This 27-year-old female patient is undergoing a reoperation for a recurrent subaortic membrane causing significant left ventricular outflow obstruction. The re-sternotomy is uneventful and cardiopulmonary bypass is established. The left ventricular outflow tract is accessed through the previously implanted semi-calcified homograft aortic root. The fibrous tissue of the subaortic membrane is resected as a crescent, along with a septal myectomy. The aortic annulus and previous aortic homograft are resected to enlarge the aortic root from 12 mm to 21 mm. The left ventricular outflow tract is then reconstructed with pericardium, and a valved conduit aortic root replacement, size 21 mm Konect prosthesis, is implanted. The pericardium is closed with Gore-Tex membrane, should future surgery be needed. A 21-mm valve was considered adequate, given her height of 157 cm and low body surface area of 1.45 m2. This patient was not an appropriate candidate for a Ross-Konno procedure or a mechanical valve due to extremely challenging social circumstances, medical noncompliance and housing insecurity.
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http://dx.doi.org/10.1510/mmcts.2025.004 | DOI Listing |
Multimed Man Cardiothorac Surg
March 2025
Northwell Cardiovascular Institute, New York, NY, USA.
This 27-year-old female patient is undergoing a reoperation for a recurrent subaortic membrane causing significant left ventricular outflow obstruction. The re-sternotomy is uneventful and cardiopulmonary bypass is established. The left ventricular outflow tract is accessed through the previously implanted semi-calcified homograft aortic root.
View Article and Find Full Text PDFEur Heart J Case Rep
March 2025
Department of Cardiovascular Surgery, Ayase Heart Hospital, 2-16-7 Yanaka, Adachi-Ku, Tokyo 120-0006, Japan.
Background: We report a rare case of trans-catheter aortic valve implantation (TAVI) in an elderly male with membranous ventricular septal defect (VSD), sub-aortic band, and severe aortic stenosis (AS). We discuss the safety and efficacy of the technique.
Case Summary: An 86-year-old male was admitted to our hospital with congestive heart failure due to low-flow low-gradient severe AS, a membranous VSD, a sub-aortic band, and a double-chambered right ventricle (RV).
J Surg Case Rep
February 2025
Faculty of Medicine, Damascus University, Damascus, Syria.
Subaortic stenosis (SAS) is a rare congenital heart defect (CHD), accounting for 1%-2% of all CHD and the second most common type of left ventricular outflow tract (LVOT) obstruction. SAS ranges from localized obstructive membranes to complex tunnel narrowing and often coexists with other CHD like ventricular septal defect, interrupted aortic arch, and aortic coarctation. Despite generally successful surgeries, SAS recurs in 5%-30% of patients, necessitating reoperation.
View Article and Find Full Text PDFCureus
December 2024
Cardiovascular Surgery, Ayase Heart Hospital, Tokyo, JPN.
Subvalvular aortic stenosis typically manifests at a young age and rarely presents in adulthood. It may cause left ventricular outflow tract stenosis, which requires surgical treatment in severe cases. The coexistence of discrete subvalvular aortic stenosis and quadricuspid aortic valve is a highly unusual finding.
View Article and Find Full Text PDFWorld J Pediatr Congenit Heart Surg
January 2025
Anaesthesiology, Critical Care and Pain Medicine, All India Institute of Medical Sciences - Guwahati, Guwahati, India.
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