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A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery
BACKGROUND: Aneurysms of the occipital artery (OA) are rare, with few cases published in the literature. The pathophysiology is unknown, and the presentation is variable. We present a case of a ruptured intracranial aneurysm arising from a branch of the OA. CASE DESCRIPTION: A 36-year-old male with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492441/ https://www.ncbi.nlm.nih.gov/pubmed/34621573 http://dx.doi.org/10.25259/SNI_740_2021 |
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author | Aljuboori, Zaid McGrath, Margaret Jadhav, Rahul Ghodke, Basavaraj Sekhar, Laligam |
author_facet | Aljuboori, Zaid McGrath, Margaret Jadhav, Rahul Ghodke, Basavaraj Sekhar, Laligam |
author_sort | Aljuboori, Zaid |
collection | PubMed |
description | BACKGROUND: Aneurysms of the occipital artery (OA) are rare, with few cases published in the literature. The pathophysiology is unknown, and the presentation is variable. We present a case of a ruptured intracranial aneurysm arising from a branch of the OA. CASE DESCRIPTION: A 36-year-old male with a history of ankylosing spondylitis presented with altered mental status after an assaulted. On examination, he was intubated, with a Glasgow coma scale of 9, and imaging of the head and neck revealed a subdural hematoma of the posterior fossa and the cervical spine. The patient underwent suboccipital craniectomy and C1-5 laminectomy with the evacuation of the subdural hematoma. Postoperative cerebral angiography showed an intracranial aneurysm arising from the retromastoid branch of the OA on the left side. Furthermore, the parent vessel of the aneurysm supplied the left lower half of the cerebellar hemisphere. The aneurysm and the parent vessel were embolized using platinum coils. The patient tolerated the procedure well, and magnetic resonance imaging of the brain showed a minor left-sided cerebellar infarct, which was asymptomatic. The patient was discharged home with a modified Rankin scale of 2. There were no outpatient follow-up data available because the patient lost to follow-up. CONCLUSION: Intracranial OA aneurysms are extremely rare with no clear consensus concerning the management of these aneurysms. They can be treated using endovascular and or open surgical techniques depending on the aneurysm characteristics, patient condition, rupture status, and others. |
format | Online Article Text |
id | pubmed-8492441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-84924412021-10-06 A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery Aljuboori, Zaid McGrath, Margaret Jadhav, Rahul Ghodke, Basavaraj Sekhar, Laligam Surg Neurol Int Case Report BACKGROUND: Aneurysms of the occipital artery (OA) are rare, with few cases published in the literature. The pathophysiology is unknown, and the presentation is variable. We present a case of a ruptured intracranial aneurysm arising from a branch of the OA. CASE DESCRIPTION: A 36-year-old male with a history of ankylosing spondylitis presented with altered mental status after an assaulted. On examination, he was intubated, with a Glasgow coma scale of 9, and imaging of the head and neck revealed a subdural hematoma of the posterior fossa and the cervical spine. The patient underwent suboccipital craniectomy and C1-5 laminectomy with the evacuation of the subdural hematoma. Postoperative cerebral angiography showed an intracranial aneurysm arising from the retromastoid branch of the OA on the left side. Furthermore, the parent vessel of the aneurysm supplied the left lower half of the cerebellar hemisphere. The aneurysm and the parent vessel were embolized using platinum coils. The patient tolerated the procedure well, and magnetic resonance imaging of the brain showed a minor left-sided cerebellar infarct, which was asymptomatic. The patient was discharged home with a modified Rankin scale of 2. There were no outpatient follow-up data available because the patient lost to follow-up. CONCLUSION: Intracranial OA aneurysms are extremely rare with no clear consensus concerning the management of these aneurysms. They can be treated using endovascular and or open surgical techniques depending on the aneurysm characteristics, patient condition, rupture status, and others. Scientific Scholar 2021-09-13 /pmc/articles/PMC8492441/ /pubmed/34621573 http://dx.doi.org/10.25259/SNI_740_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Aljuboori, Zaid McGrath, Margaret Jadhav, Rahul Ghodke, Basavaraj Sekhar, Laligam A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title | A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title_full | A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title_fullStr | A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title_full_unstemmed | A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title_short | A rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
title_sort | rare case of ruptured intracranial aneurysm arising from the retro-mastoid branch of the occipital artery |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492441/ https://www.ncbi.nlm.nih.gov/pubmed/34621573 http://dx.doi.org/10.25259/SNI_740_2021 |
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