An atrial septal defect (ASD) is a common congenital heart anomaly that results in irregular blood flow between the systemic and pulmonary circulations due to an opening in the atrial septum. Ostium secondum ASD accounts for a large proportion of these defects and often goes unnoticed during childhood and adolescence. Pulmonary hypertension (PH), affecting a significant number of patients with ostium secondum ASD, is associated with functional limitations, heart failure, and tachyarrhythmias. This case involves a 23-year-old male with a large ostium secondum ASD, moderate PH, and normal left ventricular systolic function, presenting with a rare Crochetage sign on his electrocardiogram (ECG). The patient's clinical presentation, including the presence of the Crochetage sign, was assessed using various diagnostic tools. An ECG identified the characteristic notch in the R wave in the inferior leads, indicative of ASD. Further evaluation, including echocardiography, was performed to assess the size and impact of the ostium secondum ASD. Echocardiography confirmed the presence of a large ASD with moderate PH. The case underscores the importance of recognizing rare signs, like the Crochetage sign, in the diagnosis and management of ASD. It presents a clinical dilemma regarding whether to proceed with the closure of the ostium secondum, given the potential complications associated with complete closure. A multidimensional approach, considering the patient's overall condition and potential risks, is essential for optimal management. This case highlights the need for comprehensive evaluation and timely intervention to improve outcomes in patients with ASD.
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http://dx.doi.org/10.7759/cureus.77373 | DOI Listing |
An atrial septal defect (ASD) is a common congenital heart anomaly that results in irregular blood flow between the systemic and pulmonary circulations due to an opening in the atrial septum. Ostium secondum ASD accounts for a large proportion of these defects and often goes unnoticed during childhood and adolescence. Pulmonary hypertension (PH), affecting a significant number of patients with ostium secondum ASD, is associated with functional limitations, heart failure, and tachyarrhythmias.
View Article and Find Full Text PDFBMJ Case Rep
September 2022
Anesthesiology, Saveetha University Saveetha Medical College and Hospital, Chennai, Tamil Nadu, India.
A woman in her mid-20s who was clinically euthyroid presented with an ostium secondum atrial septal defect for closure. Preoperatively, heart rate ranged from 80 to 110 beats per minute. On the day of surgery, heart rate was 120 beats per minute, which settled after induction.
View Article and Find Full Text PDFInt Heart J
January 2020
Department of Cardiovascular Surgery, The Second Hospital of Jilin University.
Transcatheter closure of ostium secondum atrial septal defect has become an alternative method to surgical closure. However, the incidence of complications and long-term results of using large size (> 40 mm) Amplatzer septal occluders are unknown. This case reported a 59 years old woman, whom received transcatheter closure of atrial septal defect (36 mm) with a 40 mm Amplatzer septal occluder 10 years ago and was diagnosed with heart failure.
View Article and Find Full Text PDFPulmonary agenesis, a rare congenital condition, is incompatible with life when present bilateral, while unilateral agenesis is usually detected in infancy or early childhood. Rare asymptomatic patients may reach adulthood undiagnosed, with signs mimicking common conditions presenting as radiopaque hemithorax with ipsilateral mediastinal shift. Here, we describe a case of a young lady, with history of consanguinity, who presented with complaints, suggestive of lower respiratory tract infection, and was investigated and diagnosed to be a case of right-side pulmonary agenesis with large ostium secondum atrial septal defect.
View Article and Find Full Text PDFBMJ Case Rep
May 2014
Department of Cardiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
A 17-year-old male patient presented with cyanosis, repeated squatting since childhood and haemoptysis since the past 1 month. He had central cyanosis with clubbing. Cardiovasular examination revealed ejection systolic murmur in the pulmonary area with single S2.
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