Medical Journal of Dr. D.Y. Patil Vidyapeeth (Sep 2024)

MuSK Antibody Positive Myasthenia Gravis Mimicking as Myositis

  • Nilesh Wagh,
  • Ajit P. Mishra,
  • Srikant K. Sahoo,
  • Lulup K. Sahoo,
  • Tanaya Mishra

DOI
https://doi.org/10.4103/mjdrdypu.mjdrdypu_380_23
Journal volume & issue
Vol. 17, no. 5
pp. 1072 – 1074

Abstract

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Most common neuromuscular junction disorder is Myasthenia gravis (MG) which has variable clinical presentations. Diplopia and drooping of eyelids are the peculiarity of myasthenia gravis. Commonly disease manifests as a fluctuating weakness of skeletal muscles. Although respiratory symptoms may be the initial presenting complaint in a few patients, usually it develops during the later part of the disease course. The initial presentation of isolated prominent respiratory distress is a relatively rare presentation of myasthenia gravis unless accompanied by other clinical features. We report a 40-year-old female patient, who visited our hospital with presenting complaints of breathlessness and generalized myalgia and subsequently developed fatigable weakness during hospitalization.

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