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Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report

BACKGROUND: Spontaneous subarachnoid hemorrhage (SAH) is primarily caused by a ruptured intracranial aneurysm. Perimesencephalic nonaneurysmal SAH (PNSAH) accounts for approximately 5% of all spontaneous SAH. PNSAH displays favorable prognosis. The risk of hemorrhage recurrence is low. We report a c...

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Autores principales: Li, Juan, Fang, Xiang, Yu, Fu-Chao, Du, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107889/
https://www.ncbi.nlm.nih.gov/pubmed/34002145
http://dx.doi.org/10.12998/wjcc.v9.i14.3356
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author Li, Juan
Fang, Xiang
Yu, Fu-Chao
Du, Bin
author_facet Li, Juan
Fang, Xiang
Yu, Fu-Chao
Du, Bin
author_sort Li, Juan
collection PubMed
description BACKGROUND: Spontaneous subarachnoid hemorrhage (SAH) is primarily caused by a ruptured intracranial aneurysm. Perimesencephalic nonaneurysmal SAH (PNSAH) accounts for approximately 5% of all spontaneous SAH. PNSAH displays favorable prognosis. The risk of hemorrhage recurrence is low. We report a case of PNSAH recurrence, occurring within a short time after the initial episode in a patient not receiving antithrombotic or antiplatelet drugs. CASE SUMMARY: A 66-year-old male, without any history of recent trauma or antithrombotic/ antiplatelet medication, suffered two similar episodes of sudden onset of severe headache, nausea, and vomiting. A plain head computed tomography (CT) scan showed subarachnoid blood confined to the anterior part of the brainstem. Platelet count and coagulation function were normal. PNSAH was diagnosed by repeated head CT, magnetic resonance imaging, and cerebral angiography, none of which revealed the source of SAH. The patient was discharged without focal neurological deficits. At 6-mo follow-up, the patient had experienced no sudden onset of severe headache and presented favorable clinical outcome. Studies have reported a few patients with recurrent PNSAH, originating frequently from venous hemorrhage and conventionally associated with venous abnormalities. PNSAH recurs within a short time following the initial onset of symptoms, although the possibility of re-hemorrhage is extremely rare. CONCLUSION: PNSAH recurrence should arouse vigilance; however, the definite source of idiopathic SAH in this case report deserves further attention.
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spelling pubmed-81078892021-05-16 Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report Li, Juan Fang, Xiang Yu, Fu-Chao Du, Bin World J Clin Cases Case Report BACKGROUND: Spontaneous subarachnoid hemorrhage (SAH) is primarily caused by a ruptured intracranial aneurysm. Perimesencephalic nonaneurysmal SAH (PNSAH) accounts for approximately 5% of all spontaneous SAH. PNSAH displays favorable prognosis. The risk of hemorrhage recurrence is low. We report a case of PNSAH recurrence, occurring within a short time after the initial episode in a patient not receiving antithrombotic or antiplatelet drugs. CASE SUMMARY: A 66-year-old male, without any history of recent trauma or antithrombotic/ antiplatelet medication, suffered two similar episodes of sudden onset of severe headache, nausea, and vomiting. A plain head computed tomography (CT) scan showed subarachnoid blood confined to the anterior part of the brainstem. Platelet count and coagulation function were normal. PNSAH was diagnosed by repeated head CT, magnetic resonance imaging, and cerebral angiography, none of which revealed the source of SAH. The patient was discharged without focal neurological deficits. At 6-mo follow-up, the patient had experienced no sudden onset of severe headache and presented favorable clinical outcome. Studies have reported a few patients with recurrent PNSAH, originating frequently from venous hemorrhage and conventionally associated with venous abnormalities. PNSAH recurs within a short time following the initial onset of symptoms, although the possibility of re-hemorrhage is extremely rare. CONCLUSION: PNSAH recurrence should arouse vigilance; however, the definite source of idiopathic SAH in this case report deserves further attention. Baishideng Publishing Group Inc 2021-05-16 2021-05-16 /pmc/articles/PMC8107889/ /pubmed/34002145 http://dx.doi.org/10.12998/wjcc.v9.i14.3356 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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/
spellingShingle Case Report
Li, Juan
Fang, Xiang
Yu, Fu-Chao
Du, Bin
Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title_full Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title_fullStr Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title_full_unstemmed Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title_short Recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: A case report
title_sort recurrent perimesencephalic nonaneurysmal subarachnoid hemorrhage within a short period of time: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107889/
https://www.ncbi.nlm.nih.gov/pubmed/34002145
http://dx.doi.org/10.12998/wjcc.v9.i14.3356
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