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Chiari type I malformation with occult tethered cord syndrome in a child: A case report
RATIONALE: Chiari type I malformation (CM1) and occult tethered cord syndrome (OTCS) are considered to be malformations associated with subtle structural abnormalities of the terminal filum. Few studies have reported patients with CM1 and OTCS. Treatment strategy for patients of CM1 associated with...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738018/ https://www.ncbi.nlm.nih.gov/pubmed/28984782 http://dx.doi.org/10.1097/MD.0000000000008239 |
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author | Zhou, Yuan Zhu, Lin Lin, Yixing Cheng, Huilin |
author_facet | Zhou, Yuan Zhu, Lin Lin, Yixing Cheng, Huilin |
author_sort | Zhou, Yuan |
collection | PubMed |
description | RATIONALE: Chiari type I malformation (CM1) and occult tethered cord syndrome (OTCS) are considered to be malformations associated with subtle structural abnormalities of the terminal filum. Few studies have reported patients with CM1 and OTCS. Treatment strategy for patients of CM1 associated with OTCS is controversial. PATIENT CONCERNS: A 14-year-old child was admitted with intermittent pain and numbness in the right upper limb. And he had urinary frequency, neck pain, back pain, and numbness simultaneously. The imaging examinations showed CM1, syringomyelia, small fat in the filum at the level of the L2 vertebral body but the conus medullaris at the aspect of the L1 vertebral body. DIAGNOSES: The child was diagnosed with CM1 associated with OTCS. INTERVENTIONS: Patient underwent sectioning of filum terminale (SFT) under electrophysiological monitoring during the first hospital and posterior fossa decompression (PFD) during the second hospital. OUTCOMES: After first discharge pain of the right upper limb was relieved, but he still felt numbness. And his numbness was relieved after second discharge. The imaging examinations also showed corresponding improvement during the 2-year follow-up period. LESSONS: For pediatric patients with CM1 and TCS, treatment trouble is not only to choose the staging operation or simultaneous operation but also staging procedures for treatment of 2 lesions. Detailed preoperative evaluation is essential for development of individualized surgical plan. Staging operation of firstly minimally invasive SFT and later PFD may be helpful for such cases owing to its positive effect on both the symptoms and imaging findings. |
format | Online Article Text |
id | pubmed-5738018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-57380182018-01-02 Chiari type I malformation with occult tethered cord syndrome in a child: A case report Zhou, Yuan Zhu, Lin Lin, Yixing Cheng, Huilin Medicine (Baltimore) 7100 RATIONALE: Chiari type I malformation (CM1) and occult tethered cord syndrome (OTCS) are considered to be malformations associated with subtle structural abnormalities of the terminal filum. Few studies have reported patients with CM1 and OTCS. Treatment strategy for patients of CM1 associated with OTCS is controversial. PATIENT CONCERNS: A 14-year-old child was admitted with intermittent pain and numbness in the right upper limb. And he had urinary frequency, neck pain, back pain, and numbness simultaneously. The imaging examinations showed CM1, syringomyelia, small fat in the filum at the level of the L2 vertebral body but the conus medullaris at the aspect of the L1 vertebral body. DIAGNOSES: The child was diagnosed with CM1 associated with OTCS. INTERVENTIONS: Patient underwent sectioning of filum terminale (SFT) under electrophysiological monitoring during the first hospital and posterior fossa decompression (PFD) during the second hospital. OUTCOMES: After first discharge pain of the right upper limb was relieved, but he still felt numbness. And his numbness was relieved after second discharge. The imaging examinations also showed corresponding improvement during the 2-year follow-up period. LESSONS: For pediatric patients with CM1 and TCS, treatment trouble is not only to choose the staging operation or simultaneous operation but also staging procedures for treatment of 2 lesions. Detailed preoperative evaluation is essential for development of individualized surgical plan. Staging operation of firstly minimally invasive SFT and later PFD may be helpful for such cases owing to its positive effect on both the symptoms and imaging findings. Wolters Kluwer Health 2017-10-27 /pmc/articles/PMC5738018/ /pubmed/28984782 http://dx.doi.org/10.1097/MD.0000000000008239 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 7100 Zhou, Yuan Zhu, Lin Lin, Yixing Cheng, Huilin Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title | Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title_full | Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title_fullStr | Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title_full_unstemmed | Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title_short | Chiari type I malformation with occult tethered cord syndrome in a child: A case report |
title_sort | chiari type i malformation with occult tethered cord syndrome in a child: a case report |
topic | 7100 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738018/ https://www.ncbi.nlm.nih.gov/pubmed/28984782 http://dx.doi.org/10.1097/MD.0000000000008239 |
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