Key result
Aortic homograft successfully relieves recurrent complex supravalvular and valvular aortic stenosis after repeated reoperations.
Why the study?
Supravalvular aortic stenosis is a rare congenital anomaly with progressive nature that may require repetitive surgical interventions in certain cases with risk factors.
Case Report (n=1)
No
Patients with supravalvular aortic stenosis may require repetitive surgical interventions due to disease progression, highlighting the need for lifelong close follow-up.
Case of progressive supravalvular stenosis requiring serial reoperations underscores need for close surveillance; leaves open optimal timing and strategies in this rare subset.
Supravalvular aortic stenosis, which is a rare congenital cardiac anomaly, is associated with several lesions and has a progressive nature. Herein, we report a five-year-old girl with bicuspid aorta who underwent initial Doty operation at the age of nine months. A combined redo Doty operation and an aortic valve commissurotomy were performed two years later. Due to the rapidly progressing aortic regurgitation and both valvular and supravalvular gradient, a repeated surgery was required at the age of five years and an aortic homograft was successfully inserted with an annulus enlargement and the patient was discharged uneventfully. In conclusion, although Doty repair yields satisfactory results in most patients, certain cases with identified risk factors may require reoperations due to the progressive nature of the disease. Therefore, these patients should be kept under a close follow-up lifelong.
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Gökmen Akkaya (2019) conducted a case report in Supravalvular aortic stenosis (n=1). Doty operation and aortic homograft insertion was evaluated on Relief of supravalvular and valvular gradient. A five-year-old girl with supravalvular aortic stenosis and a bicuspid aortic valve required multiple reoperations, ultimately undergoing successful aortic homograft insertion to relieve progressive stenosis and regurgitation.
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