Holmøy Trygve, Skorstad Gjertrud, Røste Line Sveberg, Scheie David, Alvik Kirsti
Department of Neurology, Oslo University Hospital Ullevål, Oslo, Norway.
Clin Neurol Neurosurg. 2009 Oct;111(8):708-12. doi: 10.1016/j.clineuro.2009.06.005. Epub 2009 Jul 17.
We present a 67-year-old non-diabetic male who presented with muscle cramps, paresis, atrophy and fasciculations in the left leg, followed by rapidly progressive muscle stiffness and superimposed spasms which subsequently also affected the right leg and the trunk. GAD65 autoantibodies were elevated in serum and CSF, compatible with systemic and intrathecal synthesis of oligoclonal and high-avidity autoantibodies, and GAD65 specific T cells were clonally expanded in the CSF. The patient did not respond to GABAergic and immunomodulatory treatment or plasma exchange, and died from respiratory failure after 18 months. Autopsy revealed unilateral axonal swelling, chromatolysis and vacuolisation of anterior horn cells of the lower spinal cord, accompanied by microglia proliferation and discrete infiltration of CD8+ cytotoxic T cells. No CD4+ T helper cells, B cells or complement deposition were detected. To our knowledge, this is the first report of stiff person syndrome with lower motor signs restricted to a lower limb, and also the first attempt to characterize the infiltrating T cells. The finding of CD8+ cytotoxic T cells in the absence of B cells in the inflamed area of the spinal cord suggests that the intrathecal synthesis of GAD65 autoantibodies takes place in areas of the CNS not strictly related to the clinically relevant lesions.
我们报告一名67岁非糖尿病男性,其出现左腿肌肉痉挛、轻瘫、萎缩和肌束震颤,随后迅速进展为肌肉僵硬并伴有痉挛,随后右侧腿部和躯干也受影响。血清和脑脊液中GAD65自身抗体升高,符合寡克隆和高亲和力自身抗体的全身及鞘内合成,且脑脊液中GAD65特异性T细胞呈克隆性扩增。该患者对GABA能和免疫调节治疗或血浆置换均无反应,18个月后死于呼吸衰竭。尸检显示脊髓下部前角细胞单侧轴突肿胀、染色质溶解和空泡化,伴有小胶质细胞增殖和CD8 + 细胞毒性T细胞的散在浸润。未检测到CD4 + T辅助细胞、B细胞或补体沉积。据我们所知,这是首例下运动体征局限于下肢的僵人综合征报告,也是首次对浸润性T细胞进行特征描述的尝试。在脊髓炎症区域发现CD8 + 细胞毒性T细胞而无B细胞,提示GAD65自身抗体的鞘内合成发生在中枢神经系统中与临床相关病变无严格关联的区域。