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Cerebral gliosarcoma with perivascular involvement in a cat
CASE SUMMARY: A 5-year-old neutered male domestic shorthair cat presented with an 18-month history of facial tics, and progressive general ataxia, weakness, lethargy and anorexia of 2 weeks’ duration. MRI of the brain showed a well-defined heterogeneous hyperintense mass on T1-weighted and T2-weight...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787989/ https://www.ncbi.nlm.nih.gov/pubmed/31636916 http://dx.doi.org/10.1177/2055116919879783 |
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author | Álvarez, Patricia Wessmann, Annette Pascual, Mireia Comas, Oriol Pi, Dolors Pumarola, Martí |
author_facet | Álvarez, Patricia Wessmann, Annette Pascual, Mireia Comas, Oriol Pi, Dolors Pumarola, Martí |
author_sort | Álvarez, Patricia |
collection | PubMed |
description | CASE SUMMARY: A 5-year-old neutered male domestic shorthair cat presented with an 18-month history of facial tics, and progressive general ataxia, weakness, lethargy and anorexia of 2 weeks’ duration. MRI of the brain showed a well-defined heterogeneous hyperintense mass on T1-weighted and T2-weighted images, with central hypointensity in the rostral commissure and septum pellucidum, and perilesional hyperintensity in fluid-attenuated inversion recovery, suggestive of perilesional oedema. Gross examination in a transverse section of the brain at the level of the septum pellucidum revealed a 0.2 cm brown soft mass. Histopathological examination identified a biphasic neoplastic proliferation of mesenchymal and neuroepithelial cell populations. Fusiform cells were predominately distributed in bundles showing a high degree of anisocytosis and marked immune-positive reaction to vimentin immunochemistry, confirming a sarcomatous origin. Additionally, high numbers of astrocytic cells were identified by an intense immunopositive reaction to glial fibrillary acidic protein and negative reaction to oligodendrocyte transcription factor 2 immunochemistry. Vascular invasion of the neoplasia into the wall of a medium branch of the rostral cerebral artery was present (secondary Scherer structures). Based on these characteristics, the tumour was defined as a gliosarcoma. Gliosarcoma is a recognised astrocytoma grade IV anaplastic glial cell tumour with sarcomatous differentiation. RELEVANCE AND NOVEL INFORMATION: To our knowledge, this is the first report describing a cerebral gliosarcoma in a cat including clinical, MRI, macroscopic and histopathological features and immunolabelling characteristics. |
format | Online Article Text |
id | pubmed-6787989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67879892019-10-21 Cerebral gliosarcoma with perivascular involvement in a cat Álvarez, Patricia Wessmann, Annette Pascual, Mireia Comas, Oriol Pi, Dolors Pumarola, Martí JFMS Open Rep Case Report CASE SUMMARY: A 5-year-old neutered male domestic shorthair cat presented with an 18-month history of facial tics, and progressive general ataxia, weakness, lethargy and anorexia of 2 weeks’ duration. MRI of the brain showed a well-defined heterogeneous hyperintense mass on T1-weighted and T2-weighted images, with central hypointensity in the rostral commissure and septum pellucidum, and perilesional hyperintensity in fluid-attenuated inversion recovery, suggestive of perilesional oedema. Gross examination in a transverse section of the brain at the level of the septum pellucidum revealed a 0.2 cm brown soft mass. Histopathological examination identified a biphasic neoplastic proliferation of mesenchymal and neuroepithelial cell populations. Fusiform cells were predominately distributed in bundles showing a high degree of anisocytosis and marked immune-positive reaction to vimentin immunochemistry, confirming a sarcomatous origin. Additionally, high numbers of astrocytic cells were identified by an intense immunopositive reaction to glial fibrillary acidic protein and negative reaction to oligodendrocyte transcription factor 2 immunochemistry. Vascular invasion of the neoplasia into the wall of a medium branch of the rostral cerebral artery was present (secondary Scherer structures). Based on these characteristics, the tumour was defined as a gliosarcoma. Gliosarcoma is a recognised astrocytoma grade IV anaplastic glial cell tumour with sarcomatous differentiation. RELEVANCE AND NOVEL INFORMATION: To our knowledge, this is the first report describing a cerebral gliosarcoma in a cat including clinical, MRI, macroscopic and histopathological features and immunolabelling characteristics. SAGE Publications 2019-10-10 /pmc/articles/PMC6787989/ /pubmed/31636916 http://dx.doi.org/10.1177/2055116919879783 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Álvarez, Patricia Wessmann, Annette Pascual, Mireia Comas, Oriol Pi, Dolors Pumarola, Martí Cerebral gliosarcoma with perivascular involvement in a cat |
title | Cerebral gliosarcoma with perivascular involvement in a
cat |
title_full | Cerebral gliosarcoma with perivascular involvement in a
cat |
title_fullStr | Cerebral gliosarcoma with perivascular involvement in a
cat |
title_full_unstemmed | Cerebral gliosarcoma with perivascular involvement in a
cat |
title_short | Cerebral gliosarcoma with perivascular involvement in a
cat |
title_sort | cerebral gliosarcoma with perivascular involvement in a
cat |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787989/ https://www.ncbi.nlm.nih.gov/pubmed/31636916 http://dx.doi.org/10.1177/2055116919879783 |
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