1. One case, 3 rare simultaneous findings: intramyocardial bronchogenic cyst, P.H558R variant of SCN5A gene, and granular cell tumor of the esophagus.
- Author
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Shiferaw K, Lobrinus AJ, Grabherr S, Michaud K, Mangin P, and Schrag B
- Subjects
- Adult, Arrhythmias, Cardiac etiology, Fibrosis, Forensic Pathology, Heart Arrest etiology, Heart Ventricles pathology, Heterozygote, Humans, Male, Myocardium pathology, Pericardium pathology, Bronchogenic Cyst pathology, Death, Sudden etiology, Esophageal Neoplasms pathology, Granular Cell Tumor pathology, Mutation, NAV1.5 Voltage-Gated Sodium Channel genetics
- Abstract
We describe the sudden death of a 42-year-old white man. The decedent was a healthy young man with a short clinical history of chest pain, fatigue, dizziness, and pyrosis. Two weeks before his death, he underwent medical evaluation for the aforementioned symptoms. Electrocardiogram, chest x-ray, and serum troponin were all within normal limits. Gastroesophageal reflux disease was suspected, and the decedent was treated with omeprazole. Medicolegal autopsy disclosed an incidental intramyocardial bronchogenic cyst and p.H558R variant of the SCN5A gene. The cyst was located between the epicardium and myocardium of the posterior face of the left superior ventricular wall, adjacent to the base of the heart. An incidental granular cell tumor of the esophagus was also identified, which was likely unrelated to death.
- Published
- 2012
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