Myopericarditis in giant cell arteritis: case report of diagnostic dilemma and review of literature
- 1Department of Rheumatology, Countess of Chester hospital, Chester, UK
- 2Department of Cardiology, Countess of Chester NHS Trust, Chester, UK
- Correspondence to Professor John D Somauroo,
Giant cell arteritis (GCA), also known as granulomatous arteritis is a systemic vasculitis mainly affecting extra cranial branches of carotid arteries. It can rarely affect other vascular beds causing thoracic aorta aneurysm, dissection and rarely cause myocardial infarction through coronary arteritis. It can cause considerable diagnostic dilemma due to varied clinical presentations. The authors report an illustrative case of a 70-year-old woman with GCA who developed symptoms suggestive of acute myocardial infarction with chest pain, localised ST-T changes and echocardiographic left ventricular dysfunction. However, cardiac troponin T biomarkers and coronary angiography were normal. Her symptoms subsided with steroid treatment. Cardiac symptoms at first presentation of GCA are unusual.
Competing interests None.
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