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Pathologic Features of Anti-Ku Myositis.

Munenori OyamaMarie-Therese HolzerYuko OhnukiYoshihiko SaitoYukako NishimoriShingo SuzukiTakashi ShiinaSarah Leonard-LouisOlivier BenvenisteUdo SchneiderWerner StenzelIchizo NishinoShigeaki SuzukiAkinori Uruha
Published in: Neurology (2024)
While anti-Ku myositis shows necrotizing myopathy features, they can be distinguished from anti-SRP/HMGCR IMNM by their MHC class II expression and clusters of perivascular inflammatory cells. The HLA analyses suggest that anti-Ku myositis may have different subsets associated with myopathologic subgroups.
Keyphrases
  • induced apoptosis
  • neoadjuvant chemotherapy
  • late onset
  • radiation therapy
  • locally advanced
  • duchenne muscular dystrophy