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A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle

Atypical teratoid rhabdoid tumour (ATRT) is a rare malignant tumour of the central nervous system with embryonal roots. The majority are seen in early childhood and location is often in the posterior fossa. Surgery, radiotherapy and chemotherapy are used in treatment. Knowledge of the localisation o...

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Autores principales: Öztürk, Mehmet, Siğirci, Ahmet, Karadağ, Neşe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659804/
https://www.ncbi.nlm.nih.gov/pubmed/26636017
http://dx.doi.org/10.1186/s40064-015-1526-1
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author Öztürk, Mehmet
Siğirci, Ahmet
Karadağ, Neşe
author_facet Öztürk, Mehmet
Siğirci, Ahmet
Karadağ, Neşe
author_sort Öztürk, Mehmet
collection PubMed
description Atypical teratoid rhabdoid tumour (ATRT) is a rare malignant tumour of the central nervous system with embryonal roots. The majority are seen in early childhood and location is often in the posterior fossa. Surgery, radiotherapy and chemotherapy are used in treatment. Knowledge of the localisation of the mass preoperatively is necessary for direction of the chemoradiotherapy and sufficient resection in surgery. Differentiation from other brain tumours is important because of poor prognosis and differences in treatment. In this paper it was aimed to present the clinical and radiological findings of an ATRT located in the cerebellopontine angle, which occurred with facial paralysis.
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spelling pubmed-46598042015-12-03 A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle Öztürk, Mehmet Siğirci, Ahmet Karadağ, Neşe Springerplus Case Study Atypical teratoid rhabdoid tumour (ATRT) is a rare malignant tumour of the central nervous system with embryonal roots. The majority are seen in early childhood and location is often in the posterior fossa. Surgery, radiotherapy and chemotherapy are used in treatment. Knowledge of the localisation of the mass preoperatively is necessary for direction of the chemoradiotherapy and sufficient resection in surgery. Differentiation from other brain tumours is important because of poor prognosis and differences in treatment. In this paper it was aimed to present the clinical and radiological findings of an ATRT located in the cerebellopontine angle, which occurred with facial paralysis. Springer International Publishing 2015-11-25 /pmc/articles/PMC4659804/ /pubmed/26636017 http://dx.doi.org/10.1186/s40064-015-1526-1 Text en © Öztürk et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Study
Öztürk, Mehmet
Siğirci, Ahmet
Karadağ, Neşe
A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title_full A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title_fullStr A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title_full_unstemmed A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title_short A rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
title_sort rare cause of infant facial paralysis: atypical teratoid rhabdoid tumour located in the cerebellopontine angle
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659804/
https://www.ncbi.nlm.nih.gov/pubmed/26636017
http://dx.doi.org/10.1186/s40064-015-1526-1
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