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Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report

BACKGROUND: Spinal dural arteriovenous fistula (SDAVF) usually occurs during the 4(th) to 6(th) decades of life, and adolescent SDAVF is rarely reported. SDAVF arising around a tumor is also rare, and reported tumors are mostly schwannoma and lipoma. CASE PRESENTATION: We reported a 16-year-old male...

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Autores principales: Chu, Chan-Lin, Lu, Yu-Jen, Lee, Tsong-Hai, Jung, Shih-Ming, Chu, Yu-Cheng, Wong, Ho-Fai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742378/
https://www.ncbi.nlm.nih.gov/pubmed/34998361
http://dx.doi.org/10.1186/s12887-021-03032-0
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author Chu, Chan-Lin
Lu, Yu-Jen
Lee, Tsong-Hai
Jung, Shih-Ming
Chu, Yu-Cheng
Wong, Ho-Fai
author_facet Chu, Chan-Lin
Lu, Yu-Jen
Lee, Tsong-Hai
Jung, Shih-Ming
Chu, Yu-Cheng
Wong, Ho-Fai
author_sort Chu, Chan-Lin
collection PubMed
description BACKGROUND: Spinal dural arteriovenous fistula (SDAVF) usually occurs during the 4(th) to 6(th) decades of life, and adolescent SDAVF is rarely reported. SDAVF arising around a tumor is also rare, and reported tumors are mostly schwannoma and lipoma. CASE PRESENTATION: We reported a 16-year-old male presented with progressive weakness and numbness of lower limbs for 3 months. A SDAVF was found, which was fed by right radicular arteries from segmental artery at L2 level and drained retrogradely into perimedullary veins. A concomitant spinal extradural nodular fasciitis at right L1/L2 intervertebral foramen was also noted. The SDAVF was completely obliterated by endovascular treatment and the tumor was debulked. The patient recovered well after the procedures. CONCLUSIONS: Our case report suggests SDAVF can occur in adolescent. The concomitant presence with a nodular fasciitis indicates that although it usually arises in subcutaneous tissue but can rarely form on the dura of spine.
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spelling pubmed-87423782022-01-10 Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report Chu, Chan-Lin Lu, Yu-Jen Lee, Tsong-Hai Jung, Shih-Ming Chu, Yu-Cheng Wong, Ho-Fai BMC Pediatr Case Report BACKGROUND: Spinal dural arteriovenous fistula (SDAVF) usually occurs during the 4(th) to 6(th) decades of life, and adolescent SDAVF is rarely reported. SDAVF arising around a tumor is also rare, and reported tumors are mostly schwannoma and lipoma. CASE PRESENTATION: We reported a 16-year-old male presented with progressive weakness and numbness of lower limbs for 3 months. A SDAVF was found, which was fed by right radicular arteries from segmental artery at L2 level and drained retrogradely into perimedullary veins. A concomitant spinal extradural nodular fasciitis at right L1/L2 intervertebral foramen was also noted. The SDAVF was completely obliterated by endovascular treatment and the tumor was debulked. The patient recovered well after the procedures. CONCLUSIONS: Our case report suggests SDAVF can occur in adolescent. The concomitant presence with a nodular fasciitis indicates that although it usually arises in subcutaneous tissue but can rarely form on the dura of spine. BioMed Central 2022-01-08 /pmc/articles/PMC8742378/ /pubmed/34998361 http://dx.doi.org/10.1186/s12887-021-03032-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Chu, Chan-Lin
Lu, Yu-Jen
Lee, Tsong-Hai
Jung, Shih-Ming
Chu, Yu-Cheng
Wong, Ho-Fai
Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title_full Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title_fullStr Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title_full_unstemmed Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title_short Concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
title_sort concomitant spinal dural arteriovenous fistula and nodular fasciitis in an adolescent: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742378/
https://www.ncbi.nlm.nih.gov/pubmed/34998361
http://dx.doi.org/10.1186/s12887-021-03032-0
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