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Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm
BACKGROUND: Persistent primitive olfactory artery (PPOA) is a rare anomaly of the anterior cerebral artery. We experienced a rare case of subarachnoid hemorrhage caused by a ruptured saccular aneurysm of PPOA. CASE DESCRIPTION: A 72-year-old man was transported to our hospital with sudden headache....
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/PMC8088532/ https://www.ncbi.nlm.nih.gov/pubmed/33948317 http://dx.doi.org/10.25259/SNI_202_2021 |
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author | Yamaki, Tetsu Kondo, Rei Sano, Kenshi Honma, Hiroshi Kuge, Atsushi Saito, Shinjiro Sonoda, Yukihiko |
author_facet | Yamaki, Tetsu Kondo, Rei Sano, Kenshi Honma, Hiroshi Kuge, Atsushi Saito, Shinjiro Sonoda, Yukihiko |
author_sort | Yamaki, Tetsu |
collection | PubMed |
description | BACKGROUND: Persistent primitive olfactory artery (PPOA) is a rare anomaly of the anterior cerebral artery. We experienced a rare case of subarachnoid hemorrhage caused by a ruptured saccular aneurysm of PPOA. CASE DESCRIPTION: A 72-year-old man was transported to our hospital with sudden headache. On examination, World Federation of Neurological Surgeons scale was Grade I, and computed tomography of the head showed subarachnoid hemorrhage in Fisher Group 3. Cerebral angiography showed left PPOA and a 4-mm saccular aneurysm at the hairpin turn. No other abnormalities causing bleeding were observed. Based on these findings, subarachnoid hemorrhage due to a ruptured PPOA aneurysm was diagnosed. As the patient had a ventilatory defect due to emphysema, direct approach to the lesion would have been difficult and an endovascular surgery was performed. Three coils were inserted into the aneurysm, and complete occlusion was achieved. Cerebral vasospasm was not observed, and the patient was discharged 1 month after surgery without any neurologic deficit. CONCLUSION: Most aneurysms of the PPOA are formed at the hairpin turn, as observed in our patient; therefore, a hemodynamic mechanism may be involved in the etiology. To the best of our knowledge, there is no report on treatment using intra-aneurysmal coil embolization, indicating that ours was the first case. As the long-term outcome of intra-aneurysmal coil embolization for PPOA aneurysm is unknown, careful follow-up will be necessary in the future. |
format | Online Article Text |
id | pubmed-8088532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-80885322021-05-03 Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm Yamaki, Tetsu Kondo, Rei Sano, Kenshi Honma, Hiroshi Kuge, Atsushi Saito, Shinjiro Sonoda, Yukihiko Surg Neurol Int Case Report BACKGROUND: Persistent primitive olfactory artery (PPOA) is a rare anomaly of the anterior cerebral artery. We experienced a rare case of subarachnoid hemorrhage caused by a ruptured saccular aneurysm of PPOA. CASE DESCRIPTION: A 72-year-old man was transported to our hospital with sudden headache. On examination, World Federation of Neurological Surgeons scale was Grade I, and computed tomography of the head showed subarachnoid hemorrhage in Fisher Group 3. Cerebral angiography showed left PPOA and a 4-mm saccular aneurysm at the hairpin turn. No other abnormalities causing bleeding were observed. Based on these findings, subarachnoid hemorrhage due to a ruptured PPOA aneurysm was diagnosed. As the patient had a ventilatory defect due to emphysema, direct approach to the lesion would have been difficult and an endovascular surgery was performed. Three coils were inserted into the aneurysm, and complete occlusion was achieved. Cerebral vasospasm was not observed, and the patient was discharged 1 month after surgery without any neurologic deficit. CONCLUSION: Most aneurysms of the PPOA are formed at the hairpin turn, as observed in our patient; therefore, a hemodynamic mechanism may be involved in the etiology. To the best of our knowledge, there is no report on treatment using intra-aneurysmal coil embolization, indicating that ours was the first case. As the long-term outcome of intra-aneurysmal coil embolization for PPOA aneurysm is unknown, careful follow-up will be necessary in the future. Scientific Scholar 2021-04-08 /pmc/articles/PMC8088532/ /pubmed/33948317 http://dx.doi.org/10.25259/SNI_202_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 Yamaki, Tetsu Kondo, Rei Sano, Kenshi Honma, Hiroshi Kuge, Atsushi Saito, Shinjiro Sonoda, Yukihiko Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title | Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title_full | Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title_fullStr | Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title_full_unstemmed | Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title_short | Coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
title_sort | coil embolization of subarachnoid hemorrhage with ruptured persistent primitive olfactory artery aneurysm |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088532/ https://www.ncbi.nlm.nih.gov/pubmed/33948317 http://dx.doi.org/10.25259/SNI_202_2021 |
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