Polymyositis and dermatomyositis diagnostic study of choice
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Differentiating Polymyositis and dermatomyositis from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]
Overview
Diagnostic Study of Choice
- Muscle biopsy is the gold standard test for the diagnosis of polymyositis and dermatomyositis.[1]
- The following result of muscle biopsy is confirmatory of polymyositis and dermatomyositis:
- Necrosis
- Phagocytosis
- Regenerative activity reflected by basophilia, large, vesicular nuclei and prominent nucleoli
- Atrophy and degeneration of both Type I and II fibers, especially in a perifascicular distribution
- Internal migration of nuclei
- Vacuolization
- Fiber-size variation
- Mononuclear inflammatory infiltrate, often most prominent in a perivascular location
- Increase in endomysial and perimysial connective tissue
- The muscle biopsy should be performed when:
- The patient presented with symptoms of muscle weakness and skin rash
- An elevated level of muscle enzymes is detected in the patient.
References
- ↑ Bohan, Anthony; Peter, James B. (1975). "Polymyositis and Dermatomyositis". New England Journal of Medicine. 292 (8): 403–407. doi:10.1056/NEJM197502202920807. ISSN 0028-4793.