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Updated: May 27, 2026

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Heart transplantation following myocardial infarction due to Takayasu's arteritis
Angela McBrien1, Massimo Griselli, Mark Friswell
1Department of Paediatric Cardiology, Freeman Hospital, Newcastle upon Tyne, UK. angmcb@yahoo.co.uk
Insights
A young girl with Takayasu's arteritis developed cardiogenic shock due to coronary artery compression. She successfully underwent cardiac transplantation, a procedure not previously reported for this condition.
Area of Science:
- Cardiology
- Vascular Surgery
- Rheumatology
Background:
- Takayasu's arteritis is a rare, large-vessel vasculitis.
- It can affect the aorta and its branches, including coronary arteries.
- Complications can lead to severe cardiac dysfunction.
Observation:
- A 14-year-old female presented with cardiogenic shock.
- Coronary artery compression, specifically the left main coronary artery, was identified as the cause.
- Ascending aortitis was also present, necessitating extensive surgical intervention.
Findings:
- The patient required emergent cardiac transplantation.
- A hemi-arch replacement was performed concurrently with the transplant.
- This represents the first reported case of cardiac transplantation for Takayasu's arteritis.
Implications:
- Cardiac transplantation is a viable option for managing life-threatening cardiac complications of Takayasu's arteritis.
- Early diagnosis and intervention are crucial in pediatric cases.
- This case expands treatment options for severe Takayasu's arteritis.
Abstract:
We report a 14-yr-old girl who presented with cardiogenic shock because of compression of the left main coronary artery secondary to Takayasu's arteritis. The patient required cardiac transplantation with hemi-arch replacement at the time of transplant because of ascending aortitis. To our knowledge, this is the first case of cardiac transplantation in Takayasu's arteritis to be reported in the literature.
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