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Published on: February 8, 2019
Giant cell arteritis: Diagnostic approach based on a retrospective study on 21 cases
Haifa Tounsi1, Jaafer Aouni2, Ghada Kharrat3
1Department of Internal Medicine, Mohamed Tahar Maamouri University Hospital, Nabeul 8000, Tunisia.
Giant cell arteritis (GCA) management presents diagnostic and therapeutic challenges. Early consultation is crucial to prevent irreversible sight loss and stroke, despite its rarity in Tunisia.
Area of Science:
- Rheumatology
- Internal Medicine
- Ophthalmology
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis affecting large and medium arteries.
- Early diagnosis and treatment are vital to prevent severe complications such as vision loss and stroke.
Purpose of the Study:
- To outline the diagnostic and therapeutic challenges in managing giant cell arteritis (GCA).
- To highlight the importance of timely intervention in GCA cases.
Main Methods:
- Retrospective study of 21 GCA patients diagnosed using 1990 ACR criteria.
- Data collected over a 5-year period (2014-2019) at Mohamed Tahar Maamouri Hospital, Tunisia.
- Review of clinical presentation, diagnostic workup (biopsy, imaging), treatment, and outcomes.
Main Results:
- Headache and ocular manifestations were the most common presenting symptoms.
- Temporal artery biopsy confirmed diagnosis in 9 cases; imaging revealed aortitis/ectasia in 2 cases.
- Corticosteroids were primary treatment; adverse effects included osteoporosis and diabetes. Two patients experienced irreversible blindness due to delayed consultation.
Conclusions:
- Giant cell arteritis (GCA) requires prompt management due to risks of sight loss and stroke.
- Despite rarity in Tunisia, GCA is a medical emergency demanding swift diagnosis and treatment.
- Adherence to diagnostic criteria and prompt initiation of therapy are essential for favorable outcomes.
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