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Adult intramedullary epidermoid cyst without spinal dysraphism: A case report

BACKGROUND: Intramedullary epidermoid cyst (IEC), typically associated with spinal dysraphism, is rare, with fewer than 80 such cases reported in the literature. Here we present an adult with an IEC without spinal dysraphism. CASE DESCRIPTION: A 41-year-old female presented with the gradual onset of...

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Autores principales: Mishra, Ajit M., Prabhuraj, A. R., Pruthi, Nupur, Rao, Shilpa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024502/
https://www.ncbi.nlm.nih.gov/pubmed/30009086
http://dx.doi.org/10.4103/sni.sni_117_18
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author Mishra, Ajit M.
Prabhuraj, A. R.
Pruthi, Nupur
Rao, Shilpa
author_facet Mishra, Ajit M.
Prabhuraj, A. R.
Pruthi, Nupur
Rao, Shilpa
author_sort Mishra, Ajit M.
collection PubMed
description BACKGROUND: Intramedullary epidermoid cyst (IEC), typically associated with spinal dysraphism, is rare, with fewer than 80 such cases reported in the literature. Here we present an adult with an IEC without spinal dysraphism. CASE DESCRIPTION: A 41-year-old female presented with the gradual onset of a progressive spastic paraparesis attributed to a magnetic resonance imaging (MRI)-documented D8-9 intramedullary lesion. Following microsurgical excision of the IEC, she fully recovered. CONCLUSION: IECs are rare lesions, typically found in conjunction with spinal dysraphism. Utilizing MRI studies to document the lesion location, gross total microsurgical excision is the procedure of choice. Early excision of these benign lesions maximizes functional recovery.
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spelling pubmed-60245022018-07-13 Adult intramedullary epidermoid cyst without spinal dysraphism: A case report Mishra, Ajit M. Prabhuraj, A. R. Pruthi, Nupur Rao, Shilpa Surg Neurol Int Spine: Case Report BACKGROUND: Intramedullary epidermoid cyst (IEC), typically associated with spinal dysraphism, is rare, with fewer than 80 such cases reported in the literature. Here we present an adult with an IEC without spinal dysraphism. CASE DESCRIPTION: A 41-year-old female presented with the gradual onset of a progressive spastic paraparesis attributed to a magnetic resonance imaging (MRI)-documented D8-9 intramedullary lesion. Following microsurgical excision of the IEC, she fully recovered. CONCLUSION: IECs are rare lesions, typically found in conjunction with spinal dysraphism. Utilizing MRI studies to document the lesion location, gross total microsurgical excision is the procedure of choice. Early excision of these benign lesions maximizes functional recovery. Medknow Publications & Media Pvt Ltd 2018-06-18 /pmc/articles/PMC6024502/ /pubmed/30009086 http://dx.doi.org/10.4103/sni.sni_117_18 Text en Copyright: © 2018 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Spine: Case Report
Mishra, Ajit M.
Prabhuraj, A. R.
Pruthi, Nupur
Rao, Shilpa
Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title_full Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title_fullStr Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title_full_unstemmed Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title_short Adult intramedullary epidermoid cyst without spinal dysraphism: A case report
title_sort adult intramedullary epidermoid cyst without spinal dysraphism: a case report
topic Spine: Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024502/
https://www.ncbi.nlm.nih.gov/pubmed/30009086
http://dx.doi.org/10.4103/sni.sni_117_18
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