Diagnostic Approach to Polymyalgia Rheumatica (PMR)
The diagnostic approach to polymyalgia rheumatica requires a combination of clinical assessment, laboratory testing, and exclusion of mimicking conditions, with ESR and CRP being essential inflammatory markers to support the diagnosis. 1, 2
Clinical Features to Assess
- Bilateral shoulder pain with morning stiffness lasting >45 minutes in patients >50 years old is the hallmark presentation 1, 3
- Functional impairment of the shoulder girdle with pain on movement 1, 4
- Pelvic girdle pain and stiffness (though not mandatory for diagnosis) 2, 5
- Constitutional symptoms including fatigue, low-grade fever, and weight loss may be present 4, 5
- Rapid onset of symptoms, developing over days to weeks 5
Core Laboratory Workup
Essential inflammatory markers:
Autoantibody testing:
Basic laboratory panel:
Additional Recommended Tests
- Protein electrophoresis to exclude paraproteinemia 1
- Thyroid stimulating hormone (TSH) to rule out thyroid disorders 1
- Creatine kinase to exclude myopathies and myositis 1, 4
- Vitamin D level as baseline before potential glucocorticoid therapy 1
Extended Testing Based on Clinical Presentation
- Anti-nuclear antibodies (ANA) and anti-cytoplasmic neutrophil antibodies (ANCA) when other autoimmune conditions are suspected 1
- Tuberculosis testing when immunosuppressive therapy is being considered 1
- Chest radiograph to exclude malignancy 1
Imaging Studies
- Ultrasound can detect bilateral subdeltoid bursitis in 69% of PMR patients 3
- MRI may reveal inflammation in proximal joints and periarticular structures 7
- Consider advanced imaging (ultrasound, MRI, PET-CT) in atypical presentations 5
Diagnostic Algorithm
Initial assessment:
Differential diagnosis:
Therapeutic trial:
Special Considerations
Consider specialist referral for atypical presentations including:
Always consider giant cell arteritis (GCA) in PMR patients who develop:
Common Pitfalls and Caveats
- No single test is pathognomonic for PMR; diagnosis remains primarily clinical 1
- PMR with normal inflammatory markers is rare but possible and warrants specialist evaluation 6
- Failure to respond to moderate-dose glucocorticoids should prompt reconsideration of diagnosis 2, 4
- Overlooking giant cell arteritis can lead to irreversible vision loss 3, 4
- PMR-like syndromes may develop as a side effect of cancer treatment with checkpoint inhibitors 5