Rambam Maimonides Medical Journal (Oct 2022)

A Unique Case of Myositis

  • Noa Hurvitz,
  • Ariel Kenig,
  • Asa Kessler,
  • Narmine Elkhateeb,
  • Yossef Lerner,
  • Michal Zamir,
  • Fadi Kharouf

DOI
https://doi.org/10.5041/RMMJ.10481
Journal volume & issue
Vol. 13, no. 4
p. e0030

Abstract

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Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a rare systemic small-vessel disease, with heterogeneous clinical manifestations. While arthralgia and myalgia are common in the disease course, frank myositis is exceedingly rare. Immune-mediated necrotizing myopathy (IMNM) is a subtype of idiopathic inflammatory myopathies (IIMs), characterized by severe myositis. We report herein a case of prominent diffuse myositis with shared features of AAV and IMNM.

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