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Dermoid cyst: A rare intramedullary inclusion cyst

Intramedullary dermoid cysts are rare tumors, especially those not associated with spinal dysraphism. Only six cases have been reported in the literature. Of these, only two cases have had magnetic resonance imaging studies. We report a case of an 18-year-old female patient, who presented with progr...

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Detalles Bibliográficos
Autores principales: Patankar, A. P., Sheth, J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410166/
https://www.ncbi.nlm.nih.gov/pubmed/22870157
http://dx.doi.org/10.4103/1793-5482.98651
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author Patankar, A. P.
Sheth, J. H.
author_facet Patankar, A. P.
Sheth, J. H.
author_sort Patankar, A. P.
collection PubMed
description Intramedullary dermoid cysts are rare tumors, especially those not associated with spinal dysraphism. Only six cases have been reported in the literature. Of these, only two cases have had magnetic resonance imaging studies. We report a case of an 18-year-old female patient, who presented with progressive weakness of both the lower limbs and wasting of both the upper limbs. Magnetic resonance imaging (MRI) showed an intramedullary lesion extending from C3 to D2 with peripheral enhancement on contrast. Decompression of the cystic contents with partial removal of cyst wall was done. Hair with oily cholesterol and keratin debris was encountered. Histopathology confirmed the diagnosis of dermoid cyst. This case adds to the previous reported cases of the rare and uncommon intramedullary space occupying lesions of the spinal cord.
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spelling pubmed-34101662012-08-06 Dermoid cyst: A rare intramedullary inclusion cyst Patankar, A. P. Sheth, J. H. Asian J Neurosurg Case Report Intramedullary dermoid cysts are rare tumors, especially those not associated with spinal dysraphism. Only six cases have been reported in the literature. Of these, only two cases have had magnetic resonance imaging studies. We report a case of an 18-year-old female patient, who presented with progressive weakness of both the lower limbs and wasting of both the upper limbs. Magnetic resonance imaging (MRI) showed an intramedullary lesion extending from C3 to D2 with peripheral enhancement on contrast. Decompression of the cystic contents with partial removal of cyst wall was done. Hair with oily cholesterol and keratin debris was encountered. Histopathology confirmed the diagnosis of dermoid cyst. This case adds to the previous reported cases of the rare and uncommon intramedullary space occupying lesions of the spinal cord. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3410166/ /pubmed/22870157 http://dx.doi.org/10.4103/1793-5482.98651 Text en Copyright: © Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Patankar, A. P.
Sheth, J. H.
Dermoid cyst: A rare intramedullary inclusion cyst
title Dermoid cyst: A rare intramedullary inclusion cyst
title_full Dermoid cyst: A rare intramedullary inclusion cyst
title_fullStr Dermoid cyst: A rare intramedullary inclusion cyst
title_full_unstemmed Dermoid cyst: A rare intramedullary inclusion cyst
title_short Dermoid cyst: A rare intramedullary inclusion cyst
title_sort dermoid cyst: a rare intramedullary inclusion cyst
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410166/
https://www.ncbi.nlm.nih.gov/pubmed/22870157
http://dx.doi.org/10.4103/1793-5482.98651
work_keys_str_mv AT patankarap dermoidcystarareintramedullaryinclusioncyst
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