A case of severe chronic inflammatory demyelinating polyradiculoneuropathy with monoclonal gammopathy of undetermined significance with alternating immunoglobulin class to IgM from IgA
Author:
Affiliation:
1. Department of Neurology, Gunma University Graduate School of Medicine
2. Gunma Rehabilitation Hospital
3. Department of Neurology, Kinki University School of Medicine
4. Geriatrics Research Institute and Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/56/9/56_cn-000889/_pdf
Reference24 articles.
1. 1) Hadden RDM, Nobile-Orazio E, Sommer C, et al. European Federation of Societies/Peripheral Nerve Society guideline on management of paraproteinaemic demyelinating neuropathies: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society. Eur J Neurol 2006;13:809-818.
2. 2) Bromberg MB, Feldman EL, Albers JW. Chronic inflammatory demyelinating polyradiculoneuropathy: comparison of patients with and without an associated monoclonal gammopathy. Neurology 1992;42:1157-1163.
3. 3) Simmons Z, Albers JW, Bromberg MB, et al. Presentation and initial clinical course in patients with chronic inflammatory demyelinating polyradiculoneuropathy: comparison of patients without and with monoclonal gammopathy. Neurology 1993;43:2202-2209.
4. 4) Mehndiratta MM, Sen K, Tatke M, et al. IgA monoclonal gammopathy of undetermined significance with peripheral neuropathy. J Neurol Sci 2004;221:99-104.
5. 5) Bailey RO, Ritaccio AL, Bishop MB, et al. Benign monoclonal IgAK gammopathy associated with polyneuropathy and dysautonomia. Acta Neurol Scand 1986;73:574-580.
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1. Chronic Inflammatory Demyelinating Polyradiculoneuropathy in Association With Concomitant Diseases: Identification and Management;Frontiers in Immunology;2022-07-04
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