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Familial Mediterranean Fever Complicated By Massive Cardiac Tamponade
Lara Melo1, Haris Patail1, Garima Gautam1
1Internal Medicine, University of Connecticut Health, Farmington, USA.
Abstract:
Familial Mediterranean fever (FMF) is a hereditary, autosomal recessive auto-inflammatory disorder characterized by recurrent attacks of fever and serositis. While arthritis, pleuritis, peritonitis, and pericarditis are common in FMF, large pericardial effusions with cardiac tamponade as a sequelae of FMF are considered rare. We report a case of an 83-year-old female with a history of FMF who presented with chest pain. She was found to have acute pericarditis complicated by hemodynamically significant pericardial tamponade that was subsequently treated with an urgent pericardiocentesis followed by colchicine.
Insights
Familial Mediterranean fever (FMF) can rarely cause large pericardial effusions leading to cardiac tamponade. This case highlights the importance of considering FMF in patients presenting with these rare but serious cardiovascular complications.
Area of Science:
- Internal Medicine
- Cardiology
- Rheumatology
Background:
- Familial Mediterranean fever (FMF) is an inherited autoinflammatory disease.
- FMF commonly presents with fever and serositis, including pericarditis.
- Large pericardial effusions and cardiac tamponade are rare complications of FMF.
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