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症状性非压迫性运动神经元病是强直性脊柱炎的早期表现。

Symptomatic noncompressive motoromyelopathy presents as early manifestation in ankylosing spondylitis.

机构信息

Department of Neurology, Chang Gung Memorial Hospital-Kaohsiung Medical Center and College of Medicine, Chang Gung University, 123 Tai Pei Road, Niao Sung Hsiang, Kaohsiung, 833, Taiwan.

出版信息

Rheumatol Int. 2011 Jul;31(7):945-50. doi: 10.1007/s00296-010-1614-z. Epub 2010 Nov 2.

Abstract

Ankylosing spondylitis (AS) is an autoimmune spondyloarthropathy involving principally the sacroiliac joint and axial skeleton. Spinal cord involvement is an infrequent and late complication. It mostly results from compressive myelopathy due to skeletal osteopathy and usually presents with radiculomyelopathic sensory and motor deficits. To report three patients who suffered a progressive paraparesis/tetraparesis compatible with motor myelopathy without typical skeletal symptom. Myelopathy of unknown origin was initially interpreted in these patients. Radiography did not show typical change at sacroiliac joint or vertebrate. Spinal magnetic resonance image revealed cord atrophy at cervical and thoracic segment. A positivity of B27 antigen was found afterward. Their spondyloarthropathic symptoms developed within six months later with radiographic sacroiliitis. Seropositive AS with noncompressive myelopathy was finally established. Patients showed a reverse of motor impairment when their pain was well undercontrolled. Motor myelopathy may be neglected or underestimated in AS, in especially when typical skeletal symptom is absent or minimal. It may progress surreptitiously to harm spinal function or superimpose to crippling disability in compressive spinal cord injury. Therefore, a careful evaluation and monitor of spinal cord function is important for AS patient despite spinal deformity is not observed.

摘要

强直性脊柱炎(AS)是一种主要累及骶髂关节和中轴骨骼的自身免疫性脊柱关节病。脊髓受累是一种罕见且较晚的并发症。它主要由骨骼病变引起的压迫性脊髓病引起,通常表现为神经根性脊髓病的感觉和运动功能障碍。报告 3 例患者,他们出现进行性截瘫/四肢瘫痪,与运动性脊髓病一致,但无典型骨骼症状。这些患者最初被诊断为原因不明的脊髓病。影像学检查未显示骶髂关节或脊椎有典型变化。脊髓磁共振成像显示颈段和胸段脊髓萎缩。随后发现 B27 抗原阳性。他们的脊柱关节病症状在 6 个月后出现,影像学检查显示骶髂关节炎。最终诊断为血清阳性的非压迫性脊髓病的强直性脊柱炎。当患者的疼痛得到很好控制时,运动功能障碍得到逆转。在没有典型骨骼症状或骨骼症状轻微的情况下,运动性脊髓病可能会被忽视或低估。它可能会偷偷地进展,损害脊髓功能,或在压迫性脊髓损伤导致残疾的基础上进一步加重残疾。因此,即使没有观察到脊柱畸形,对脊柱关节病患者的脊髓功能进行仔细评估和监测也很重要。

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