Poh Mervyn Q W, Simon Neil G, Buckland Michael E, Salisbury Elizabeth, Watson Shaun
Department of Neurology, Prince of Wales Hospital, Barker St., Randwick, Australia.
Neuroscience Research Australia, Barker St., Randwick, Australia; Prince of Wales Clinical School, University of New South Wales, Barker St., Randwick, Australia.
J Neurol Sci. 2014 Feb 15;337(1-2):235-7. doi: 10.1016/j.jns.2013.12.015. Epub 2013 Dec 15.
Paraneoplastic stiff-person syndrome (SPS) has been associated with antibodies against amphiphysin. Current evidence supports a pathogenic role for anti-amphiphysin antibodies. A 74-year-old female was diagnosed with amphiphysin-associated paraneoplastic stiff-person syndrome and associated encephalomyelitis. She had initial response to IVIG, however her symptoms worsened after two months and were resistant to further treatment. Subsequently the patient died and a post-mortem was performed. Neuropathology revealed perivascular and parenchymal lymphocytic infiltrates, with neuronophagia mediated by CD8+ T cells and microglia in brainstem, spinal cord, and mesial temporal lobe structures. These findings suggest a pathogenic role of cytotoxic CD8+ T-cells, with potential implication for therapy of future patients.
副肿瘤性僵人综合征(SPS)与抗 amphiphysin 抗体有关。目前的证据支持抗 amphiphysin 抗体的致病作用。一名 74 岁女性被诊断为与 amphiphysin 相关的副肿瘤性僵人综合征及相关脑脊髓炎。她最初对静脉注射免疫球蛋白有反应,然而两个月后症状恶化,对进一步治疗产生耐药。随后患者死亡并进行了尸检。神经病理学显示血管周围和实质淋巴细胞浸润,在脑干、脊髓和颞叶内侧结构中有由 CD8 + T 细胞和小胶质细胞介导的噬神经元现象。这些发现提示细胞毒性 CD8 + T 细胞的致病作用,对未来患者的治疗可能有潜在影响。