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Patient with Takayasu arteritis presented as cardiogenic shock
Gulten Tacoy1, Ahmet Akyel, Yusuf Tavil
1Gazi University Faculty of Medicine, Cardiology Department, Besevler, Ankara, Turkey. gtacoy@gmail.com
Takayasu arteritis, a rare inflammatory disease, can present with cardiogenic shock. This case highlights a 47-year-old male with initial cardiogenic shock due to extensive aortic and branch artery occlusion.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Vascular Inflammation
Background:
- Takayasu arteritis is a chronic inflammatory vasculitis affecting the aorta and its branches.
- It predominantly impacts young women, with cardiac complications being uncommon.
- Coronary artery disease and cardiogenic shock are particularly rare initial manifestations.
Observation:
- A 47-year-old male presented with severe cardiogenic shock.
- Initial investigations revealed extensive arterial occlusive disease.
- The patient had no prior history suggestive of Takayasu arteritis.
Findings:
- The patient was diagnosed with Takayasu arteritis.
- The disease caused occlusion of the coronary arteries, subclavian artery, celiac artery, and the entire abdominal aorta.
- Cardiogenic shock was the presenting symptom, a rare initial sign.
Implications:
- This case underscores that Takayasu arteritis can present atypically in men.
- It emphasizes the importance of considering Takayasu arteritis in patients with unexplained cardiogenic shock and extensive vascular occlusion.
- Early diagnosis and management are crucial to prevent severe cardiovascular events.
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