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Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case
Pilocytic astrocytomas (PAs) are World Heath Organization Grade I tumors and are most common in children. PA calcification is not a common finding and has been reported more frequently in the optic nerve, hypothalamic/thalamus and superficially located cerebral tumors. We present a cerebellar PA in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Neurosurgical Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028618/ https://www.ncbi.nlm.nih.gov/pubmed/27651876 http://dx.doi.org/10.3340/jkns.2016.59.5.533 |
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author | Aydemir, Fatih Kardes, Ozgur Kayaselçuk, Fazilet Tufan, Kadir |
author_facet | Aydemir, Fatih Kardes, Ozgur Kayaselçuk, Fazilet Tufan, Kadir |
author_sort | Aydemir, Fatih |
collection | PubMed |
description | Pilocytic astrocytomas (PAs) are World Heath Organization Grade I tumors and are most common in children. PA calcification is not a common finding and has been reported more frequently in the optic nerve, hypothalamic/thalamus and superficially located cerebral tumors. We present a cerebellar PA in a 3-year-old male patient with cystic components and massive calcification areas. The residual tumor grew rapidly after the first operation, and the patient was operated on again. A histopathological examination revealed polar spongioblastoma-like cells. Massive calcification is not a common feature in PAs and can lead to difficulties in radiological and pathological differential diagnoses. |
format | Online Article Text |
id | pubmed-5028618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Neurosurgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50286182016-09-20 Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case Aydemir, Fatih Kardes, Ozgur Kayaselçuk, Fazilet Tufan, Kadir J Korean Neurosurg Soc Case Report Pilocytic astrocytomas (PAs) are World Heath Organization Grade I tumors and are most common in children. PA calcification is not a common finding and has been reported more frequently in the optic nerve, hypothalamic/thalamus and superficially located cerebral tumors. We present a cerebellar PA in a 3-year-old male patient with cystic components and massive calcification areas. The residual tumor grew rapidly after the first operation, and the patient was operated on again. A histopathological examination revealed polar spongioblastoma-like cells. Massive calcification is not a common feature in PAs and can lead to difficulties in radiological and pathological differential diagnoses. The Korean Neurosurgical Society 2016-09 2016-09-08 /pmc/articles/PMC5028618/ /pubmed/27651876 http://dx.doi.org/10.3340/jkns.2016.59.5.533 Text en Copyright © 2016 The Korean Neurosurgical Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Aydemir, Fatih Kardes, Ozgur Kayaselçuk, Fazilet Tufan, Kadir Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title | Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title_full | Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title_fullStr | Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title_full_unstemmed | Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title_short | Massive Calcified Cerebellar Pilocytic Astrocytoma with Rapid Recurrence : A Rare Case |
title_sort | massive calcified cerebellar pilocytic astrocytoma with rapid recurrence : a rare case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028618/ https://www.ncbi.nlm.nih.gov/pubmed/27651876 http://dx.doi.org/10.3340/jkns.2016.59.5.533 |
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