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Oligodendroglioma Arising in Mature Cystic Teratoma

Background. Development of neuroepithelial tumors from mature cystic teratoma is very rare. We present a case of oligodendroglioma developing inside mature cystic teratoma. Case. Eighteen-years-old female, right adnexal mass with solid and cystic areas was detected. Sections showed all three germ la...

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Detalles Bibliográficos
Autores principales: Ünal, Betül, Güleç, Faruk, Şedele, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976788/
https://www.ncbi.nlm.nih.gov/pubmed/24744929
http://dx.doi.org/10.1155/2014/745462
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author Ünal, Betül
Güleç, Faruk
Şedele, Murat
author_facet Ünal, Betül
Güleç, Faruk
Şedele, Murat
author_sort Ünal, Betül
collection PubMed
description Background. Development of neuroepithelial tumors from mature cystic teratoma is very rare. We present a case of oligodendroglioma developing inside mature cystic teratoma. Case. Eighteen-years-old female, right adnexal mass with solid and cystic areas was detected. Sections showed all three germ layers. Also, a tumoral lesion was observed in a glial fibrillary matrix. Tumor was composed of monotonous, uniform cells which have oval-round nucleus, perinuclear halo, and indistinct cytoplasm. GFAP, EGFR, P53 were positive. Conclusions. We diagnosed oligodendroglioma arising from mature cystic teratoma. There was no recurrence at the end of 13 months followup. The number of cases which have been reported in the literature is only a few.
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spelling pubmed-39767882014-04-17 Oligodendroglioma Arising in Mature Cystic Teratoma Ünal, Betül Güleç, Faruk Şedele, Murat Case Rep Oncol Med Case Report Background. Development of neuroepithelial tumors from mature cystic teratoma is very rare. We present a case of oligodendroglioma developing inside mature cystic teratoma. Case. Eighteen-years-old female, right adnexal mass with solid and cystic areas was detected. Sections showed all three germ layers. Also, a tumoral lesion was observed in a glial fibrillary matrix. Tumor was composed of monotonous, uniform cells which have oval-round nucleus, perinuclear halo, and indistinct cytoplasm. GFAP, EGFR, P53 were positive. Conclusions. We diagnosed oligodendroglioma arising from mature cystic teratoma. There was no recurrence at the end of 13 months followup. The number of cases which have been reported in the literature is only a few. Hindawi Publishing Corporation 2014 2014-03-16 /pmc/articles/PMC3976788/ /pubmed/24744929 http://dx.doi.org/10.1155/2014/745462 Text en Copyright © 2014 Betül Ünal et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ünal, Betül
Güleç, Faruk
Şedele, Murat
Oligodendroglioma Arising in Mature Cystic Teratoma
title Oligodendroglioma Arising in Mature Cystic Teratoma
title_full Oligodendroglioma Arising in Mature Cystic Teratoma
title_fullStr Oligodendroglioma Arising in Mature Cystic Teratoma
title_full_unstemmed Oligodendroglioma Arising in Mature Cystic Teratoma
title_short Oligodendroglioma Arising in Mature Cystic Teratoma
title_sort oligodendroglioma arising in mature cystic teratoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976788/
https://www.ncbi.nlm.nih.gov/pubmed/24744929
http://dx.doi.org/10.1155/2014/745462
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