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Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases

INTRODUCTION: Spinal lipoma and spinal arteriovenous fistula (sAVF) are different pathologies and their co-existence is extremely rare. Here we reported two cases of adult-onset sAVF occurring within a spinal lipoma and with review the literature in an attempt to identify the mechanisim of and optim...

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Autores principales: Horiuchi, Yosuke, Iwanami, Akio, Akiyama, Takenori, Hikata, Tomohiro, Watanabe, Kota, Yagi, Mitsuru, Fujita, Nobuyuki, Okada, Eijiro, Nagoshi, Narihito, Tsuji, Osahiko, Ishii, Ken, Yoshida, Kazunari, Nakamura, Masaya, Matsumoto, Morio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798916/
https://www.ncbi.nlm.nih.gov/pubmed/29423285
http://dx.doi.org/10.1038/s41394-017-0011-1
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author Horiuchi, Yosuke
Iwanami, Akio
Akiyama, Takenori
Hikata, Tomohiro
Watanabe, Kota
Yagi, Mitsuru
Fujita, Nobuyuki
Okada, Eijiro
Nagoshi, Narihito
Tsuji, Osahiko
Ishii, Ken
Yoshida, Kazunari
Nakamura, Masaya
Matsumoto, Morio
author_facet Horiuchi, Yosuke
Iwanami, Akio
Akiyama, Takenori
Hikata, Tomohiro
Watanabe, Kota
Yagi, Mitsuru
Fujita, Nobuyuki
Okada, Eijiro
Nagoshi, Narihito
Tsuji, Osahiko
Ishii, Ken
Yoshida, Kazunari
Nakamura, Masaya
Matsumoto, Morio
author_sort Horiuchi, Yosuke
collection PubMed
description INTRODUCTION: Spinal lipoma and spinal arteriovenous fistula (sAVF) are different pathologies and their co-existence is extremely rare. Here we reported two cases of adult-onset sAVF occurring within a spinal lipoma and with review the literature in an attempt to identify the mechanisim of and optimal treatment of this condition. CASE PRESENTATION: Case 1 was a 51-year-old man who was treated by embolization of the feeding artery and ligation of the draining vein. Case 2 was a 53-year-old man who was treated by embolization and resection of the tumor containing the shunt zone. In both cases, symptoms improved after surgery. However, in Case 1, angiography at 1 month after the surgery revealed recurrence of the arteriovenous shunt. DISCUSSION: A literature search revealed only nine other similar case reports. All cases, including ours occurred in adults. In almost all cases, the shunt was located within the spinal lipoma. Pathologic examination revealed venous hypertension, but no evidence of congenital vascular malformation. Given that lipomas release angiogenic factors, the presence of a spinal lipoma may indicate its involvement in the development of acquired sAVF. Our two cases might represent a new subtype of sAVF. Based on our experiences, we recommend resection of the tumor containing the shunt for the management of sAVF.
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spelling pubmed-57989162018-02-23 Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases Horiuchi, Yosuke Iwanami, Akio Akiyama, Takenori Hikata, Tomohiro Watanabe, Kota Yagi, Mitsuru Fujita, Nobuyuki Okada, Eijiro Nagoshi, Narihito Tsuji, Osahiko Ishii, Ken Yoshida, Kazunari Nakamura, Masaya Matsumoto, Morio Spinal Cord Ser Cases Case Report INTRODUCTION: Spinal lipoma and spinal arteriovenous fistula (sAVF) are different pathologies and their co-existence is extremely rare. Here we reported two cases of adult-onset sAVF occurring within a spinal lipoma and with review the literature in an attempt to identify the mechanisim of and optimal treatment of this condition. CASE PRESENTATION: Case 1 was a 51-year-old man who was treated by embolization of the feeding artery and ligation of the draining vein. Case 2 was a 53-year-old man who was treated by embolization and resection of the tumor containing the shunt zone. In both cases, symptoms improved after surgery. However, in Case 1, angiography at 1 month after the surgery revealed recurrence of the arteriovenous shunt. DISCUSSION: A literature search revealed only nine other similar case reports. All cases, including ours occurred in adults. In almost all cases, the shunt was located within the spinal lipoma. Pathologic examination revealed venous hypertension, but no evidence of congenital vascular malformation. Given that lipomas release angiogenic factors, the presence of a spinal lipoma may indicate its involvement in the development of acquired sAVF. Our two cases might represent a new subtype of sAVF. Based on our experiences, we recommend resection of the tumor containing the shunt for the management of sAVF. Nature Publishing Group UK 2017-11-14 /pmc/articles/PMC5798916/ /pubmed/29423285 http://dx.doi.org/10.1038/s41394-017-0011-1 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Horiuchi, Yosuke
Iwanami, Akio
Akiyama, Takenori
Hikata, Tomohiro
Watanabe, Kota
Yagi, Mitsuru
Fujita, Nobuyuki
Okada, Eijiro
Nagoshi, Narihito
Tsuji, Osahiko
Ishii, Ken
Yoshida, Kazunari
Nakamura, Masaya
Matsumoto, Morio
Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title_full Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title_fullStr Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title_full_unstemmed Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title_short Spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
title_sort spinal arteriovenous fistula coexisting within a spinal lipoma: report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798916/
https://www.ncbi.nlm.nih.gov/pubmed/29423285
http://dx.doi.org/10.1038/s41394-017-0011-1
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