Tracheal Compression by Aberrant Innominate Artery: A Case Report

The brachiocephalic trunk arises from the convexity of the aortic arch, posterior to the manubrium sterni. In rare cases, the origin of the brachiocephalic trunk is shifted to the left of the midline, crosses the trachea through an oblique course, and rises upwards. Sometimes this aberrant artery du...

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Main Authors: Ankit Agarwal, Nidhi Bedi, Pankaj Abrol, Ankit Parakh, Renu Sharma
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2025-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/20754/72935_CE[Ra1]_F(SL)_PF1(KrA_SL)_redo_PFA(IS)_PB(KrA_IS)_PN(IS).pdf
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author Ankit Agarwal
Nidhi Bedi
Pankaj Abrol
Ankit Parakh
Renu Sharma
author_facet Ankit Agarwal
Nidhi Bedi
Pankaj Abrol
Ankit Parakh
Renu Sharma
author_sort Ankit Agarwal
collection DOAJ
description The brachiocephalic trunk arises from the convexity of the aortic arch, posterior to the manubrium sterni. In rare cases, the origin of the brachiocephalic trunk is shifted to the left of the midline, crosses the trachea through an oblique course, and rises upwards. Sometimes this aberrant artery due to an anomalous course can cause a triad of symptoms consisting of cough, stridor, and occasional apnoea known as innominate artery compression syndrome. Here one such case is presented in which, a nine-month-old infant presented with complaints of recurrent cough and noisy breathing since 10 days of age. The infant had a history of frequent hospital admissions for cough since one month of age where he was given nebulisation but with only partial response. A bronchoscopy was done which was suggestive of mid-tracheal compression. Contrast-Enhanced Computed Tomography (CECT) chest confirmed the diagnosis and the child was then referred to a cardiac surgeon for further management. It is important to note that compression of the trachea or tracheobronchial tree by congenital vascular anomalies is not an uncommon cause of stridor and should always be considered a differential diagnosis while evaluating such cases.
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spelling doaj-art-d55ec83a5d12498ca9f81e28e397bc732025-08-20T02:28:02ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2025-03-01193030410.7860/JCDR/2025/72935.20754Tracheal Compression by Aberrant Innominate Artery: A Case ReportAnkit Agarwal0Nidhi Bedi1Pankaj Abrol2Ankit Parakh3Renu Sharma4Junior Resident, Department of Paediatrics, The Faculty of Medicine and Health Sciences, Gurugram, Haryana, India.Professor, Department of Paediatrics, The Faculty of Medicine and Health Sciences, Gurugram, Haryana, India.Professor and Head, Department of Paediatrics, The Faculty of Medicine and Health Sciences, Gurugram, Haryana, India.Consultant Paediatric Pulmonologist, Department of Paediatrics, BLK MAX Hospital, Gurugram, Haryana, India.Senior Resident, Department of Paediatrics, The Faculty of Medicine and Health Sciences, Gurugram, Haryana, India.The brachiocephalic trunk arises from the convexity of the aortic arch, posterior to the manubrium sterni. In rare cases, the origin of the brachiocephalic trunk is shifted to the left of the midline, crosses the trachea through an oblique course, and rises upwards. Sometimes this aberrant artery due to an anomalous course can cause a triad of symptoms consisting of cough, stridor, and occasional apnoea known as innominate artery compression syndrome. Here one such case is presented in which, a nine-month-old infant presented with complaints of recurrent cough and noisy breathing since 10 days of age. The infant had a history of frequent hospital admissions for cough since one month of age where he was given nebulisation but with only partial response. A bronchoscopy was done which was suggestive of mid-tracheal compression. Contrast-Enhanced Computed Tomography (CECT) chest confirmed the diagnosis and the child was then referred to a cardiac surgeon for further management. It is important to note that compression of the trachea or tracheobronchial tree by congenital vascular anomalies is not an uncommon cause of stridor and should always be considered a differential diagnosis while evaluating such cases.https://jcdr.net/articles/PDF/20754/72935_CE[Ra1]_F(SL)_PF1(KrA_SL)_redo_PFA(IS)_PB(KrA_IS)_PN(IS).pdfaortic arch syndromesbrachiocephalic trunktracheal stenosis
spellingShingle Ankit Agarwal
Nidhi Bedi
Pankaj Abrol
Ankit Parakh
Renu Sharma
Tracheal Compression by Aberrant Innominate Artery: A Case Report
Journal of Clinical and Diagnostic Research
aortic arch syndromes
brachiocephalic trunk
tracheal stenosis
title Tracheal Compression by Aberrant Innominate Artery: A Case Report
title_full Tracheal Compression by Aberrant Innominate Artery: A Case Report
title_fullStr Tracheal Compression by Aberrant Innominate Artery: A Case Report
title_full_unstemmed Tracheal Compression by Aberrant Innominate Artery: A Case Report
title_short Tracheal Compression by Aberrant Innominate Artery: A Case Report
title_sort tracheal compression by aberrant innominate artery a case report
topic aortic arch syndromes
brachiocephalic trunk
tracheal stenosis
url https://jcdr.net/articles/PDF/20754/72935_CE[Ra1]_F(SL)_PF1(KrA_SL)_redo_PFA(IS)_PB(KrA_IS)_PN(IS).pdf
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