自身免疫性脱髓鞘中枢神经系统疾病的年轻男性持续阳性荧光螺旋体抗体吸收试验:1例报告

Mario B Prado , Karen Joy Adiao
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引用次数: 0

摘要

对于NMOSD和MOGAD,发病和复发通常先于非特异性感染,但到目前为止还没有发现与这些疾病密切相关的已知微生物。梅毒作为NMOSD或MOGAD的诱因事件只报道过一次(Wilcox et al., 2008)。本病例报告探讨梅毒是否引发自身免疫性中枢神经系统疾病或自身免疫性中枢神经系统疾病可能导致假阳性确证梅毒螺旋体试验。患者30岁,有8个月的猝发性双下肢痉挛、共济失调及失明病史,影像学证实为横断性脊髓炎,视神经相干断层扫描证实为视神经炎。抗aq4和抗mog均为阴性,但患者反复检测ta - abs呈阳性。我们怀疑,通过分子模仿和旁观者激活,梅毒可能引发了其自身免疫性中枢神经系统脱髓鞘状况的发作和复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoimmune demyelinating central nervous system disease in young male with persistently positive fluorescent treponemal antibody absorption test: A case report
For NMOSD and MOGAD, onset and relapses are often preceded by non-specific infections, but up until now no known microorganism has been identified to be strongly associated with these conditions. Syphilis as inciting event for NMOSD or MOGAD has only been reported once (Wilcox et al., 2008). This case report examines whether syphilis triggers autoimmune CNS condition or autoimmune CNS disease may cause false positive confirmatory treponemal test. The patient is a 30-year-old who came in with 8-month history of sudden onset spasticity and ataxia of bilateral lower extremities and blindness, confirmed to be transverse myelitis via imaging and optic neuritis by optic coherence tomography respectively. Anti-AQ4 and anti-MOG were negative, however, the patient repeatedly tested positive in FTA-ABS. We suspect that through molecular mimicry and bystander activation, there is a possibility that syphilis may have incited the onset and relapse of his autoimmune CNS demyelinating condition.
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