An Unusual Presentation of Dysphagia in a Young Male with Myositis

  • Jaisy James Aster Medcity, Kochi
  • PS Shahanas Aster Medcity, Kochi.
  • Geetha Mary Philips Aster Medcity, Kochi
  • Joe Thomas Aster Medcity, Kochi
  • Aysha Sana Aster Medcity, Kochi
  • Merin M Ittiachen Aster Medcity, Kochi
  • Niranjana Chandran Aster Medcity, Kochi
Keywords: Dysphagia, Myositis, Inflammation

Abstract

Dysphagia is a rare presentation in patients with viral myositis and only 10%-20% of patients with myositis developed weakness of oropharyngeal, laryngeal, and oesophageal musculature that leads to impairment in the oropharyngeal phase of swallowing. The proper mechanism of dysphagia in patients with myositis remains unclear and it is thought to be due to impaired muscle contractions and decreased hyo-laryngeal excursion that leads to impaired relaxation of the upper oesophageal sphincter. Delayed treatment, bulbar involvement, respiratory involvement, old age, and occurrence of malignancy are associated with poor prognosis. Here we are describing a case of a 25-year-old gentleman who presented with fever, myalgia, and dark-colored urine, who was diagnosed as viral myositis with dysphagia, and a holistic approach in the management of the disease.

Author Biographies

Jaisy James, Aster Medcity, Kochi

Department of Internal Medicine

PS Shahanas, Aster Medcity, Kochi.

Department of Internal Medicine

Geetha Mary Philips, Aster Medcity, Kochi

Department of Internal Medicine

Joe Thomas, Aster Medcity, Kochi

 Department of Rheumatology

Aysha Sana, Aster Medcity, Kochi

Department of Clinical Pharmacy

Merin M Ittiachen, Aster Medcity, Kochi

Department of ENT

Niranjana Chandran, Aster Medcity, Kochi

Department of ENT

Published
2024-12-30
How to Cite
James, J., Shahanas, P., Philips, G., Thomas, J., Sana, A., Ittiachen, M., & Chandran, N. (2024). An Unusual Presentation of Dysphagia in a Young Male with Myositis. Kerala Medical Journal, 17(4), 216-219. https://doi.org/10.52314/kmj.2024.v17i4.682
Section
Case Series / Case Report