医学
慢性炎症性脱髓鞘性多发性神经病
不确定意义的单克隆抗体病
内科学
多神经根神经病
糖尿病
多发性神经病
疾病
单克隆抗体病
胃肠病学
免疫学
单克隆
抗体
单克隆抗体
格林-巴利综合征
内分泌学
作者
S. Jann,Sandro Beretta,Manuela A. Bramerio
摘要
Abstract Chronic inflammatory demyelinating polyneuropathy (CIDP) can occur in association with other systemic diseases such as diabetes mellitus (DM) and IgG or IgA monoclonal gammopathy of undetermined significance (MGUS). Whether CIDP that is idiopathic (I‐CIDP) or associated with diabetes (CIDP‐DM) or MGUS (CIDP‐MGUS) differ in clinical presentation, laboratory features, response to treatment, and long‐term outcome is unclear, as is the relationship between these coexisting diseases and CIDP. In order to clarify this issue, we began a prospective follow‐up study. Thirty‐one consecutive patients with untreated CIDP, fulfilling the most restrictive diagnostic criteria, were enrolled over 18 months. Among the patients, 16 were diabetic, 7 had a MGUS, and 8 had an idiopathic CIDP. All patients were treated with IVIg, and the responders were treated again if they relapsed. In all three groups, improvement occurred after treatment. At the end of the follow‐up, there was no difference in clinical conditions between groups, but a significant difference existed in the number of relapses and of IVIg administrations. CIDP‐DM is a more severe disease, but with a significantly better response to IVIg and fewer relapses, than the other types that we studied. Muscle Nerve, 2005
科研通智能强力驱动
Strongly Powered by AbleSci AI