Symptomatic Very Delayed Parent Artery Occlusion After Flow Diversion Stent Embolization
Flow diversion stents (FDSs) are constructed from high-density braided mesh, which alters intra-aneurysmal hemodynamics and leads to aneurysm occlusion by inducing thrombus formation. Although there are potential complications associated with FDS embolization, one of the serious complications is the...
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| Published in | Neurologia medico-chirurgica Vol. 56; no. 6; pp. 350 - 353 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Japan
The Japan Neurosurgical Society
01.01.2016
THE JAPAN NEUROSURGICAL SOCIETY |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0470-8105 1349-8029 1349-8029 |
| DOI | 10.2176/nmc.cr.2016-0053 |
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| Summary: | Flow diversion stents (FDSs) are constructed from high-density braided mesh, which alters intra-aneurysmal hemodynamics and leads to aneurysm occlusion by inducing thrombus formation. Although there are potential complications associated with FDS embolization, one of the serious complications is the parent artery occlusion due to the in-stent thrombosis. A 72-year-old woman with a symptomatic giant fusiform aneurysm in the cavernous segment of ICA underwent single-layer pipeline embolization device (PED) embolization. Six-month and 1-year follow-up conventional angiographies showed the residual blood flow in the aneurysm. Two-year follow-up MRI showed the aneurysm sac shrinkage and the antiplatelet therapy was discontinued. The patient suffered from symptomatic parent artery occlusion due to the in-stent thrombosis, 4 months after antiplatelet therapy discontinuation. The patient with the incompletely occluded aneurysm after PED embolization should be given long-term antiplatelet therapy because of the risk of delayed parent artery occlusion. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conflicts of Interest Disclosure All authors have registered online self-reported conflict of interest disclosure statement forms through the website for the Japan neurological society. No benefits in any form have been or will be received from any commercial party directly to the subject of this study. Informed consent of the patient for the use of this information was obtained. Institutional review board approval is not required for this type of retrospective study at our institution. |
| ISSN: | 0470-8105 1349-8029 1349-8029 |
| DOI: | 10.2176/nmc.cr.2016-0053 |