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Rare forms of inflammatory myopathies - part II, localized forms
Claudio Galluzzo1, Ilaria Chiapparoli1, Ada Corrado2
1Department of Internal Medicine, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Expert Review of Clinical Immunology
|December 5, 2022
Summary
This review covers rare, localized forms of idiopathic inflammatory myopathies, often misdiagnosed as tumors. Understanding these uncommon myositis presentations is key for accurate diagnosis and treatment.
Area of Science:
- Neurology
- Rheumatology
- Immunology
Background:
- Idiopathic inflammatory myopathies (IIMs) traditionally include dermatomyositis, polymyositis, anti-synthetase syndromes, immune-mediated necrotizing myopathy, and inclusion body myositis.
- Uncommon localized forms of IIMs are less recognized and can be challenging to diagnose.
Conclusions:
- Increased awareness of rare localized myositis is crucial for timely diagnosis.
- Knowledge of these conditions facilitates appropriate management and improves patient outcomes.
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