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Lutembacher’s syndrome accompanied by partial anomalies of pulmonary veins in a 70-year-old male: a case of congenital heart disease in the elderly
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Lutembacher’s syndrome is a rare disease defined as the combination of atrial septal defect and mitral stenosis, which relieves the progression of symptoms resulting from mitral stenosis. We present a case of a previously asymptomatic 70-year-old man having Lutembacher’s syndrome with sinus venosus type of interatrial defect associated with partial anomalous pulmonary venous drainage. Our patient’s only complaint was of mild exertional dyspnea, which started six months prior to referral. Clinical suspicion of the combination of defects arose during transthoracic echocardiography. The patient underwent transesophageal echocardiography and multi-slice computed tomography for defect confirmation. The combination of Lutembacher’s syndrome with this complex deformity of pulmonary venous drainage has rarely been described. Such complex congenital defects with multifaceted physiological repercussions can go largely undiagnosed for the patients affected for most of their lifetimes.
Title: Lutembacher’s syndrome accompanied by partial anomalies of pulmonary veins in a 70-year-old male: a case of congenital heart disease in the elderly
Description:
Lutembacher’s syndrome is a rare disease defined as the combination of atrial septal defect and mitral stenosis, which relieves the progression of symptoms resulting from mitral stenosis.
We present a case of a previously asymptomatic 70-year-old man having Lutembacher’s syndrome with sinus venosus type of interatrial defect associated with partial anomalous pulmonary venous drainage.
Our patient’s only complaint was of mild exertional dyspnea, which started six months prior to referral.
Clinical suspicion of the combination of defects arose during transthoracic echocardiography.
The patient underwent transesophageal echocardiography and multi-slice computed tomography for defect confirmation.
The combination of Lutembacher’s syndrome with this complex deformity of pulmonary venous drainage has rarely been described.
Such complex congenital defects with multifaceted physiological repercussions can go largely undiagnosed for the patients affected for most of their lifetimes.
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