-C2 facet joints. Spontaneous regression of the cyst was identified on the magnetic resonance images 3 months after surgery. One year after surgery, myelopathic symptoms were improved.
An intraspinal cyst communicating with the C1-C2 facet joints and subarachnoid space associated with rheumatoid atlantoaxial instability was reported. Computed tomograms after myelography were useful in delineating the relationships among the synovial cyst, facet joints, and the subarachnoid space. Spontaneous regression of the cyst and clinical improvement were achieved by C1-C2 posterior fusion alone.
报告了首例与类风湿性寰枢椎不稳相关的、与C1-C2关节突关节及蛛网膜下腔相通的脊髓内滑膜囊肿。
描述一名患有类风湿性关节炎和寰枢椎不稳患者C1-C2交界处滑膜囊肿的诊断及成功治疗。
C1-C2交界处的脊髓内滑膜囊肿极为罕见。此前未见有C1-C2交界处滑膜囊肿与类风湿性寰枢椎不稳相关,或与C1-C2关节突关节及蛛网膜下腔相通的报道。
详细介绍了一名71岁有症状的C1-C2交界处滑膜囊肿合并类风湿性寰枢椎不稳女性患者的临床及影像学特征。仅行后路寰枢椎融合术。
术前磁共振成像显示齿状突周围有一巨大囊性肿物,压迫脊髓。该肿物在T1加权像上呈低信号强度,在T2加权像上呈高信号强度,在T1加权像上经钆喷酸葡胺增强后边缘强化。脊髓造影后行计算机断层扫描显示齿状突周围囊肿与蛛网膜下腔及C1-C2关节突关节相通。术后3个月磁共振成像显示囊肿自发消退。术后1年,脊髓病症状改善。
报告了一例与类风湿性寰枢椎不稳相关、与C1-C2关节突关节及蛛网膜下腔相通的脊髓内囊肿。脊髓造影后的计算机断层扫描有助于明确滑膜囊肿、关节突关节及蛛网膜下腔之间的关系。仅通过C1-C2后路融合术实现了囊肿的自发消退及临床改善。