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Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type
There is consensus that intracranial dural arteriovenous fistulae (dAVF) with direct (non-sinus-type) or indirect (sinus-type) retrograde filling of a leptomeningeal vein should be treated due to the high risk of neurological deficits and hemorrhage. No consensus exists on treatment modality (surger...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117260/ https://www.ncbi.nlm.nih.gov/pubmed/21614428 http://dx.doi.org/10.1007/s10143-011-0318-5 |
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author | Wachter, Dorothee Hans, Franz Psychogios, Marios-Nikos Knauth, Michael Rohde, Veit |
author_facet | Wachter, Dorothee Hans, Franz Psychogios, Marios-Nikos Knauth, Michael Rohde, Veit |
author_sort | Wachter, Dorothee |
collection | PubMed |
description | There is consensus that intracranial dural arteriovenous fistulae (dAVF) with direct (non-sinus-type) or indirect (sinus-type) retrograde filling of a leptomeningeal vein should be treated due to the high risk of neurological deficits and hemorrhage. No consensus exists on treatment modality (surgery and/or embolization) and, if surgery is performed, on the best surgical strategy. This series aims to evaluate the role of surgery in the management of aggressive dAVFs. Forty-two patients underwent surgery. Opening and packing the sinus with thrombogenic material was performed in 9 of the 12 sinus-type dAVFs. In two sinus-type fistulae of the cavernous sinus and 1 of the torcular, microsurgery was used as prerequisite for subsequent embolization by providing access to the sinus. In the 30 non-sinus-type dAVFs, surgery consisted of interruption of the draining vein at the intradural entry point. In 41 patients undergoing 43 operations, elimination of the dAVF was achieved (97.6%). In one case, a minimal venous drainage persisted after surgery. The transient surgical morbidity was 11.9% (n = 5) and the permanent surgical morbidity 7.1% (n = 3). Our surgical strategy was to focus on the arterialized leptomeningeal vein in the non-sinus-type and on the arterialized sinus segment in the sinus-type dAVFs allowing us to obliterate all but one dAVF with a low morbidity rate. We therefore propose that microsurgery should be considered early in the treatment of both types of aggressive dAVFs. In selected cases of cavernous sinus dAVFs, the role of microsurgery is reduced to that of an adjunct to endovascular therapy. |
format | Online Article Text |
id | pubmed-3117260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-31172602011-07-14 Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type Wachter, Dorothee Hans, Franz Psychogios, Marios-Nikos Knauth, Michael Rohde, Veit Neurosurg Rev Original Article There is consensus that intracranial dural arteriovenous fistulae (dAVF) with direct (non-sinus-type) or indirect (sinus-type) retrograde filling of a leptomeningeal vein should be treated due to the high risk of neurological deficits and hemorrhage. No consensus exists on treatment modality (surgery and/or embolization) and, if surgery is performed, on the best surgical strategy. This series aims to evaluate the role of surgery in the management of aggressive dAVFs. Forty-two patients underwent surgery. Opening and packing the sinus with thrombogenic material was performed in 9 of the 12 sinus-type dAVFs. In two sinus-type fistulae of the cavernous sinus and 1 of the torcular, microsurgery was used as prerequisite for subsequent embolization by providing access to the sinus. In the 30 non-sinus-type dAVFs, surgery consisted of interruption of the draining vein at the intradural entry point. In 41 patients undergoing 43 operations, elimination of the dAVF was achieved (97.6%). In one case, a minimal venous drainage persisted after surgery. The transient surgical morbidity was 11.9% (n = 5) and the permanent surgical morbidity 7.1% (n = 3). Our surgical strategy was to focus on the arterialized leptomeningeal vein in the non-sinus-type and on the arterialized sinus segment in the sinus-type dAVFs allowing us to obliterate all but one dAVF with a low morbidity rate. We therefore propose that microsurgery should be considered early in the treatment of both types of aggressive dAVFs. In selected cases of cavernous sinus dAVFs, the role of microsurgery is reduced to that of an adjunct to endovascular therapy. Springer-Verlag 2011-05-26 2011 /pmc/articles/PMC3117260/ /pubmed/21614428 http://dx.doi.org/10.1007/s10143-011-0318-5 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Wachter, Dorothee Hans, Franz Psychogios, Marios-Nikos Knauth, Michael Rohde, Veit Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title | Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title_full | Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title_fullStr | Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title_full_unstemmed | Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title_short | Microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
title_sort | microsurgery can cure most intracranial dural arteriovenous fistulae of the sinus and non-sinus type |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117260/ https://www.ncbi.nlm.nih.gov/pubmed/21614428 http://dx.doi.org/10.1007/s10143-011-0318-5 |
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