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Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review
INTRODUCTION AND IMPORTANCE: Carotid stump syndrome (CSS) is a rare cause of recurrent ipsilateral cerebrovascular accidents (CVAs) resulting from completely occluded internal carotid artery (ICA). In this condition, hemodynamic and embolic risks are related to cerebral and retinal ischemic strokes....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130206/ https://www.ncbi.nlm.nih.gov/pubmed/37068458 http://dx.doi.org/10.1016/j.ijscr.2023.108208 |
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author | Alenezi, Saqer Saleem, Athary Alenezi, Ali Alhajri, Omar Khuraibet, Salma Ameer, Ahmed |
author_facet | Alenezi, Saqer Saleem, Athary Alenezi, Ali Alhajri, Omar Khuraibet, Salma Ameer, Ahmed |
author_sort | Alenezi, Saqer |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Carotid stump syndrome (CSS) is a rare cause of recurrent ipsilateral cerebrovascular accidents (CVAs) resulting from completely occluded internal carotid artery (ICA). In this condition, hemodynamic and embolic risks are related to cerebral and retinal ischemic strokes. PRESENTATION OF CASE: A 65-year-old gentleman with multiple comorbidities, presented to our hospital with a sudden painful unilateral vision loss of the right eye. Head CT was done upon arrival, showing no evidence of ischemic or hemorrhagic brain insult and multiple right frontoparietal old infarct lesions were detected. Central retinal artery occlusion diagnosis was confirmed by an ophthalmologist. CT angiogram of the brain and carotids was done and revealed an obliterated, thrombosed, and non-opacified right internal carotid artery from the carotid bifurcation up to intracranial petrous/foramen lacerum. After taking the patient's surgical consent, right carotid stump endarterectomy and ligation of the stump under general anesthesia was done and the postoperative period was uneventful. CLINICAL DISCUSSION: CSS is an uncommon underlying etiology, causing recurrent stroke events. The clinical features of this syndrome include cerebral and ophthalmology symptoms. Diagnosis of CSS relies on imaging modalities. Internal carotid artery stump surgical excision through the ipsilateral ECA endarterectomy is the gold standard for CSS treatment. CONCLUSION: Despite being a rare entity, CSS is a treatable cause of retinal embolic events TIAs. Therefore, it is important to raise awareness of such condition. The presented case demonstrates the diagnosis, management and prognosis of CSS. |
format | Online Article Text |
id | pubmed-10130206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101302062023-04-27 Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review Alenezi, Saqer Saleem, Athary Alenezi, Ali Alhajri, Omar Khuraibet, Salma Ameer, Ahmed Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Carotid stump syndrome (CSS) is a rare cause of recurrent ipsilateral cerebrovascular accidents (CVAs) resulting from completely occluded internal carotid artery (ICA). In this condition, hemodynamic and embolic risks are related to cerebral and retinal ischemic strokes. PRESENTATION OF CASE: A 65-year-old gentleman with multiple comorbidities, presented to our hospital with a sudden painful unilateral vision loss of the right eye. Head CT was done upon arrival, showing no evidence of ischemic or hemorrhagic brain insult and multiple right frontoparietal old infarct lesions were detected. Central retinal artery occlusion diagnosis was confirmed by an ophthalmologist. CT angiogram of the brain and carotids was done and revealed an obliterated, thrombosed, and non-opacified right internal carotid artery from the carotid bifurcation up to intracranial petrous/foramen lacerum. After taking the patient's surgical consent, right carotid stump endarterectomy and ligation of the stump under general anesthesia was done and the postoperative period was uneventful. CLINICAL DISCUSSION: CSS is an uncommon underlying etiology, causing recurrent stroke events. The clinical features of this syndrome include cerebral and ophthalmology symptoms. Diagnosis of CSS relies on imaging modalities. Internal carotid artery stump surgical excision through the ipsilateral ECA endarterectomy is the gold standard for CSS treatment. CONCLUSION: Despite being a rare entity, CSS is a treatable cause of retinal embolic events TIAs. Therefore, it is important to raise awareness of such condition. The presented case demonstrates the diagnosis, management and prognosis of CSS. Elsevier 2023-04-15 /pmc/articles/PMC10130206/ /pubmed/37068458 http://dx.doi.org/10.1016/j.ijscr.2023.108208 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Alenezi, Saqer Saleem, Athary Alenezi, Ali Alhajri, Omar Khuraibet, Salma Ameer, Ahmed Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title | Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title_full | Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title_fullStr | Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title_full_unstemmed | Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title_short | Sudden unilateral eye pain with vision loss related to carotid stump syndrome; A case report and literature review |
title_sort | sudden unilateral eye pain with vision loss related to carotid stump syndrome; a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130206/ https://www.ncbi.nlm.nih.gov/pubmed/37068458 http://dx.doi.org/10.1016/j.ijscr.2023.108208 |
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