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Intravenous immunoglobulins (IVIG) as long-term therapy in general myasthenia gravis: A case series

A Wellek, C Eienbröker, B von Hagen, WH Oertel, N Sommer, B Tackenberg · Klinische Neurophysiologie · 2008 · Heft 04

Dokument
973688
CareLit-ID
Jahr
2008
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Neurophysiologie
Autor:innen
A Wellek, C Eienbröker, B von Hagen, WH Oertel, N Sommer, B Tackenberg
Ausgabe
Heft 04 / 2008
Seiten
–
Erschienen: 2008-04-08 00:00:00
ISSN
1434-0275

Zusammenfassung

Introduction: Myasthenia gravis (MG) is an autoimmune disease caused by autoantibodies against acetylcholine receptors at the neuromuscular junction. Steroids and azathioprin are established for long-term immunosuppressive treatment. In cases of failed efficacy other immunosuppressive drugs, like ciclosporine, metho-trexate or mycophenolate can be used. Additionally, IVIG is accepted to be administered in myasthenic crisis or acute exacerbation of motor function without respiratory insufficiency, but not as „add-on“ long-term treatment. Nevertheless, myasthenia gravis symptoms are not always stable under immunos…

Schlagworte

Klinische Neurophysiologie