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Supratentorial endodermal cysts - Report of two cases
We describe two rare cases of frontal cystic lesions presenting with symptoms and signs of raised intracranial pressure. Both had a preoperative diagnosis of an arachnoid cyst and were subjected to a craniotomy with marsupialization of the cyst. However, the histology confirmed them to be an endoder...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849309/ https://www.ncbi.nlm.nih.gov/pubmed/27366267 http://dx.doi.org/10.4103/1793-5482.179642 |
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author | Rangarajan, Vithal Mahore, Amit Patil, Manoj Kashinath Shendarkar, Ashwini Dnyandaevrao |
author_facet | Rangarajan, Vithal Mahore, Amit Patil, Manoj Kashinath Shendarkar, Ashwini Dnyandaevrao |
author_sort | Rangarajan, Vithal |
collection | PubMed |
description | We describe two rare cases of frontal cystic lesions presenting with symptoms and signs of raised intracranial pressure. Both had a preoperative diagnosis of an arachnoid cyst and were subjected to a craniotomy with marsupialization of the cyst. However, the histology confirmed them to be an endodermal cyst (EC) on both occasions. Both the patients have been closely followed with no recurrence of symptoms. ECs of the central nervous system are usually reported in the spinal canal, mid-line posterior fossa, and the suprasellar regions. Supratentorial and non-midline ECs are rare, with only about 22 cases previously reported in literature. We discuss both the cases and review the relevant literature. |
format | Online Article Text |
id | pubmed-4849309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48493092016-07-01 Supratentorial endodermal cysts - Report of two cases Rangarajan, Vithal Mahore, Amit Patil, Manoj Kashinath Shendarkar, Ashwini Dnyandaevrao Asian J Neurosurg Case Report We describe two rare cases of frontal cystic lesions presenting with symptoms and signs of raised intracranial pressure. Both had a preoperative diagnosis of an arachnoid cyst and were subjected to a craniotomy with marsupialization of the cyst. However, the histology confirmed them to be an endodermal cyst (EC) on both occasions. Both the patients have been closely followed with no recurrence of symptoms. ECs of the central nervous system are usually reported in the spinal canal, mid-line posterior fossa, and the suprasellar regions. Supratentorial and non-midline ECs are rare, with only about 22 cases previously reported in literature. We discuss both the cases and review the relevant literature. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4849309/ /pubmed/27366267 http://dx.doi.org/10.4103/1793-5482.179642 Text en Copyright: © 2016 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Rangarajan, Vithal Mahore, Amit Patil, Manoj Kashinath Shendarkar, Ashwini Dnyandaevrao Supratentorial endodermal cysts - Report of two cases |
title | Supratentorial endodermal cysts - Report of two cases |
title_full | Supratentorial endodermal cysts - Report of two cases |
title_fullStr | Supratentorial endodermal cysts - Report of two cases |
title_full_unstemmed | Supratentorial endodermal cysts - Report of two cases |
title_short | Supratentorial endodermal cysts - Report of two cases |
title_sort | supratentorial endodermal cysts - report of two cases |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849309/ https://www.ncbi.nlm.nih.gov/pubmed/27366267 http://dx.doi.org/10.4103/1793-5482.179642 |
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