Head and neck giant cell arteritis: an autoimmune disease with many faces
Markus Wirth1, Lucas Schirmer2, Benedikt Hofauer1
1a Department of Otolaryngology - Head and Neck Surgery , Klinikum rechts der Isar, Technical University of Munich , Munich , Germany.
Insights
Giant cell arteritis (GCA) can present atypically in the head and neck, particularly with odynophagia and elevated CRP. Consider GCA in elderly patients with these symptoms to avoid diagnostic delays.
Area of Science:
- Otolaryngology
- Rheumatology
- Internal Medicine
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis primarily affecting large and medium-sized arteries.
- Head and neck manifestations of GCA can be diverse, sometimes presenting atypically.
Purpose of the Study:
- To characterize the clinical presentation of head and neck GCA.
- To develop a diagnostic pathway for atypical GCA cases presenting to an ENT department.
Main Methods:
- Retrospective analysis of 65 patients diagnosed with head and neck GCA between 2002 and 2012.
- Focus on manifestations encountered in the otolaryngology, ophthalmology, and neurology departments.
Main Results:
- Vision loss (83%) and new-onset headache (63%) were the most common symptoms.
- Eight patients (12%) had infrequent presentations, with odynophagia and elevated CRP being the most common atypical sign, often mistaken for infection.
- A diagnostic pathway was formulated using ACR criteria and clinical findings.
Conclusions:
- Infrequent presentations of GCA are common in ENT departments.
- Odynophagia with elevated CRP in older patients warrants consideration for GCA, even without typical findings.
- Anticipating GCA as a differential diagnosis in such cases is crucial for timely management.
Conclusion:
A high rate of infrequent presentations of giant cell arteritis were seen in the ENT department and should be anticipated as a differential diagnosis in every older patient with odynophagia with high CRP values without cause in thorough ENT examination.
Objective:
To describe the clinical manifestation of head and neck giant cell arteritis and to derive a diagnostic pathway covering atypical cases.
Method:
Single-center, retrospective analysis of cases with GCA in the head and neck region (HN-GCA) (2002-2012) to describe the clinical presentation and to derive a diagnostic pathway covering manifestations presenting to an ENT department.
Results:
Sixty-five patients were newly diagnosed with HN-GCA in the department of otolaryngology, ophthalmology and neurology. The most frequent symptoms were loss of vision (83%) and new onset headache (63%). Eight patients (12%) presented with infrequent manifestations, predominantly in the department of otorhinolaryngology. The most common atypical presentation (50%) was odynophagia in conjunction with high CRP values misleading to an infectious cause and delaying diagnosis. A diagnostic pathway for GCA was derived based on the ACR classification criteria and the clinical findings.
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