Case Report
Copyright ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Nov 6, 2019; 7(21): 3639-3648
Published online Nov 6, 2019. doi: 10.12998/wjcc.v7.i21.3639
Bilateral common carotid artery common trunk with aberrant right subclavian artery combined with right subclavian steal syndrome: A case report
Yuan-Yuan Sun, Guo-Ming Zhang, You-Bin Zhang, Xin Du, Mao-Long Su
Yuan-Yuan Sun, Xin Du, Mao-Long Su, Department of Ultrasound, Xiamen Cardiovascular Hospital Xiamen University, Xiamen 361000, Fujian Province, China
Guo-Ming Zhang, Department of Cardiology, Xiamen Cardiovascular Hospital Xiamen University, Xiamen 361000, Fujian Province, China
You-Bin Zhang, Department of Radiology, Zhongshan Hospital Xiamen University, Xiamen 361000, Fujian Province, China
Author contributions: Sun YY and Zhang GM contributed equally to this work; Sun YY and Du X acquired case information; Su ML designed research; Zhang YB acquired imaging examination data; Sun YY and Zhang GM wrote the paper.
Supported by Fujian Province Medical Innovation Project, No. 2016-CXB-13.
Informed consent statement: Informed written consent was obtained from the patient.
Conflict-of-interest statement: The authors declare that they have no conflicts of interest.
CARE Checklist (2016) statement: The manuscript was prepared and revised according to the CARE Checklist (2016).
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Mao-Long Su, MD, Chief Physician, Department of Ultrasound, Xiamen Cardiovascular Hospital Xiamen University, Hubinnan Road No. 205, Siming District, Xiamen 361000, Fujian Province, China. guomingpaper@126.com
Telephone: +86-592-2992999 Fax: +86-592-2992999
Received: May 6, 2019
Peer-review started: May 8, 2019
First decision: September 9, 2019
Revised: September 23, 2019
Accepted: September 25, 2019
Article in press: September 25, 2019
Published online: November 6, 2019
Processing time: 186 Days and 23.8 Hours
Abstract
BACKGROUND

We report a rare case of numbness in the right hand, finally diagnosed as bilateral common carotid artery common trunk with aberrant right subclavian artery combined with right subclavian steal syndrome and explain the cause of these diseases.

CASE SUMMARY

The patient was a 65-year-old woman. She complained of dizziness, numbness and weakness of the right hand for 6 mo. She was diagnosed with bilateral common carotid artery common trunk with aberrant right subclavian artery combined with right subclavian steal syndrome by ultrasound, enhanced computed tomography, computed tomography angiography and other examinations. Considering the surgical risks, the patient refused the aberrant right subclavian artery stent implantation and was discharged. We hypothesize that these two kinds of deformity and right subclavian steal syndrome may not occur by accident and result from multiple malformations.

CONCLUSION

Bilateral common carotid artery common trunk with aberrant right subclavian artery combined with right subclavian steal syndrome is rare. This case reminds interventional radiologists of the possibility of these abnormalities before surgery.

Keywords: Bilateral common carotid artery common trunk; Aberrant right subclavian artery; Right subclavian steal syndrome; Case report

Core tip: Bilateral common carotid artery common trunk with aberrant right subclavian artery combined with right subclavian steal syndrome is rare. No other similar domestic or foreign cases have been described. We hypothesized that the occurrence of blood steal syndrome may not be accidental and results from multiple malformations. This case reminds surgeons and interventional radiologists to be aware of the possibility of these abnormalities in patients with aortic arch abnormalities before surgery.