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Unrepaired Tetralogy of Fallot in Adulthood

Authors:
John Dickey, M.D.; Christopher Phelan, M.D.

Abstract

This case report describes a 29-year-old man with longstanding exertional dyspnea, visual blurring, and headaches who was diagnosed with tetralogy of Fallot after immigrating to the United States. Imaging revealed classic features: overriding aorta, large ventricular septal defect, right ventricular hypertrophy, and subpulmonic stenosis. Clinical signs included a harsh holosystolic murmur and high hemoglobin levels; symptoms improved with squatting due to reversal of right-to-left shunting. Surgical repair involved pulmonary valvotomy, VSD closure, resection of obstructive muscle bundles, and infundibular patching. Postoperatively, the patient showed marked symptomatic improvement.

Keywords: tetralogy of Fallot congenital heart disease ventricular septal defect overriding aorta right ventricular hypertrophy cyanotic heart defect squatting response echocardiography pulmonary stenosis surgical repair
DOI: https://doi.ms/10.00420/ms/8017/SGRIV/VZU | Volume: 382 | Issue: 25 | Views: 0
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