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Management of Late-Presenting Congenital Combined Heart Defect – Bicuspid Aortic Valve and Ventricular Septal Aneurysm

Patient: Female, 68-year-old Final Diagnosis: Bicuspid aortic valve and ventricular septal aneurysm Symptoms: Cough Medication:— Clinical Procedure: Plastic repair of ascending aorta and interventricular anurysm Specialty: Cardiac surgery OBJECTIVE: Rare disease BACKGROUND: Bicuspid aortic valve is...

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Detalles Bibliográficos
Autores principales: Groudeva, Violeta V., Atzev, Borislav G., Petkov, Dimitar G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081954/
https://www.ncbi.nlm.nih.gov/pubmed/32165609
http://dx.doi.org/10.12659/AJCR.919766
Descripción
Sumario:Patient: Female, 68-year-old Final Diagnosis: Bicuspid aortic valve and ventricular septal aneurysm Symptoms: Cough Medication:— Clinical Procedure: Plastic repair of ascending aorta and interventricular anurysm Specialty: Cardiac surgery OBJECTIVE: Rare disease BACKGROUND: Bicuspid aortic valve is the most common congenital heart malformation, encountered in 1–2% of the population, while interventricular septal defect and patent ductus arteriosus are the most common congenital malformations associated with bicuspid aortic valve. Although bicuspid valve can have no clinical manifestation, patients with bicuspid valve are prone to develop vascular abnormalities. Aortic dilatation is the most common of these abnormalities, which in turn can lead to serious complications and often requires surgical treatment. Coexistence of bicuspid aortic valve and interventricular septal aneurysm is very extremely rare. CASE REPORT: We present a very rare case of a female patient with combined congenital cardiac pathology. The patient was asymptomatic until age 68 years, and presented with nonspecific persistent cough. The diagnostic work-up for the unexplained cough showed normal function of the bicuspid valve and an ascending aorta aneurysm accompanied with interventricular septal aneurysm. The patient was referred for surgery. The diagnostic work-up and the decision for surgical treatment were thoroughly discussed to determine whether it was a true or a false aneurysm. CONCLUSIONS: The presented case is an example of late diagnosis of a congenital cardiac defect. The silent evolution and the scarce clinical presentation led to incidental discovery of the pathology, which was fully assessed only by computed tomography. Although echocardiography is essential for discovering heart defects, non-invasive imaging techniques are required for detailed morphological assessment and for planning optimal surgical treatment.