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Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series

Isocitrate dehydrogenase wild-type (IDHwt) diffuse astrocytomas feature highly infiltrative patterns, such as a gliomatosis cerebri growth pattern with widespread involvement. Among these tumors, localized IDHwt histologically diffuse astrocytomas are rarer than the infiltrative type. The aim of thi...

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Autores principales: Kibe, Yuji, Motomura, Kazuya, Ohka, Fumiharu, Aoki, Kosuke, Shimizu, Hiroyuki, Yamaguchi, Junya, Nishikawa, Tomohide, Saito, Ryuta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842655/
https://www.ncbi.nlm.nih.gov/pubmed/36646712
http://dx.doi.org/10.1038/s41598-022-25928-2
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author Kibe, Yuji
Motomura, Kazuya
Ohka, Fumiharu
Aoki, Kosuke
Shimizu, Hiroyuki
Yamaguchi, Junya
Nishikawa, Tomohide
Saito, Ryuta
author_facet Kibe, Yuji
Motomura, Kazuya
Ohka, Fumiharu
Aoki, Kosuke
Shimizu, Hiroyuki
Yamaguchi, Junya
Nishikawa, Tomohide
Saito, Ryuta
author_sort Kibe, Yuji
collection PubMed
description Isocitrate dehydrogenase wild-type (IDHwt) diffuse astrocytomas feature highly infiltrative patterns, such as a gliomatosis cerebri growth pattern with widespread involvement. Among these tumors, localized IDHwt histologically diffuse astrocytomas are rarer than the infiltrative type. The aim of this study was to assess and describe the clinical, radiographic, histopathological, and molecular characteristics of this rare type of IDHwt histologically diffuse astrocytomas and thereby provide more information on how its features affect clinical prognoses and outcomes. We retrospectively analyzed the records of five patients with localized IDHwt histologically diffuse astrocytomas between July 2017 and January 2020. All patients were female, and their mean age at the time of the initial treatment was 55.0 years. All patients had focal disease that did not include gliomatosis cerebri or multifocal disease. All patients received a histopathological diagnosis of diffuse astrocytomas at the time of the initial treatment. For recurrent tumors, second surgeries were performed at a mean of 12.4 months after the initial surgery. A histopathological diagnosis of glioblastoma was made in four patients and one of gliosarcoma in one patient. The initial status of IDH1, IDH2, H3F3A, HIST1H3B, and BRAF was “wild-type” in all patients. TERT promoter mutations (C250T or C228T) were detected in four patients. No tumors harbored a 1p/19q codeletion, EGFR amplification, or chromosome 7 gain/10 loss (+ 7/ − 10). We assessed clinical cases of localized IDHwt histologically diffuse astrocytomas that resulted in malignant recurrence and a poor clinical prognosis similar to that of glioblastomas. Our case series suggests that even in patients with histologically diffuse astrocytomas and those who present with radiographic imaging findings suggestive of a localized tumor mass, physicians should consider the possibility of IDHwt histologically diffuse astrocytomas.
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spelling pubmed-98426552023-01-18 Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series Kibe, Yuji Motomura, Kazuya Ohka, Fumiharu Aoki, Kosuke Shimizu, Hiroyuki Yamaguchi, Junya Nishikawa, Tomohide Saito, Ryuta Sci Rep Article Isocitrate dehydrogenase wild-type (IDHwt) diffuse astrocytomas feature highly infiltrative patterns, such as a gliomatosis cerebri growth pattern with widespread involvement. Among these tumors, localized IDHwt histologically diffuse astrocytomas are rarer than the infiltrative type. The aim of this study was to assess and describe the clinical, radiographic, histopathological, and molecular characteristics of this rare type of IDHwt histologically diffuse astrocytomas and thereby provide more information on how its features affect clinical prognoses and outcomes. We retrospectively analyzed the records of five patients with localized IDHwt histologically diffuse astrocytomas between July 2017 and January 2020. All patients were female, and their mean age at the time of the initial treatment was 55.0 years. All patients had focal disease that did not include gliomatosis cerebri or multifocal disease. All patients received a histopathological diagnosis of diffuse astrocytomas at the time of the initial treatment. For recurrent tumors, second surgeries were performed at a mean of 12.4 months after the initial surgery. A histopathological diagnosis of glioblastoma was made in four patients and one of gliosarcoma in one patient. The initial status of IDH1, IDH2, H3F3A, HIST1H3B, and BRAF was “wild-type” in all patients. TERT promoter mutations (C250T or C228T) were detected in four patients. No tumors harbored a 1p/19q codeletion, EGFR amplification, or chromosome 7 gain/10 loss (+ 7/ − 10). We assessed clinical cases of localized IDHwt histologically diffuse astrocytomas that resulted in malignant recurrence and a poor clinical prognosis similar to that of glioblastomas. Our case series suggests that even in patients with histologically diffuse astrocytomas and those who present with radiographic imaging findings suggestive of a localized tumor mass, physicians should consider the possibility of IDHwt histologically diffuse astrocytomas. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842655/ /pubmed/36646712 http://dx.doi.org/10.1038/s41598-022-25928-2 Text en © The Author(s) 2022 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 Article
Kibe, Yuji
Motomura, Kazuya
Ohka, Fumiharu
Aoki, Kosuke
Shimizu, Hiroyuki
Yamaguchi, Junya
Nishikawa, Tomohide
Saito, Ryuta
Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title_full Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title_fullStr Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title_full_unstemmed Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title_short Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
title_sort imaging features of localized idh wild-type histologically diffuse astrocytomas: a single-institution case series
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842655/
https://www.ncbi.nlm.nih.gov/pubmed/36646712
http://dx.doi.org/10.1038/s41598-022-25928-2
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