Birnbaum Julius, Lalji Aliya, Piccione Ezequiel A, Izbudak Izlem
Division of Rheumatology and Department of Neurology, The Johns Hopkins University School of Medicine The Johns Hopkins University School of Medicine, Baltimore, MD Department of Neurological Sciences, University of Nebraska Medical Center, Omaha, NE Division of Neuroradiology, Department of Radiology and Radiological Sciences, The Johns Hopkins University School of Medicine, Baltimore, MD.
Medicine (Baltimore). 2017 Dec;96(49):e8483. doi: 10.1097/MD.0000000000008483.
Sensory neuronopathy can be a devastating peripheral nervous system disorder. Profound loss in joint position is associated with sensory ataxia, and reflects degeneration of large-sized dorsal root ganglia. Prompt recognition of sensory neuronopathies may constitute a therapeutic window to intervene before there are irreversible deficits. However, nerve-conduction studies may be unrevealing early in the disease course. In such cases, the appearance of dorsal column lesions on spinal-cord MRI can help in the diagnosis. However, most studies have not defined whether such dorsal column lesions may occur within earlier as well as chronic stages of sensory neuronopathies, and whether serial MRI studies can be used to help assess treatment efficacy. In this case-series of three sensory neuronopathy patients, we report clinical characteristics, immunological markers, nerve-conduction and skin-biopsy studies, and neuroimaging features.
All three patients presented with characteristic features of sensory neuronopathy with abnormal spinal-cord MRI studies. Radiographic findings included non-enhancing lesions in the dorsal columns that were longitudinally extensive (spanning ≥ 3 vertebral segments).
All patients had anti-Ro/SS-A and/or anti-La/SS-B antibodies, with patients one and two having Sjögren's syndrome. MRI findings were similar when performed in the earlier stages of a sensory neuronopathy (patient one, after four months) and chronic stages (patients two and three, after five and three years, respectively).
Patient one was treated with rituximab combined with intravenous immunoglobulin therapy.
Patient one was initially wheelchair-bound and had improved ambulation after treatment. In this patient, serial MRI studies revealed partial resolution of dorsal column lesions, associated with decreased sensory ataxia and improved nerve-conduction studies.
In addition to vitamin B12 and copper deficiency, it is important to include sensory neuronopathies in the differential diagnosis of dorsal column lesions. MRI spinal-cord lesions have similar appearances in the earlier as well as chronic phases of a sensory neuronopathy, and therefore suggest that such dorsal column lesions may reflect inflammatory as well as a gliotic burden of injury. MRI may also be a useful longitudinal indicator of treatment response.
感觉神经元病可能是一种严重的周围神经系统疾病。关节位置觉的严重丧失与感觉性共济失调相关,反映了大型背根神经节的退变。及时识别感觉神经元病可能为在出现不可逆缺陷之前进行干预提供一个治疗窗口。然而,在疾病早期神经传导研究可能无异常发现。在这种情况下,脊髓MRI上背柱病变的出现有助于诊断。然而,大多数研究尚未明确这种背柱病变是否可能出现在感觉神经元病的早期以及慢性阶段,以及连续的MRI研究是否可用于帮助评估治疗效果。在这个包含三名感觉神经元病患者的病例系列中,我们报告了临床特征、免疫标志物、神经传导和皮肤活检研究以及神经影像学特征。
所有三名患者均表现出感觉神经元病的特征性表现,脊髓MRI检查异常。影像学表现包括背柱内无强化病变,病变纵向广泛(跨越≥3个椎体节段)。
所有患者均有抗Ro/SS - A和/或抗La/SS - B抗体,患者1和患者2患有干燥综合征。在感觉神经元病的早期阶段(患者1,4个月后)和慢性阶段(患者2和患者3,分别在5年和3年后)进行MRI检查时,结果相似。
患者1接受了利妥昔单抗联合静脉注射免疫球蛋白治疗。
患者1最初需依赖轮椅,治疗后步行能力有所改善。在该患者中,连续的MRI研究显示背柱病变部分消退,同时感觉性共济失调减轻,神经传导研究结果改善。
除了维生素B12和铜缺乏外,在背柱病变的鉴别诊断中纳入感觉神经元病很重要。脊髓MRI病变在感觉神经元病的早期和慢性阶段表现相似,因此提示这种背柱病变可能反映了炎症以及胶质增生性损伤负担。MRI也可能是治疗反应的有用纵向指标。