Childhood CIDP: Study of 31 patients and comparison between slow and rapid-onset groups

被引:14
作者
Cabasson, Sebastien [1 ]
Tardieu, Marc [2 ]
Meunier, Ariane [3 ]
Rouanet-Larriviere, Marie-France [4 ]
Boulay, Christophe [5 ]
Pedespan, Jean-Michel [1 ]
机构
[1] CHU Bordeaux, Hop Pellegrin Enfants, Unite Neurol Enfant & Adolescent, F-33076 Bordeaux, France
[2] Univ Paris Sud, Assistance Publ Hop Paris, Serv Neurol Pediat, F-94275 Le Kremlin Bicetre, France
[3] CHU Strasbourg, Serv Neurol Pediat, Strasbourg, France
[4] CHU Bordeaux, Unite Neurophysiol, Bordeaux, France
[5] Assistance Publ Hopitaux Marseille, Unite Neurophysiol, Marseille, France
关键词
Acquired neuropathy; Inflammatory diseases; Guillain-Barre; Intravenous immunoglobulins; Corticosteroids; INFLAMMATORY DEMYELINATING POLYNEUROPATHY; CLINICAL-COURSE; POLYRADICULONEUROPATHY; PREVALENCE; CHILDREN;
D O I
10.1016/j.braindev.2015.04.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To describe 31 children presenting a CIDP; to compare patients with rapid-onset disease vs. patients with slow-onset disease, a rapid-onset disease being defined by a time to peak impairment of less than 8 weeks. Study design: A retrospective chart review identified 31 patients completing criteria for childhood CIDP, with 24 "confirmed CIDP" and 7 "possible CIDP". Data collected were time to peak impairment, clinical presentation, cerebrospinal fluid analysis, nerve conduction study, nerve biopsy, treatments. Evaluation at the end of follow-up was reported according to modified Rankin scale. Results: Thirteen patients (42%) exhibited symptoms in less than 2 months with more often cranial nerve abnormalities (38% vs. 6%, p = 0.059), and sensitive symptoms (62% vs. 11%, p = 0.0057). They evolved predominantly in a relapsing way (69% vs. 22%, p = 0.0047). Length of the disease was also longer in the rapid-onset group (5.5 years vs. 3.83 years) but without statistical difference. The slow-onset group exhibited more frequently ataxia at onset (28% vs. 8%, p > 0.05), and evolved predominantly in a progressive manner (61% vs. 15%, p > 0.05). Outcome was similar and good in the two groups. At least 3 out of the 4 major electrophysiological criteria were positive for 27/31 children (87%). Axonal involvement could be present very early. Immunoglobulins were given in 29 cases and corticosteroids in 22. A partial or complete recovery 1 month after first treatment was reported in 30 cases. Among second-line treatments, only azathioprine seemed effective in two out of three intractable Children. Conclusions: The differences noted between the two groups should be tested in wider populations. Electrophysiological criteria are restrictive and axonal involvement should be studied. Prospective trials are required to find out the best first and second line treatments. (C) 2015 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:943 / 951
页数:9
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