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Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report

INTRODUCTION: Carotid artery dissection is a rare but serious condition manifesting with signs and symptoms that closely overlap with other more benign medical diagnoses. This vascular injury, however, can result in debilitating sequelae, including thromboembolic cerebrovascular accidents. CASE REPO...

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Autores principales: McGuire, Duncan, Mielke, Nicholas, Bahl, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436487/
https://www.ncbi.nlm.nih.gov/pubmed/36049190
http://dx.doi.org/10.5811/cpcem.2022.4.56488
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author McGuire, Duncan
Mielke, Nicholas
Bahl, Amit
author_facet McGuire, Duncan
Mielke, Nicholas
Bahl, Amit
author_sort McGuire, Duncan
collection PubMed
description INTRODUCTION: Carotid artery dissection is a rare but serious condition manifesting with signs and symptoms that closely overlap with other more benign medical diagnoses. This vascular injury, however, can result in debilitating sequelae, including thromboembolic cerebrovascular accidents. CASE REPORT: We describe the atypical presentation of a healthy eight-year-old male who presented to the emergency department (ED) with generalized abdominal pain and non-bloody, non-bilious emesis. These symptoms occurred nine days after he sustained blunt head trauma after a non-syncopal fall from standing while playing hockey. He was initially diagnosed with gastroesophageal reflux disease and constipation and was discharged home. The following day he developed an acute headache followed shortly by gait ataxia, prompting a return visit to the ED. Imaging of the head and neck revealed a left internal carotid artery dissection. The patient was started on intravenous unfractionated heparin and admitted to the hospital. He was later discharged symptom-free on therapeutic enoxaparin for eight weeks, followed by daily aspirin therapy. CONCLUSION: Pediatric trauma patients, especially those sustaining insult to the head and cervical spine, are at risk for craniocervical arterial injuries. This rare but dangerous pathology often manifests in a non-specific, delayed fashion making it a challenging diagnosis for physicians to make on the initial medical encounter.1,2 Maintaining a high clinical suspicion for carotid artery dissection is required to make this diagnosis and should guide a thorough history, physical examination, and appropriate imaging in order to improve patient morbidity and mortality. This case emphasizes key clinical features and risk factors of this disease that may help emergency clinicians promptly recognize and treat this entity.
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spelling pubmed-94364872022-09-02 Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report McGuire, Duncan Mielke, Nicholas Bahl, Amit Clin Pract Cases Emerg Med Case Report INTRODUCTION: Carotid artery dissection is a rare but serious condition manifesting with signs and symptoms that closely overlap with other more benign medical diagnoses. This vascular injury, however, can result in debilitating sequelae, including thromboembolic cerebrovascular accidents. CASE REPORT: We describe the atypical presentation of a healthy eight-year-old male who presented to the emergency department (ED) with generalized abdominal pain and non-bloody, non-bilious emesis. These symptoms occurred nine days after he sustained blunt head trauma after a non-syncopal fall from standing while playing hockey. He was initially diagnosed with gastroesophageal reflux disease and constipation and was discharged home. The following day he developed an acute headache followed shortly by gait ataxia, prompting a return visit to the ED. Imaging of the head and neck revealed a left internal carotid artery dissection. The patient was started on intravenous unfractionated heparin and admitted to the hospital. He was later discharged symptom-free on therapeutic enoxaparin for eight weeks, followed by daily aspirin therapy. CONCLUSION: Pediatric trauma patients, especially those sustaining insult to the head and cervical spine, are at risk for craniocervical arterial injuries. This rare but dangerous pathology often manifests in a non-specific, delayed fashion making it a challenging diagnosis for physicians to make on the initial medical encounter.1,2 Maintaining a high clinical suspicion for carotid artery dissection is required to make this diagnosis and should guide a thorough history, physical examination, and appropriate imaging in order to improve patient morbidity and mortality. This case emphasizes key clinical features and risk factors of this disease that may help emergency clinicians promptly recognize and treat this entity. University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2022-08-06 /pmc/articles/PMC9436487/ /pubmed/36049190 http://dx.doi.org/10.5811/cpcem.2022.4.56488 Text en © 2022 McGuire. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) License. See: http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Report
McGuire, Duncan
Mielke, Nicholas
Bahl, Amit
Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title_full Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title_fullStr Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title_full_unstemmed Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title_short Atypical Presentation of Traumatic Pediatric Carotid Artery Dissection: A Case Report
title_sort atypical presentation of traumatic pediatric carotid artery dissection: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436487/
https://www.ncbi.nlm.nih.gov/pubmed/36049190
http://dx.doi.org/10.5811/cpcem.2022.4.56488
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