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Primary intracranial sarcomas: a clinicopathological investigation

BACKGROUND: The purpose of this study is to present a series of primary intracranial sarcomas (PIS), a rare type of tumor of the central nervous system, in order to improve our understanding of the disease. These tumors are heterogeneous and prone to recurrence after resection, exhibiting a high mor...

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Autores principales: Cai, Yu-Xiang, Liu, Jin-Sheng, Xu, Jian, He, Yong-Ze, Zhang, Huai-Nian, Tian, Su-Fang, Li, Zhi-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288519/
https://www.ncbi.nlm.nih.gov/pubmed/37361584
http://dx.doi.org/10.3389/fonc.2023.1195467
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author Cai, Yu-Xiang
Liu, Jin-Sheng
Xu, Jian
He, Yong-Ze
Zhang, Huai-Nian
Tian, Su-Fang
Li, Zhi-Qiang
author_facet Cai, Yu-Xiang
Liu, Jin-Sheng
Xu, Jian
He, Yong-Ze
Zhang, Huai-Nian
Tian, Su-Fang
Li, Zhi-Qiang
author_sort Cai, Yu-Xiang
collection PubMed
description BACKGROUND: The purpose of this study is to present a series of primary intracranial sarcomas (PIS), a rare type of tumor of the central nervous system, in order to improve our understanding of the disease. These tumors are heterogeneous and prone to recurrence after resection, exhibiting a high mortality rate. As PIS has yet to be understood and studied on a large scale, it is vital for further evaluation and research. METHODS: Our study included 14 cases of PIS. The patients’ clinical, pathological, and imaging features were retrospectively analyzed. Additionally, targeted DNA next-generation sequencing (NGS) was applied for the 481-gene panel to detect gene mutations. RESULTS: The average age for PIS patients was 31.4 years. Headache (7, 50.0%) was the most common symptom leading to the hospital visit. Twelve cases had PIS located in the supratentorial area and two in the cerebellopontine angle region. The maximum tumor diameter ranged from 19.0 mm to 130.0 mm, with an average diameter of 50.3 mm. Pathological types of tumors were heterogeneous, with chondrosarcoma being the most common, followed by fibrosarcoma. Eight of the 10 PIS cases that underwent MRI scanning showed gadolinium enhancement; 7 of these cases were heterogeneous, and 1 of them was garland-like. Targeted sequencing was performed in two cases and identified mutations in genes such as NRAS, PIK3CA, BAP1, KDR, BLM, PBRM1, TOP2A, DUSP2, and CNV deletions of SMARCB1. Additionally, the SH3BP5::RAF1 fusion gene was also detected. Of the 14 patients, 9 underwent a gross total resection (GTR), and 5 chose subtotal resection. Patients who underwent GTR displayed a trend toward superior survival. Among the 11 patients with available follow-up information, one had developed lung metastases, three had died, and eight were alive. CONCLUSION: PIS is extremely rare compared to extracranial soft sarcomas. The most common histological type of intracranial sarcoma (IS) is chondrosarcoma. Patients who underwent GTR of these lesions showed improved survival rates. Recent advancements in NGS aided in the identification of diagnostic and therapeutic PIS-relevant targets.
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spelling pubmed-102885192023-06-24 Primary intracranial sarcomas: a clinicopathological investigation Cai, Yu-Xiang Liu, Jin-Sheng Xu, Jian He, Yong-Ze Zhang, Huai-Nian Tian, Su-Fang Li, Zhi-Qiang Front Oncol Oncology BACKGROUND: The purpose of this study is to present a series of primary intracranial sarcomas (PIS), a rare type of tumor of the central nervous system, in order to improve our understanding of the disease. These tumors are heterogeneous and prone to recurrence after resection, exhibiting a high mortality rate. As PIS has yet to be understood and studied on a large scale, it is vital for further evaluation and research. METHODS: Our study included 14 cases of PIS. The patients’ clinical, pathological, and imaging features were retrospectively analyzed. Additionally, targeted DNA next-generation sequencing (NGS) was applied for the 481-gene panel to detect gene mutations. RESULTS: The average age for PIS patients was 31.4 years. Headache (7, 50.0%) was the most common symptom leading to the hospital visit. Twelve cases had PIS located in the supratentorial area and two in the cerebellopontine angle region. The maximum tumor diameter ranged from 19.0 mm to 130.0 mm, with an average diameter of 50.3 mm. Pathological types of tumors were heterogeneous, with chondrosarcoma being the most common, followed by fibrosarcoma. Eight of the 10 PIS cases that underwent MRI scanning showed gadolinium enhancement; 7 of these cases were heterogeneous, and 1 of them was garland-like. Targeted sequencing was performed in two cases and identified mutations in genes such as NRAS, PIK3CA, BAP1, KDR, BLM, PBRM1, TOP2A, DUSP2, and CNV deletions of SMARCB1. Additionally, the SH3BP5::RAF1 fusion gene was also detected. Of the 14 patients, 9 underwent a gross total resection (GTR), and 5 chose subtotal resection. Patients who underwent GTR displayed a trend toward superior survival. Among the 11 patients with available follow-up information, one had developed lung metastases, three had died, and eight were alive. CONCLUSION: PIS is extremely rare compared to extracranial soft sarcomas. The most common histological type of intracranial sarcoma (IS) is chondrosarcoma. Patients who underwent GTR of these lesions showed improved survival rates. Recent advancements in NGS aided in the identification of diagnostic and therapeutic PIS-relevant targets. Frontiers Media S.A. 2023-06-09 /pmc/articles/PMC10288519/ /pubmed/37361584 http://dx.doi.org/10.3389/fonc.2023.1195467 Text en Copyright © 2023 Cai, Liu, Xu, He, Zhang, Tian and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Cai, Yu-Xiang
Liu, Jin-Sheng
Xu, Jian
He, Yong-Ze
Zhang, Huai-Nian
Tian, Su-Fang
Li, Zhi-Qiang
Primary intracranial sarcomas: a clinicopathological investigation
title Primary intracranial sarcomas: a clinicopathological investigation
title_full Primary intracranial sarcomas: a clinicopathological investigation
title_fullStr Primary intracranial sarcomas: a clinicopathological investigation
title_full_unstemmed Primary intracranial sarcomas: a clinicopathological investigation
title_short Primary intracranial sarcomas: a clinicopathological investigation
title_sort primary intracranial sarcomas: a clinicopathological investigation
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288519/
https://www.ncbi.nlm.nih.gov/pubmed/37361584
http://dx.doi.org/10.3389/fonc.2023.1195467
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