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The histological representativeness of glioblastoma tissue samples
BACKGROUND: Glioblastomas (GBMs) are known for having a vastly heterogenous histopathology. Several studies have shown that GBMs can be histologically undergraded due to sampling errors of small tissue samples. We sought to explore to what extent histological features in GBMs are dependent on the am...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195928/ https://www.ncbi.nlm.nih.gov/pubmed/33085022 http://dx.doi.org/10.1007/s00701-020-04608-y |
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author | Mikkelsen, Vilde Elisabeth Solheim, Ole Salvesen, Øyvind Torp, Sverre Helge |
author_facet | Mikkelsen, Vilde Elisabeth Solheim, Ole Salvesen, Øyvind Torp, Sverre Helge |
author_sort | Mikkelsen, Vilde Elisabeth |
collection | PubMed |
description | BACKGROUND: Glioblastomas (GBMs) are known for having a vastly heterogenous histopathology. Several studies have shown that GBMs can be histologically undergraded due to sampling errors of small tissue samples. We sought to explore to what extent histological features in GBMs are dependent on the amount of viable tissue on routine slides from both biopsied and resected tumors. METHODS: In 106 newly diagnosed GBM patients, we investigated associations between the presence or degree of 24 histopathological and two immunohistochemical features and the tissue amount on hematoxylin-eosin (HE) slides. The amount of viable tissue was semiquantitatively categorized as “sparse,” “medium,” or “substantial” for each case. Tissue amount was also assessed for associations with MRI volumetrics and the type of surgical procedure. RESULTS: About half (46%) of the assessed histological and immunohistochemical features were significantly associated with tissue amount. The significant features were less present or of a lesser degree when the tissue amount was smaller. Among the significant features were most of the features relevant for diffuse astrocytic tumor grading, i.e., small necroses, palisades, microvascular proliferation, atypia, mitotic count, and Ki-67/MIB-1 proliferative index (PI). CONCLUSION: A substantial proportion of the assessed histological features were at risk of being underrepresented when the amount of viable tissue on HE slides was limited. Most of the grading features were dependent on tissue amount, which underlines the importance of considering sampling errors in diffuse astrocytic tumor grading. Our findings also highlight the importance of adequate tissue collection to increase the quality of diagnostics and histological research. |
format | Online Article Text |
id | pubmed-8195928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-81959282021-06-28 The histological representativeness of glioblastoma tissue samples Mikkelsen, Vilde Elisabeth Solheim, Ole Salvesen, Øyvind Torp, Sverre Helge Acta Neurochir (Wien) Original Article - Tumor - Glioma BACKGROUND: Glioblastomas (GBMs) are known for having a vastly heterogenous histopathology. Several studies have shown that GBMs can be histologically undergraded due to sampling errors of small tissue samples. We sought to explore to what extent histological features in GBMs are dependent on the amount of viable tissue on routine slides from both biopsied and resected tumors. METHODS: In 106 newly diagnosed GBM patients, we investigated associations between the presence or degree of 24 histopathological and two immunohistochemical features and the tissue amount on hematoxylin-eosin (HE) slides. The amount of viable tissue was semiquantitatively categorized as “sparse,” “medium,” or “substantial” for each case. Tissue amount was also assessed for associations with MRI volumetrics and the type of surgical procedure. RESULTS: About half (46%) of the assessed histological and immunohistochemical features were significantly associated with tissue amount. The significant features were less present or of a lesser degree when the tissue amount was smaller. Among the significant features were most of the features relevant for diffuse astrocytic tumor grading, i.e., small necroses, palisades, microvascular proliferation, atypia, mitotic count, and Ki-67/MIB-1 proliferative index (PI). CONCLUSION: A substantial proportion of the assessed histological features were at risk of being underrepresented when the amount of viable tissue on HE slides was limited. Most of the grading features were dependent on tissue amount, which underlines the importance of considering sampling errors in diffuse astrocytic tumor grading. Our findings also highlight the importance of adequate tissue collection to increase the quality of diagnostics and histological research. Springer Vienna 2020-10-21 2021 /pmc/articles/PMC8195928/ /pubmed/33085022 http://dx.doi.org/10.1007/s00701-020-04608-y Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article - Tumor - Glioma Mikkelsen, Vilde Elisabeth Solheim, Ole Salvesen, Øyvind Torp, Sverre Helge The histological representativeness of glioblastoma tissue samples |
title | The histological representativeness of glioblastoma tissue samples |
title_full | The histological representativeness of glioblastoma tissue samples |
title_fullStr | The histological representativeness of glioblastoma tissue samples |
title_full_unstemmed | The histological representativeness of glioblastoma tissue samples |
title_short | The histological representativeness of glioblastoma tissue samples |
title_sort | histological representativeness of glioblastoma tissue samples |
topic | Original Article - Tumor - Glioma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195928/ https://www.ncbi.nlm.nih.gov/pubmed/33085022 http://dx.doi.org/10.1007/s00701-020-04608-y |
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