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Partial atrioventricular septal defect (AVSD) is a congenital heart anomaly that typically manifests in childhood and rarely presents in elderly patients. However, this anomaly can lead to hemodynamically significant cardiopulmonary complications when left untreated. In this report, we present a case of a 68-year-old male patient who presented with symptoms of heart failure and atrial flutter and was found to have partial AVSD incidentally discovered by echocardiography. He was stabilized with diuretics and beta-blockers, and anticoagulation therapy was initiated, given his risk for thromboembolism as per his CHA2DS2VASc2 score. He was subsequently referred for surgical repair, which he declined, opting for medical therapy. The patient was regularly followed up as an outpatient with improvement of symptoms on medical therapy. This case highlights the severe complications of unrepaired partial AVSD in adulthood, highlighting the need for early diagnosis and intervention, since late identification in adulthood can result in significant morbidity. However, in cases where surgery is not possible or declined, patients can be adequately optimized medically to improve overall quality of life and decrease morbidity and mortality associated with this untreated anomaly.
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http://dx.doi.org/10.7759/cureus.89224 | DOI Listing |
Open Access Rheumatol
August 2025
Department of Rheumatology and Immunology, the First Affiliated Hospital, Jinan University, Guangzhou, 510632, People's Republic of China.
Objective: To evaluate the efficacy of baricitinib in combination therapy for managing refractory, rapidly progressive systemic sclerosis (SSc) with severe cardiac conduction defects and interstitial lung disease (ILD).
Methods: A 48-year-old male patient with SSc complicated by significant cardiac enlargement, third-degree atrioventricular block, heart failure, progressive ILD, and partial intestinal obstruction was included in the study. Prior treatments with mycophenolate mofetil (MMF), tacrolimus, and cyclophosphamide (CTX) had shown limited efficacy.
Cureus
August 2025
Pediatric Cardiology, Kings County Hospital Center, Brooklyn, USA.
Partial atrioventricular septal defect (AVSD) is a congenital heart anomaly that typically manifests in childhood and rarely presents in elderly patients. However, this anomaly can lead to hemodynamically significant cardiopulmonary complications when left untreated. In this report, we present a case of a 68-year-old male patient who presented with symptoms of heart failure and atrial flutter and was found to have partial AVSD incidentally discovered by echocardiography.
View Article and Find Full Text PDFAnn Pediatr Cardiol
July 2025
Department of Cardiothoracic and Vascular Surgery, All India Institute of Medical Sciences, New Delhi, India.
Atrioventricular septal defect (AVSD) with cor triatriatum sinister (CTS) is a rare congenital anomalous combination. Few cases of AVSD and CTS have been reported in the literature. However, an isolated case of CTS with partial AVSD, left superior vena cava, and unroofed coronary sinus in an adult has not been reported in the literature.
View Article and Find Full Text PDFMultimed Man Cardiothorac Surg
August 2025
B6-106 University Hospital, LHSC, London, Ontario, Canada
Re-operation following previous congenital heart repair can be challenging. We present a 38-year-old female with a history of partial atrioventricular septal defect repair in infancy who developed severe mitral regurgitation due to a cleft anterior mitral leaflet. Given her anatomy and prior sternotomy, we performed a redo minimally invasive endoscopic mitral valve repair via right anterolateral minithoracotomy access.
View Article and Find Full Text PDFReports (MDPI)
May 2025
Department of Cardiology, Division of Arrhythmology, "Santa Maria della Pietà" Hospital, 80035 Nola, Italy.
Background and Clinical Significance: Scimitar Syndrome is a rare congenital cardiopulmonary anomaly characterized by partial anomalous pulmonary venous return, often requiring early surgical correction. It may coexist with other congenital or acquired cardiovascular anomalies, including valvular diseases such as mitral regurgitation. When surgical correction of Scimitar Syndrome is combined with mitral valve annuloplasty, the proximity to the atrioventricular node may potentially predispose patients to late-onset conduction disturbances, although causality remains speculative.
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