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An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor

Spinal dermoid cysts are rare and account for 0.8% to 1.1% of spinal intramedullary Tumors. Only a few cases of infected spinal dermoid cysts have been reported in the literature and most of them were associated with a dermal sinus as the source of infection. We report a case of an infected spinal d...

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Autores principales: Diyora, Batuk Damjibhai, Bhende, Bhagyashri, Nayak, Naren, Sharma, Alok K.
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/PMC6413619/
https://www.ncbi.nlm.nih.gov/pubmed/30937094
http://dx.doi.org/10.4103/JPN.JPN_34_18
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author Diyora, Batuk Damjibhai
Bhende, Bhagyashri
Nayak, Naren
Sharma, Alok K.
author_facet Diyora, Batuk Damjibhai
Bhende, Bhagyashri
Nayak, Naren
Sharma, Alok K.
author_sort Diyora, Batuk Damjibhai
collection PubMed
description Spinal dermoid cysts are rare and account for 0.8% to 1.1% of spinal intramedullary Tumors. Only a few cases of infected spinal dermoid cysts have been reported in the literature and most of them were associated with a dermal sinus as the source of infection. We report a case of an infected spinal dermoid cyst in the absence of a dermal sinus in a 3-year-old child who underwent excision of cyst. On a long-term follow-up of about 10 years, there was no evidence of any recurrence. However, bowel and bladder dysfunction persisted. In the light of the current literature, we discuss the clinical presentation, etiopathogenesis, radiological features, management, and long-term outcome of an infected conus dermoid cyst.
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spelling pubmed-64136192019-04-01 An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor Diyora, Batuk Damjibhai Bhende, Bhagyashri Nayak, Naren Sharma, Alok K. J Pediatr Neurosci Case Report Spinal dermoid cysts are rare and account for 0.8% to 1.1% of spinal intramedullary Tumors. Only a few cases of infected spinal dermoid cysts have been reported in the literature and most of them were associated with a dermal sinus as the source of infection. We report a case of an infected spinal dermoid cyst in the absence of a dermal sinus in a 3-year-old child who underwent excision of cyst. On a long-term follow-up of about 10 years, there was no evidence of any recurrence. However, bowel and bladder dysfunction persisted. In the light of the current literature, we discuss the clinical presentation, etiopathogenesis, radiological features, management, and long-term outcome of an infected conus dermoid cyst. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6413619/ /pubmed/30937094 http://dx.doi.org/10.4103/JPN.JPN_34_18 Text en Copyright: © 2019 Journal of Pediatric Neurosciences 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 Case Report
Diyora, Batuk Damjibhai
Bhende, Bhagyashri
Nayak, Naren
Sharma, Alok K.
An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title_full An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title_fullStr An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title_full_unstemmed An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title_short An Infected Dermoid Cyst Without a Sinus Tract: A Rarity Mimicking a Spinal Tumor
title_sort infected dermoid cyst without a sinus tract: a rarity mimicking a spinal tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413619/
https://www.ncbi.nlm.nih.gov/pubmed/30937094
http://dx.doi.org/10.4103/JPN.JPN_34_18
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