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Introduction: The Gerbode defect is a rare cardiac anomaly characterised by abnormal communication between the left ventricle and right atrium. Although primarily congenital, it can also be acquired, typically as a complication of myocardial infarction or infective endocarditis. This report examines a unique case of multivalvular infective endocarditis caused by group B Streptococcal bacteraemia, which led to the development of an acquired Gerbode defect.
Case Description: A 64-year-old male patient presented with symptoms of fever and dyspnoea and was diagnosed with group B Streptococcal bacteraemia. Transoesophageal echocardiography (TOE) and cardiac magnetic resonance were used to assess the extent of valvular involvement and detect any underlying structural abnormalities. Comprehensive clinical, microbiological and imaging evaluations were performed to confirm the diagnosis.
Discussion: A transthoracic echocardiography revealed multivalvular vegetations and a newly detected left ventricle-to-right atrium shunt, consistent with a Gerbode defect. Cardiovascular magnetic resonance imaging confirmed the acquired defect. Surgery was considered but deemed too high a risk due to the likelihood of postoperative dialysis and a greater than 50% morality risk. After discussing these risks, the patient and family opted for conservative management, and palliative care was initiated.
Conclusion: This case highlights the rare development of an acquired Gerbode defect in the context of multivalvular infective endocarditis due to group B Streptococcus. Early diagnosis using advanced imaging techniques is critical for proper management. Surgical intervention remains a key therapeutic option, and a multidisciplinary approach is essential for optimising patient outcomes in such complex cases.
Learning Points: An acquired Gerbode defect (left ventricular to right atrial shunt) is a rare but critical complication of infective endocarditis.Infective endocarditis caused by group B in adults, though uncommon, carries a high risk of complications and mortality, especially in prosthetic valve patients.Early transoesophageal echocardiography is essential for identifying structural complications of infective endocarditis.
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http://dx.doi.org/10.12890/2025_005357 | DOI Listing |
Pediatr Cardiol
September 2025
Hacettepe University, Pediatric Cardiovascular Surgery, Ankara, Türkiye.
We report an unusual case of a 13-year-old boy who sustained multiple traumatic cardiac injuries-including ventricular septal and Gerbode defects, aortic dissection, and severe tricuspid regurgitation (TR)-following a high-pressure truck tire explosion. The patient underwent successful endovascular and surgical repair, with full recovery observed at the 1-year follow-up. This case highlights the importance of thorough evaluation and individualized management in pediatric patients with complex cardiac trauma resulting from uncommon high-energy mechanisms.
View Article and Find Full Text PDFThis case report describes a 62-year-old female with a history of heart failure with preserved ejection fraction (HFpEF) who presented to the emergency department with heart failure exacerbation. She was initially diagnosed with bilateral pleural effusions and treated with thoracentesis and diuretics. When follow-up indicated a lack of improvement, an ischemic workup was ordered.
View Article and Find Full Text PDFJACC Case Rep
August 2025
Division of Cardiology, MedStar Heart and Vascular Institute, MedStar Washington Hospital Center, Washington, DC, USA. Electronic address:
Background: Iatrogenic ventricular septal defects (VSDs) are rare but important complications of transcatheter aortic valve replacement (TAVR). In patients who develop conduction abnormalities post-TAVR, the presence of a VSD can complicate pacing strategies.
Case Summary: We report 2 cases of perimembranous VSDs after TAVR, both complicated by conduction disease and managed with left bundle branch pacing (LBBP).
JACC Case Rep
August 2025
Keck School of Medicine of USC, Rolling Hills Estates, California, USA; Division of Pediatric Cardiology, Los Angeles General Medical Center, Los Angeles, California, USA.
Background: A Gerbode defect is a rare communication between the left ventricle and right atrium. Patients with congenital Gerbode defects require prompt diagnosis and medical therapy to temporize their disease until more definitive surgical correction can occur.
Case Summary: A 3-day-old male infant presented to urgent care after his mother noticed episodic cyanosis of the lips and tachypnea that self-resolved.
Reports (MDPI)
July 2025
Second Internal Medical Department, George Emil Palade University of Medicine, Pharmacy, Science and Technology, 540142 Târgu Mureș, Romania.
Infective endocarditis (IE) is a serious condition with rising incidence, frequently caused by . However, cases involving rare congenital anomalies such as Gerbode's defect are uncommon. This report presents the first documented case of IE in a patient with a congenital Gerbode defect complicated by DRESS syndrome-a severe, drug-induced hypersensitivity reaction typically triggered by antibiotics like oxacillin.
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