RT期刊文章SR电子T1 Amphiphysin-IgG自身免疫性神经病变摩根富林明神经学神经学乔FD Lippincott Williams &威尔金斯首页SP e1873 OP e1880 10.1212 / WNL。93签证官0000000000008472是20 A1 Divyanshu Dubey A1 Jiraporn Jitprapaikulsan A1支Bi A1 Rocio巴斯克斯做Campo A1安德鲁·麦肯A1肖恩·j·Pittock A1 Janean k Engelstad A1约翰·r·米尔斯A1克里斯托弗·j·克莱因年2019 UL //www.ez-admanager.com/content/93/20/e1873.abstract AB目标定义的临床病首页理的特点amphiphysin-immunoglobulin G(免疫球蛋白)介导的神经病变。方法患者检查在我们的机构从1月1日,1995年9月30日,2018年,与amphiphysin-IgG通过间接免疫荧光和免疫印迹,综述。相比他们的表型的共存collapsin response-mediator protein-5 (CRMP5)免疫球蛋白或anti-neuronal核1型(ANNA1-IgG)和CRMP5-IgG自身免疫抗体。改善改良Rankin规模(夫人)(≥1)后续被认为是一个有利的结果。Amphiphysin RNA表达在健康评估神经。结果53 amphiphysin-IgG-positive病例。神经病变患者33例(60%),21个amphiphysin-IgG孤独,和12个共存自身抗体(ANNA1-IgG n = 8;CRMP5-IgG, n = 2;ANNA1-IgG CRMP5-IgG, n = 2)。在孤立amphiphysin-IgG自身免疫系统疾病包括多神经根神经病(62%)、弥漫性感官neuronopathy(35%),与胃轻瘫和面部神经病变(3%)。其中,疼痛(80%)、乳腺癌(63%),对中枢神经系统(57%)责任人通常共存,和神经病变常常引起乳腺癌的诊断(76%)。 Stiff-person spectrum disorder was the most common CNS accompaniment (45%). Nerve biopsies showed axonal loss (n = 6/6), subperineurial edema (n = 4/6), and CD4 predominant inflammation (n = 2/6). Median mRS score at last follow-up was 3.5; 58% of patients were immunotherapy-responsive. Patients with amphiphysin-IgG alone had more favorable immunotherapy response than patients with CRMP5-IgG polyneuropathy (n = 45) (44% vs 16%, p = 0.028, odds ratio 4.2, 95% confidence interval 1.1 to 15.5). Only 1/9 (11%) patients with amphiphysin-IgG with coexisting CRMP5-IgG or ANNA1-IgG had immunotherapy response. RNA amphiphysin expression occurred at low levels in nerve.Conclusion Amphiphysin-IgG autoimmune neuropathy has a recognizable phenotype, is frequently immune responsive, and can prompt early diagnosis of breast cancer.ANNA1=antineuronal nuclear antibody type 1; CRMP5=collapsin response-mediator protein-5; IgG=immunoglobulin G; IIF=indirect immunofluorescence; mRS=modified Rankin Scale; PBS=phosphate-buffered saline; RT=room temperature

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