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Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-ol...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171013/ https://www.ncbi.nlm.nih.gov/pubmed/32314319 http://dx.doi.org/10.1186/s40981-020-00334-7 |
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author | Nakao, Sayo Yamada, Shinichi Tsuda, Katsuya Yokomizo, Taishi Sato, Teruyuki Tanoue, Shuichi Hiraki, Teruyuki |
author_facet | Nakao, Sayo Yamada, Shinichi Tsuda, Katsuya Yokomizo, Taishi Sato, Teruyuki Tanoue, Shuichi Hiraki, Teruyuki |
author_sort | Nakao, Sayo |
collection | PubMed |
description | BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-old woman with SMA type 2. Patients 2 and 3 were 10- and 17-year-old girls with SMA type 1. In patients 1 and 2, the needle was inserted into the spinal column, but outflow of cerebrospinal fluid was unable to be confirmed. CT revealed that the dural sac terminated at the L5 level in patients 1 and 3 and at the L5/S1 level in patient 2. CONCLUSIONS: Patients with SMA often present with high-grade scoliosis, making intrathecal administration difficult. In addition, the dural sac may terminate at a level higher than normal. To ensure intrathecal administration, the level of dural sac termination must be confirmed by CT before puncture. |
format | Online Article Text |
id | pubmed-7171013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-71710132020-04-23 Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity Nakao, Sayo Yamada, Shinichi Tsuda, Katsuya Yokomizo, Taishi Sato, Teruyuki Tanoue, Shuichi Hiraki, Teruyuki JA Clin Rep Case Report BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-old woman with SMA type 2. Patients 2 and 3 were 10- and 17-year-old girls with SMA type 1. In patients 1 and 2, the needle was inserted into the spinal column, but outflow of cerebrospinal fluid was unable to be confirmed. CT revealed that the dural sac terminated at the L5 level in patients 1 and 3 and at the L5/S1 level in patient 2. CONCLUSIONS: Patients with SMA often present with high-grade scoliosis, making intrathecal administration difficult. In addition, the dural sac may terminate at a level higher than normal. To ensure intrathecal administration, the level of dural sac termination must be confirmed by CT before puncture. Springer Berlin Heidelberg 2020-04-20 /pmc/articles/PMC7171013/ /pubmed/32314319 http://dx.doi.org/10.1186/s40981-020-00334-7 Text en © The Author(s) 2020 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/. |
spellingShingle | Case Report Nakao, Sayo Yamada, Shinichi Tsuda, Katsuya Yokomizo, Taishi Sato, Teruyuki Tanoue, Shuichi Hiraki, Teruyuki Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title | Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title_full | Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title_fullStr | Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title_full_unstemmed | Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title_short | Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
title_sort | intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171013/ https://www.ncbi.nlm.nih.gov/pubmed/32314319 http://dx.doi.org/10.1186/s40981-020-00334-7 |
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