A Case Series of unusual presentations of Immune-Mediated Polymyositis
DOI:
https://doi.org/10.48047/e9p4s488Keywords:
.Abstract
Idiopathic inflammatory myopathies involve four major subtypes that include: Polymyositis, Dermatomyositis,
Inclusion Body Myositis and Necrotizing myopathy. Polymyositis is an autoimmune and chronic inflammatory
disease characterized by symmetrical proximal muscle weakness due to the involvement of endomysial layers
and skeletal muscles.
Polymyositis develops due to abnormal activation of cytotoxic T lymphocytes (CD8 cells) and macrophages
against muscular antigens.
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