Esophageal Duplication Cyst Presenting with Dysphagia in a Middle-Aged Male: A Case Report
Abstract
Esophageal duplication cysts (EDCs) are rare congenital foregut anomalies often presenting with nonspecific gastrointestinal (GI) symptoms in childhood. Diagnosis requires a high index of suspicion and comprehensive work-up. We report a 56-year- old male with type 2 diabetes mellitus and benign prostatic hyperplasia. He presented with a one-month history of intermittent, burning epigastric pain exacerbated by eating and accompanied by nausea. Physical examination revealed mild epigastric tenderness. Upper GI endoscopy showed a bulging lesion in the lower esophagus, a large cardia polyp, a small gastric body polyp, and antral erythema. Endoscopic ultrasound (EUS) identified a well-defined, homogeneous, round lesion (33 × 20 mm) demonstrating acoustic enhancement in the lower esophagus. Contrast-enhanced abdominopelvic computed tomography (CT) revealed an intraluminal, non-enhancing lesion (25 × 26 mm) at the lower esophageal sphincter (LES), suggestive of a duplication cyst. Thoracic imaging showed no abnormalities. Due to persistent symptoms, the patient underwent successful video-assisted thoracoscopic surgery without complications; no recurrences occurred during follow-up. EDCs should be considered in the differential diagnosis of submucosal or intraluminal esophageal lesions, even in adults despite their rarity. EUS yields high accuracy in characterizing these lesions. Thoraco-abdominal CT scans delineate relationships to surrounding structures. For symptomatic lesions, video-assisted thoracoscopic surgery demonstrates a successful outcome with low complication rates.