Pilomyxoid astrocytomas: a short review
Pilomyxoid astrocytoma is a variant of pilocytic astrocytoma and the clinical, histological and molecular data point to a very close relationship as well as a more aggressive biological behavior for the former. WHO 2016 classification does not provide a specific grade for these neoplasms, but there...
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Veröffentlicht in: | Brain tumor pathology 2019-04, Vol.36 (2), p.52-55 |
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description | Pilomyxoid astrocytoma is a variant of pilocytic astrocytoma and the clinical, histological and molecular data point to a very close relationship as well as a more aggressive biological behavior for the former. WHO 2016 classification does not provide a specific grade for these neoplasms, but there is sufficient evidence in the literature that pilomyxoid astrocytoma has slightly worse prognosis than typical pilocytic astrocytoma. There is increasing evidence that in addition to the MAPK pathway alterations, pilomyxoid astrocytomas harbor genetic alterations that distinguish them from typical pilocytic astrocytoma |
doi_str_mv | 10.1007/s10014-019-00343-0 |
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WHO 2016 classification does not provide a specific grade for these neoplasms, but there is sufficient evidence in the literature that pilomyxoid astrocytoma has slightly worse prognosis than typical pilocytic astrocytoma. 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WHO 2016 classification does not provide a specific grade for these neoplasms, but there is sufficient evidence in the literature that pilomyxoid astrocytoma has slightly worse prognosis than typical pilocytic astrocytoma. There is increasing evidence that in addition to the MAPK pathway alterations, pilomyxoid astrocytomas harbor genetic alterations that distinguish them from typical pilocytic astrocytoma</description><subject>Cancer Research</subject><subject>Chromosomes</subject><subject>Classification</subject><subject>Genes</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mutation</subject><subject>Nervous system</subject><subject>Neurology</subject><subject>Neurosurgery</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Review Article</subject><subject>Spinal cord</subject><subject>Tumors</subject><issn>1433-7398</issn><issn>1861-387X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kE1LxDAURYMozjj6B1xIwYVuqi8fbRJ3MvgFgi4U3IU0TbVDOxmTVp1_b8aOCi7cJIGce9_jILSP4QQD8NMQT8xSwDIFoIymsIHGWOQ4pYI_bcY3ozTlVIoR2glhBsAYcLyNRhQkywBnY3R0XzeuXX64ukx06Lwzy861OpwlOgkvzneJt2-1fd9FW5Vugt1b3xP0eHnxML1Ob--ubqbnt6mhUnYptxKXrBC20NJWTDOSE5kJXfGC6ZxoVlRQUp7lWUaEloIJaiQzmSCmxKYSdIKOh96Fd6-9DZ1q62Bs0-i5dX1QhADFLMeQRfTwDzpzvZ_H7RSRmEvOhVhRZKCMdyF4W6mFr1vtlwqDWmlUg0YVNaovjQpi6GBd3RetLX8i394iQAcgxK_5s_W_s_-p_QSCSXtI</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Kulac, Ibrahim</creator><creator>Tihan, Tarik</creator><general>Springer Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4551-2555</orcidid></search><sort><creationdate>20190401</creationdate><title>Pilomyxoid astrocytomas: a short review</title><author>Kulac, Ibrahim ; 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subjects | Cancer Research Chromosomes Classification Genes Medical prognosis Medicine Medicine & Public Health Mutation Nervous system Neurology Neurosurgery Oncology Pathology Review Article Spinal cord Tumors |
title | Pilomyxoid astrocytomas: a short review |
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