Journal of Pediatric Cardiology and Cardiac Surgery

Online ISSN: 2433-1783 Print ISSN: 2433-2720
Japanese Society of Pediatric Cardiology and Cardiac Surgery
Japanese Society of Pediatric Cardiology and Cardiac Surgery Academy Center, 358-5 Yamabuki-cho, Shinju-ku, Tokyo 162-0801, Japan
Journal of Pediatric Cardiology and Cardiac Surgery 4(2): 84-89 (2020)
doi:10.24509/jpccs.20-008

Case ReportCase Report

Idiopathic True Brachial Artery Aneurysm in a 21-Month-Old Infant: A Case Study

1Department of Pediatrics, Osaka University Graduate School of Medicine ◇ Osaka, Japan

2Department of Pediatrics and Neonatology, Osaka General Medical Centre ◇ Osaka, Japan

3Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine ◇ Osaka, Japan

受付日:2020年3月27日Received: March 27, 2020
受理日:2020年5月22日Accepted: May 22, 2020
発行日:2020年7月1日Published: July 1, 2020
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True aneurysms occur only rarely in the peripheral arteries of the upper extremity. As such, a treatment protocol deciding how and when to conduct surgical repair is still unestablished. In this paper, we report the case of a 21-month-old boy who presented with a painless, pulsatile swelling in the mid-arm on the right side; he was subsequently diagnosed with an idiopathic true brachial artery aneurysm. The size of the aneurysm rapidly increased over the course of 2 months and ultrasound examination delineated a thrombus inside the aneurysm. Therefore, the aneurysm was surgically resected and completely repaired by end-to-end anastomosis using cephalic vein grafting. Follow-up angiography showed excellent blood flow within the graft, and there was no stenosis. No neurological complications were observed during the 2 years follow-up period.

Key words: brachial artery aneurysm; idiopathic true aneurysm; infant

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