Literature DB >> 1323757

Demyelinating polyneuropathy in eosinophilia-myalgia syndrome.

P D Donofrio1, C Stanton, V S Miller, L Oestreich, D S Lefkowitz, F O Walker, E W Ely.   

Abstract

Eosinophilia-myalgia syndrome (EMS) is a newly recognized disorder, characterized by myalgia, weakness, scleroderma-like changes, and eosinophilia. EMS is associated with lots of L-tryptophan allegedly contaminated with byproducts of the manufacturing process. We describe 3 patients with EMS who presented with a severe demyelinating sensorimotor polyneuropathy. Electrodiagnostic studies revealed multifocal conduction block, slowing and temporal dispersion of motor responses, and prolonged or absent F-responses. Despite plasmapheresis; corticosteroids; and, in 1 patient, cyclophosphamide, 2 patients died and the remaining patient experienced minimal recovery. Pathology revealed patchy perivascular infiltrates and fibrosis in the connective tissue of muscle and nerve. Autopsy of the central nervous system in 2 patients did not reveal changes unique to EMS. In addition to other organ involvement, EMS may manifest as a potentially fatal polyneuropathy, which initially appears to have prominent demyelinating features.

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Year:  1992        PMID: 1323757     DOI: 10.1002/mus.880150708

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  3 in total

1.  Two cases of neurological manifestations in eosinophilia: variations of one disease?

Authors:  S Ostrowitzki; S Zierz
Journal:  Clin Investig       Date:  1994-12

Review 2.  Toxic myopathies.

Authors:  Mamatha Pasnoor; Richard J Barohn; Mazen M Dimachkie
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

3.  Pediatric sciatic neuropathy presenting as painful leg: A case report and review of literature.

Authors:  Manish Prasad; Mohamed Babiker; Ganesh Rao; Christopher Rittey
Journal:  J Pediatr Neurosci       Date:  2013-05
  3 in total

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