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ACUTE-ONSET CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY: AN ELECTRODIAGNOSTIC STUDY

机译:急性发作性慢性炎症性脱发性多发性神经病:电诊断研究

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摘要

Acute-onset chronic inflammatory demyelinating polyneuropathy (A-CIDP) is an increasingly recognized CIDP subtype. Differentiating A-CIDP from Guillain-Barre syndrome (GBS) is challenging but important, because there are different treatment outcomes. Methods: We report 3 patients with A-CIDP who were initially diagnosed with severe GBS but were later confirmed to have CIDP based on their clinical course and electrodiagnostic (EDx) studies. We also report on the long-term treatment of these patients and review the literature on EDx studies in this syndrome. Results: Three patients were initially diagnosed with GBS and responded to treatment. However, all 3 had arrest in improvement or deterioration during their rehabilitation phases. EDx studies showed prominent demyelinating changes many months after the initial presentation. All responded very well to immunotherapy. Conclusion: Although several features may suggest the diagnosis of A-CIDP at initial presentation, close follow-up of GBS patients during the recovery phase is also needed for accurate diagnosis. EDx studies may distinguish patients with A-CIDP from GBS patients.
机译:急性发作的慢性炎性脱髓鞘性多发性神经病(A-CIDP)是一种日益被认可的CIDP亚型。将A-CIDP与格林巴利综合征(GBS)区别开来具有挑战性,但很重要,因为治疗结果不同。方法:我们报告了3名A-CIDP患者,他们最初被诊断出患有严重的GBS,但随后根据其临床病程和电诊断(EDx)研究被确认患有CIDP。我们还报告了这些患者的长期治疗,并回顾了有关该综合征的EDx研究文献。结果:3例患者最初被诊断出患有GBS并且对治疗有反应。但是,这三人在康复阶段都因改善或恶化而被捕。 EDx研究显示,初次出现后许多月,脱髓鞘发生了显着变化。所有人对免疫疗法的反应都很好。结论:尽管有几项特征可能提示在初次就诊时可诊断为A-CIDP,但准确诊断GBS患者在恢复期也需要密切随访。 EDx研究可将A-CIDP患者与GBS患者区分开。

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