Molecular and clinicopathologic heterogeneity of intracranial tumors mimicking extraskeletal myxoid chondrosarcoma
Primary intracranial neoplasms with features of extraskeletal myxoid chondrosarcomas
(EMC) are extremely rare and poorly characterized tumors with only∼ 12 cases described …
(EMC) are extremely rare and poorly characterized tumors with only∼ 12 cases described …
[PDF][PDF] Intracranial extraskeletal myxoid chondrosarcoma: case report and literature review
JH Park, MJ Kim, CJ Kim… - Journal of Korean …, 2012 - synapse.koreamed.org
Intracranial extraskeletal myxoid chondrosarcoma is extremely rare, with only seven patients
previously reported. We present a case report of a 21-year-old woman admitted for …
previously reported. We present a case report of a 21-year-old woman admitted for …
Primary extraskeletal myxoid chondrosarcoma in cerebellum: a case report with literature review
Y Qin, H Zhang, CS Ke, J Huang, B Wu, C Wan… - Medicine, 2017 - journals.lww.com
Interventions: Emergent CT revealed an occupying lesion in the left cerebellum with
surrounding edema. A complete surgical excision of the lesion through a transcortical …
surrounding edema. A complete surgical excision of the lesion through a transcortical …
[HTML][HTML] Primary intracranial extraskeletal myxoid chondrosarcoma: A case report and review of literature
ZY Zhu, YB Wang, HY Li, XM Wu - World Journal of Clinical Cases, 2022 - ncbi.nlm.nih.gov
BACKGROUND Primary intracranial extraskeletal myxoid chondrosarcoma (EMC) is an
extremely rare low-to intermediate-grade malignant soft tissue sarcoma, and only 15 cases …
extremely rare low-to intermediate-grade malignant soft tissue sarcoma, and only 15 cases …
[HTML][HTML] Primary intracranial extra-skeletal myxoid chondrosarcoma of right lateral ventricle with EWSR1 gene fusion: a case report and review of literature
VK Selvaraj, DK Gudipudi, R Khera… - …, 2021 - ncbi.nlm.nih.gov
Background Primary intracranial malignancies with extra-skeletal myxoid chondrosarcoma
(EMC) features are extremely rare. EMC constitutes a distinct genomic entity characterised …
(EMC) features are extremely rare. EMC constitutes a distinct genomic entity characterised …
Chondrosarcoma of the tibial head during pregnancy: a challenging diagnosis
PP Roessler, J Schmitt, S Fuchs-Winkelmann… - Case …, 2014 - casereports.bmj.com
Chondrosarcoma is one of the most common malignant bone tumours in adults. However, it
rarely occurs during pregnancy. Therefore, reports on surgical and medical management of …
rarely occurs during pregnancy. Therefore, reports on surgical and medical management of …
Extraskeletal myxoid chondrosarcoma of the parotid gland
NB Fidele, W Tianfu, B Liu, Y Sun… - Annals of Maxillofacial …, 2019 - journals.lww.com
Extraskeletal myxoid chondrosarcoma (EMC) is a rare tumor with an estimated incidence of<
3% among of all soft-tissue sarcomas. It is characterized by a multinodular architecture …
3% among of all soft-tissue sarcomas. It is characterized by a multinodular architecture …
Primary Extraskeletal Falcine Myxoid Chondrosarcoma—A Case Report and Review of Literature
R Narayanan, RT Venugopal, SK KL… - Asian Journal of …, 2024 - thieme-connect.com
Intracranial chondrosarcomas are rare malignant lesions. Both skull base and dural-based
extraosseous chondrosarcomas have been reported to occur intracranially. Dural-based …
extraosseous chondrosarcomas have been reported to occur intracranially. Dural-based …
[HTML][HTML] Intracranial extraskeletal myxoid chondrosarcoma in fourth ventricle
YG Hong, J Yoo, SH Kim… - Brain Tumor Research …, 2021 - synapse.koreamed.org
We present an extremely rare case of intracranial extraskeletal myxoid chondrosarcoma. A
36-year-old male presented with dizziness persisting for 2 weeks. MRI of the patient showed …
36-year-old male presented with dizziness persisting for 2 weeks. MRI of the patient showed …
Extraskeletal myxoid chondrosarcoma of the nasopharynx
A Bhalla, V Osipov - Pathology-Journal of the RCPA, 2011 - journals.lww.com
Extraskeletal myxoid chondrosarcoma (EMCS) is a very rare sarcoma with malignant
chondroblast-like cells seen in a background of myxoid matrix. 1 Although the name implies …
chondroblast-like cells seen in a background of myxoid matrix. 1 Although the name implies …