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Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk
INTRODUCTION: Developmental venous anomalies (DVAs) have traditionally been defined as non-pathological congenital lesions. Compared to isolated DVAs, the association of DVAs with arteriovenous shunts seems to have a more adverse clinical connotation. In this review, we describe the association betw...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071040/ https://www.ncbi.nlm.nih.gov/pubmed/37025268 http://dx.doi.org/10.3389/fsurg.2023.1141857 |
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author | Agosti, Edoardo De Maria, Lucio Panciani, Pier Paolo Serioli, Simona Mardighian, Dikran Fontanella, Marco Maria Lanzino, Giuseppe |
author_facet | Agosti, Edoardo De Maria, Lucio Panciani, Pier Paolo Serioli, Simona Mardighian, Dikran Fontanella, Marco Maria Lanzino, Giuseppe |
author_sort | Agosti, Edoardo |
collection | PubMed |
description | INTRODUCTION: Developmental venous anomalies (DVAs) have traditionally been defined as non-pathological congenital lesions. Compared to isolated DVAs, the association of DVAs with arteriovenous shunts seems to have a more adverse clinical connotation. In this review, we describe the association between DVA and dAVF and discuss the hemorrhagic risk. We also advance a hypothesis about the potential de novo formation of a DVA and challenge the dogma about their “developmental” or “congenital” nature. METHODS: A systematic review of the literature on the association of DVA and dAVF was performed in accordance with the PRISMA-P (Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols) guidelines. RESULTS: A number of 678 papers was initially identified, but only 9 studies were included in the final qualitative analysis. Most of the patients presented with bleeding (56%), with a median GCS of 14 (range 10–15). In 56% of the cases the DVA had a supratentorial location. Supratentorial DVAs mostly drained in the superior sagittal sinus (80%), while all of infratentorial/combined DVAs drained in deep ependymal veins of the 4th ventricle. All the supratentorial dAVFs drained into the superior sagittal sinus, while the infratentorial/combined dAVFs mostly drained in the jugular bulb, Vein of Rosenthal, or transverse-sigmoid sinuses (75%). Most of the dAVFs were classified as Cognard type IIa + b (67%), while in a smaller number of cases type I (22%) and type V (11%). The dAVF was the target of treatment in each case and most patients underwent endovascular treatment (78%). The dAVF was completely occluded in 78% of cases and no periprocedural complications were reported. CONCLUSION: The clinical presentation, radiological findings, and treatment outcomes of DVAs and associated dAVFs have been discussed. Despite the general opinion that DVAs are benign congenital lesions, increasing epidemiological and radiological evidence supports a potential acquired origin, and the venous system seem to play a pivotal role in their post-natal genesis and development. |
format | Online Article Text |
id | pubmed-10071040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100710402023-04-05 Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk Agosti, Edoardo De Maria, Lucio Panciani, Pier Paolo Serioli, Simona Mardighian, Dikran Fontanella, Marco Maria Lanzino, Giuseppe Front Surg Surgery INTRODUCTION: Developmental venous anomalies (DVAs) have traditionally been defined as non-pathological congenital lesions. Compared to isolated DVAs, the association of DVAs with arteriovenous shunts seems to have a more adverse clinical connotation. In this review, we describe the association between DVA and dAVF and discuss the hemorrhagic risk. We also advance a hypothesis about the potential de novo formation of a DVA and challenge the dogma about their “developmental” or “congenital” nature. METHODS: A systematic review of the literature on the association of DVA and dAVF was performed in accordance with the PRISMA-P (Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols) guidelines. RESULTS: A number of 678 papers was initially identified, but only 9 studies were included in the final qualitative analysis. Most of the patients presented with bleeding (56%), with a median GCS of 14 (range 10–15). In 56% of the cases the DVA had a supratentorial location. Supratentorial DVAs mostly drained in the superior sagittal sinus (80%), while all of infratentorial/combined DVAs drained in deep ependymal veins of the 4th ventricle. All the supratentorial dAVFs drained into the superior sagittal sinus, while the infratentorial/combined dAVFs mostly drained in the jugular bulb, Vein of Rosenthal, or transverse-sigmoid sinuses (75%). Most of the dAVFs were classified as Cognard type IIa + b (67%), while in a smaller number of cases type I (22%) and type V (11%). The dAVF was the target of treatment in each case and most patients underwent endovascular treatment (78%). The dAVF was completely occluded in 78% of cases and no periprocedural complications were reported. CONCLUSION: The clinical presentation, radiological findings, and treatment outcomes of DVAs and associated dAVFs have been discussed. Despite the general opinion that DVAs are benign congenital lesions, increasing epidemiological and radiological evidence supports a potential acquired origin, and the venous system seem to play a pivotal role in their post-natal genesis and development. Frontiers Media S.A. 2023-03-21 /pmc/articles/PMC10071040/ /pubmed/37025268 http://dx.doi.org/10.3389/fsurg.2023.1141857 Text en © 2023 Agosti, De Maria, Panciani, Serioli, Mardighian, Fontanella and Lanzino. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Agosti, Edoardo De Maria, Lucio Panciani, Pier Paolo Serioli, Simona Mardighian, Dikran Fontanella, Marco Maria Lanzino, Giuseppe Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title | Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title_full | Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title_fullStr | Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title_full_unstemmed | Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title_short | Developmental venous anomaly associated with dural arteriovenous fistula: Etiopathogenesis and hemorrhagic risk |
title_sort | developmental venous anomaly associated with dural arteriovenous fistula: etiopathogenesis and hemorrhagic risk |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071040/ https://www.ncbi.nlm.nih.gov/pubmed/37025268 http://dx.doi.org/10.3389/fsurg.2023.1141857 |
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