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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...

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Autores principales: Agosti, Edoardo, De Maria, Lucio, Panciani, Pier Paolo, Serioli, Simona, Mardighian, Dikran, Fontanella, Marco Maria, Lanzino, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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.
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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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