Coexistence of anti-MuSK antibody-positive myasthenia gravis and rheumatoid arthritis

A Eker, M Tınazlı, SE Mut - The Egyptian Journal of Neurology, Psychiatry …, 2020 - Springer
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020Springer
Background Rheumatoid arthritis (RA) is an autoimmune disease characterized with
symmetric synovitis and occasional extra articular involvement; also, some neurologic
disorders can be observed during the disease course. Myasthenia gravis (MG) is one of
them and it is an autoimmune disease of neuromuscular junction. It is caused by
autoantibodies against neuromuscular junction proteins: the nicotinic acetylcholine receptor
(AChR) and the muscle specific tyrosine kinase (MuSK). Very few studies have reported the …
Background
Rheumatoid arthritis (RA) is an autoimmune disease characterized with symmetric synovitis and occasional extra articular involvement; also, some neurologic disorders can be observed during the disease course. Myasthenia gravis (MG) is one of them and it is an autoimmune disease of neuromuscular junction. It is caused by autoantibodies against neuromuscular junction proteins: the nicotinic acetylcholine receptor (AChR) and the muscle specific tyrosine kinase (MuSK). Very few studies have reported the associated autoimmune disorders in MuSK-MG. Here, we present the first patient who has MuSK antibody-positive MG gravis and rheumatoid arthritis.
Case presentation
A 53-year-old woman with RA presented with fatigue and fluctuating proximal muscle weakness. Her electroneurophysiological investigation resembled MG. Her AchR antibody level was normal but MuSK antibodies were high. After the acute treatment with plasmapheresis which lead to complete recovery in myasthenic symptoms, she is following with mycophenolate mofetil.
Conclusions
Concomitant autoimmune disorders are common in the population. MG should be considered in patients with an autoimmune disorder and developing new neuromuscular weakness.
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