Evidence map›Paper›PMID 38678483›Full record

ArticleSurgical case reports2024

A case of Kommerell diverticulum in adolescence presented with dysphagia.

Hiroharu Shinjo, Hirono Satokawa, Hiroki Wakamatsu, Hitoshi Yokoyama

Abstract read
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Article in Surgical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hiroharu ShinjoDepartment of Cardiovascular Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan. hshinjo-hgh@hoshipital.jp.ORCID http://orcid.org/0000-0002-0506-4199
Hirono SatokawaDepartment of Cardiovascular Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hiroki WakamatsuDepartment of Cardiovascular Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hitoshi YokoyamaDepartment of Cardiovascular Surgery, Fukushima Medical University School of Medicine, Fukushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKommerell 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. CASE PRESENTATION: 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 right aortic arch (RAA) and ALSCA. Elective surgery including KD resection and graft replacement of the descending aorta was performed via right thoracotomy under partial extracorporeal circulation. The ALSCA was reconstructed by graft interposition. No postoperative complication was observed. Follow-up esophagography showed no residual stenosis.

conclusionWe experienced a case of KD with dysphagia and weight loss in adolescence, which was successfully treated with surgery. Graft replacement could be an effective treatment option, facilitating recovery even during the growth period.

Indexed as

AdolescenceDysphagiaKommerell diverticulum

Identifiers

PMID38678483
PMCPMC11056346

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