Institutional members access full text with Ovid®

Share this article on:

One Case, 3 Rare Simultaneous Findings: Intramyocardial Bronchogenic Cyst, P.H558R Variant of SCN5A Gene, and Granular Cell Tumor of the Esophagus

Shiferaw, Kebede MD*; Lobrinus, Alexandre J. MD; Grabherr, Silke MD*; Michaud, Katarzyna MD*; Mangin, Patrice MD, PhD*; Schrag, Bettina MD*

The American Journal of Forensic Medicine and Pathology: December 2012 - Volume 33 - Issue 4 - p 335–338
doi: 10.1097/PAF.0b013e318264e9ef
Case Reports

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.

From the *University Centre of Legal Medicine, Lausanne; and †Institute of Clinical Pathology, University Hospital of Geneva, Geneva, Switzerland.

Manuscript received July 14, 2011; accepted June 6, 2012.

The authors report no conflicts of interest.

Reprints: Kebede Shiferaw, MD, Centre Universitaire Romand de Médecine Légale (CURML), Rue du Bugnon 21, 1011 Lausanne, Switzerland. E-mail:

© 2012 Lippincott Williams & Wilkins, Inc.