A case of Kommerell diverticulum in adolescence presented with dysphagia
Hiroharu Shinjo, Hirono Satokawa, Hiroki Wakamatsu, Hitoshi Yokoyama

TL;DR
A 13-year-old boy with a rare aortic anomaly called Kommerell diverticulum successfully underwent surgery to relieve swallowing issues and weight loss.
Contribution
This case report presents a rare adolescent case of Kommerell diverticulum successfully treated with graft replacement surgery.
Findings
Surgical graft replacement successfully treated Kommerell diverticulum in a 13-year-old with dysphagia and weight loss.
Postoperative imaging confirmed no residual esophageal stenosis following the procedure.
The approach allowed effective treatment during adolescence without complications.
Abstract
Kommerell diverticulum (KD) with right aortic arch and aberrant left subclavian artery (ALSCA) is a rare congenital aortic anomaly. To improve organ compression symptoms and avoid rupture of aneurysms in adulthood (19 years old–), surgical treatment is considered the only curative option. However, in childhood (–18 years old), several problems regarding approach and technique selection have been reported. Surgical treatment for KD in infancy (birth–2 years old) has been reported recently, but rarely in adolescence (13–19 years old). We herein report a case of KD in which the patient underwent graft replacement during adolescence. A 13-year-old boy was admitted to our hospital presenting with dysphagia and body weight loss. Esophagography showed upper esophageal stenosis caused by extrinsic compression. Contrast-enhanced computer tomography showed saccular aneurysm formation of KD with…
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Taxonomy
TopicsAortic Disease and Treatment Approaches · Cardiac Structural Anomalies and Repair · Congenital Heart Disease Studies
