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Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review
BACKGROUND: Spinal manipulation therapy (SMT) has been widely used worldwide to treat musculoskeletal diseases, but it can cause serious adverse events. Spinal epidural hematoma (SEH) caused by SMT is a rare emergency that can cause neurological dysfunction. We herein report three cases of SEH after...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362556/ https://www.ncbi.nlm.nih.gov/pubmed/34435018 http://dx.doi.org/10.12998/wjcc.v9.i22.6501 |
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author | Liu, Hua Zhang, Tao Qu, Tao Yang, Cheng-Wei Li, Song-Kai |
author_facet | Liu, Hua Zhang, Tao Qu, Tao Yang, Cheng-Wei Li, Song-Kai |
author_sort | Liu, Hua |
collection | PubMed |
description | BACKGROUND: Spinal manipulation therapy (SMT) has been widely used worldwide to treat musculoskeletal diseases, but it can cause serious adverse events. Spinal epidural hematoma (SEH) caused by SMT is a rare emergency that can cause neurological dysfunction. We herein report three cases of SEH after SMT. CASE SUMMARY: The first case was a 30-year-old woman who experienced neck pain and numbness in both upper limbs immediately after SMT. Her symptoms persisted after 3 d of conservative treatment, and she was admitted to our hospital. Magnetic resonance imaging (MRI) demonstrated an SEH, extending from C6 to C7. The second case was a 55-year-old man with sudden back pain 1 d after SMT, numbness in both lower limbs, an inability to stand or walk, and difficulty urinating. MRI revealed an SEH, extending from T1 to T3. The third case was a 28-year-old man who suddenly developed symptoms of numbness in both lower limbs 4 h after SMT. He was unable to stand or walk and experienced mild back pain. MRI revealed an SEH, extending from T1 to T2. All three patients underwent surgery after failed conservative treatment. The three cases recovered to ASIA grade E on day 5, 1 wk, and day 10 after surgery, respectively. All patients returned to normal after 3 mo of follow-up. CONCLUSION: SEH caused by SMT is very rare, and the condition of each patient should be evaluated in full detail before operation. SEH should be diagnosed immediately and actively treated by surgery. |
format | Online Article Text |
id | pubmed-8362556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-83625562021-08-24 Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review Liu, Hua Zhang, Tao Qu, Tao Yang, Cheng-Wei Li, Song-Kai World J Clin Cases Case Report BACKGROUND: Spinal manipulation therapy (SMT) has been widely used worldwide to treat musculoskeletal diseases, but it can cause serious adverse events. Spinal epidural hematoma (SEH) caused by SMT is a rare emergency that can cause neurological dysfunction. We herein report three cases of SEH after SMT. CASE SUMMARY: The first case was a 30-year-old woman who experienced neck pain and numbness in both upper limbs immediately after SMT. Her symptoms persisted after 3 d of conservative treatment, and she was admitted to our hospital. Magnetic resonance imaging (MRI) demonstrated an SEH, extending from C6 to C7. The second case was a 55-year-old man with sudden back pain 1 d after SMT, numbness in both lower limbs, an inability to stand or walk, and difficulty urinating. MRI revealed an SEH, extending from T1 to T3. The third case was a 28-year-old man who suddenly developed symptoms of numbness in both lower limbs 4 h after SMT. He was unable to stand or walk and experienced mild back pain. MRI revealed an SEH, extending from T1 to T2. All three patients underwent surgery after failed conservative treatment. The three cases recovered to ASIA grade E on day 5, 1 wk, and day 10 after surgery, respectively. All patients returned to normal after 3 mo of follow-up. CONCLUSION: SEH caused by SMT is very rare, and the condition of each patient should be evaluated in full detail before operation. SEH should be diagnosed immediately and actively treated by surgery. Baishideng Publishing Group Inc 2021-08-06 2021-08-06 /pmc/articles/PMC8362556/ /pubmed/34435018 http://dx.doi.org/10.12998/wjcc.v9.i22.6501 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Liu, Hua Zhang, Tao Qu, Tao Yang, Cheng-Wei Li, Song-Kai Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title | Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title_full | Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title_fullStr | Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title_full_unstemmed | Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title_short | Spinal epidural hematoma after spinal manipulation therapy: Report of three cases and a literature review |
title_sort | spinal epidural hematoma after spinal manipulation therapy: report of three cases and a literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8362556/ https://www.ncbi.nlm.nih.gov/pubmed/34435018 http://dx.doi.org/10.12998/wjcc.v9.i22.6501 |
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