Drug-induced myasthenic syndromes

نویسنده

  • Thomas Klopstock
چکیده

Drug-induced myasthenic syndromes are caused by numerous medications of various classes. D-penicillamine and interferon alpha lead to an autoimmune process similar to spontaneous myasthenia gravis, whereas many other agents produce weakness by a direct compromise of neuromuscular transmission. A particular problem in clinical practice is the deterioration of neuromuscular transmission by anesthetics and neuromuscular blocking drugs. Moreover, novel drugs may show myasthenia-like syndromes or exacerbation of preexisting myasthenia gravis during clinical studies or in post-marketing surveillance. In this article, the author draws attention to the rare occurrence of drug-induced myasthenia with a new class of anticancer drugs, the immune checkpoint inhibitors. These include the drug ipilimumab targeting cytotoxic lymphocyte-associated protein 4 (CTLA-4), and the drugs nivolumab and pembrolizumab targeting programmed cell death-1 (PD-1). Management of drug-induced myasthenia in these cases requires withdrawal of the immune checkpoint inhibitor and standard immunotherapy including high-dose steroids.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Congenital Myasthenic Syndromes with Predominant Limb Girdle Weakness

Congenital myasthenic syndromes are a heterogeneous group of genetically determined disorders characterized by impaired neuromuscular transmission. They usually present from birth to childhood and are characterised by exercise induced weakness and fatigability. Genotype-phenotype correlations are difficult. However, in some patients particular phenotypic aspects may point towards a specific gen...

متن کامل

A Case Report of Congenital Myasthenia Gravis Presenting With Respiratory Distress

Congenital Myasthenic Syndromes (CMS) are rare inherited disorders characterized by dysfunction of neuromuscular transmission at the neuromuscular junction. Most patients with congenital myasthenic syndromes present in the infancy. Major symptoms of affected individuals include weakness and fatigue during the first years of life. Patients may show hypotonia, facial weakness, swallowing difficul...

متن کامل

Defective N-linked protein glycosylation pathway in congenital myasthenic syndromes.

Original Articles Rhythm-specific modulation of the sensorimotor network in drug-naı̈ve patients with Parkinson’s disease by levodopa F. Esposito, A. Tessitore, A. Giordano, R. De Micco, A. Paccone, R. Conforti, G. Pignataro, L. Annunziato and G. Tedeschi 710 Evidence for adaptive cortical changes in swallowing in Parkinson’s disease S. Suntrup, I. Teismann, J. Bejer, I. Suttrup, M. Winkels, D. ...

متن کامل

Congenital myasthenic syndromes.

PURPOSE OF REVIEW Congenital myasthenic syndromes are a heterogeneous group of diseases caused by genetic defects affecting neuromuscular transmission. In this article, a strategy that leads to the diagnosis of congenital myasthenic syndromes is presented, and recent advances in the clinical, genetic and molecular aspects of congenital myasthenic syndrome are outlined. RECENT FINDINGS Besides...

متن کامل

Congenital myasthenic syndromes.

Congenital myasthenic syndromes are a rare group of heterogeneous disorders affecting neuromuscular transmission. Recent identification and in-vitro functional analysis of some of the genetic mutations that cause these disorders correlates with previous electrophysiological, biochemical, pathological and therapeutic studies, and has advanced our understanding of neuromuscular transmission.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017