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CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review
BACKGROUND: Intracranial extraskeletal mesenchymal chondrosarcoma (EMCS) is a rare neoplasm and often misdiagnosed before histopathological examination due to its rarity. There were few reports previously on the radiological features of intracranial EMCS. We described a 20-year-old male patient with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552257/ https://www.ncbi.nlm.nih.gov/pubmed/36237268 http://dx.doi.org/10.21037/tcr-21-2547 |
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author | Chu, Jixiang Ma, Huan Wang, Yao Li, Kun Liao, Chengde Ding, Yingying |
author_facet | Chu, Jixiang Ma, Huan Wang, Yao Li, Kun Liao, Chengde Ding, Yingying |
author_sort | Chu, Jixiang |
collection | PubMed |
description | BACKGROUND: Intracranial extraskeletal mesenchymal chondrosarcoma (EMCS) is a rare neoplasm and often misdiagnosed before histopathological examination due to its rarity. There were few reports previously on the radiological features of intracranial EMCS. We described a 20-year-old male patient with intracranial EMCS focusing on the imaging characteristics. CASE DESCRIPTION: The patient was admitted to our hospital due to headache and dizziness for two months, without nausea, vomiting, limb convulsions and loss of consciousness during the illness. Pre-contrast computed tomography (CT) revealed a large slightly hyperdense mass with irregularly lobulated margins in the right parietal and occipital region and multiple patchy calcifications in peripheral of the lesion. The inner table of right parietal bone adjacent to the mass was compressed, thickened, and eroded. Magnetic resonance imaging (MRI) exhibited intermediate and hypo-intensity on T1-weighted images (T(1)WI) and slight hyper-intensity on T2-weighted images (T(2)WI) with extremely high intensity rim of cerebral spinal fluid (CSF) and low intensity flow-void vessel. The mass demonstrated heterogeneous remarkable enhancement and “dural tail” sign also was noted. The important imaging signs of this case are irregular calcifications of soft tissue on CT and “dural tail” sign on MRI. The patient underwent tumor resection and was followed up postoperatively with serial MRI every three months. He was alive without obvious clinical symptoms and evidence of recurrence for 9 months. EMCS is a highly invasive tumor and it is difficult to differentiate EMCS from the other intracranial malignant tumors only by clinical characteristics or findings of CT and conventional MR imaging. Radiotherapy and chemotherapy after radical resection are the best treatment choice. Therefore, postoperative patients should be reviewed routinely. CONCLUSIONS: A knowledge of the imaging features could facilitate differentiation of intracranial EMCS, but the final diagnosis depends on pathological examinations. This paper focuses on the imaging characteristics of EMCS and fully describes the details of lesions in order to provide clinicians with effective differential diagnosis information and improve clinical decision-making. |
format | Online Article Text |
id | pubmed-9552257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-95522572022-10-12 CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review Chu, Jixiang Ma, Huan Wang, Yao Li, Kun Liao, Chengde Ding, Yingying Transl Cancer Res Case Report BACKGROUND: Intracranial extraskeletal mesenchymal chondrosarcoma (EMCS) is a rare neoplasm and often misdiagnosed before histopathological examination due to its rarity. There were few reports previously on the radiological features of intracranial EMCS. We described a 20-year-old male patient with intracranial EMCS focusing on the imaging characteristics. CASE DESCRIPTION: The patient was admitted to our hospital due to headache and dizziness for two months, without nausea, vomiting, limb convulsions and loss of consciousness during the illness. Pre-contrast computed tomography (CT) revealed a large slightly hyperdense mass with irregularly lobulated margins in the right parietal and occipital region and multiple patchy calcifications in peripheral of the lesion. The inner table of right parietal bone adjacent to the mass was compressed, thickened, and eroded. Magnetic resonance imaging (MRI) exhibited intermediate and hypo-intensity on T1-weighted images (T(1)WI) and slight hyper-intensity on T2-weighted images (T(2)WI) with extremely high intensity rim of cerebral spinal fluid (CSF) and low intensity flow-void vessel. The mass demonstrated heterogeneous remarkable enhancement and “dural tail” sign also was noted. The important imaging signs of this case are irregular calcifications of soft tissue on CT and “dural tail” sign on MRI. The patient underwent tumor resection and was followed up postoperatively with serial MRI every three months. He was alive without obvious clinical symptoms and evidence of recurrence for 9 months. EMCS is a highly invasive tumor and it is difficult to differentiate EMCS from the other intracranial malignant tumors only by clinical characteristics or findings of CT and conventional MR imaging. Radiotherapy and chemotherapy after radical resection are the best treatment choice. Therefore, postoperative patients should be reviewed routinely. CONCLUSIONS: A knowledge of the imaging features could facilitate differentiation of intracranial EMCS, but the final diagnosis depends on pathological examinations. This paper focuses on the imaging characteristics of EMCS and fully describes the details of lesions in order to provide clinicians with effective differential diagnosis information and improve clinical decision-making. AME Publishing Company 2022-09 /pmc/articles/PMC9552257/ /pubmed/36237268 http://dx.doi.org/10.21037/tcr-21-2547 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Case Report Chu, Jixiang Ma, Huan Wang, Yao Li, Kun Liao, Chengde Ding, Yingying CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title | CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title_full | CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title_fullStr | CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title_full_unstemmed | CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title_short | CT and MRI findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
title_sort | ct and mri findings of intracranial extraskeletal mesenchymal chondrosarcoma—a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552257/ https://www.ncbi.nlm.nih.gov/pubmed/36237268 http://dx.doi.org/10.21037/tcr-21-2547 |
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