[Clinicopathological and molecular characteristics of extraskeletal myxoid chondrosarcoma: an analysis of sixteen cases].

PubMed 2026

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Authors: X F Qin, L Li, R F Dong, K K Pan, M Zhang, L Zhao, T W Zhang, Y Ding
DOI: 10.3760/cma.j.cn112151-20251129-00787
Cited by: 0

Abstract

EMC is a rare mesenchymal malignancy that arises not only in soft tissues but also in bone. The predominant histological subtype is classical EMC, with a minority presenting as cell-rich EMC. FISH detection of NR4A3 gene rearrangements provides a crucial value for the diagnosis. It needs to be differentiated from myoepithelial tumors, chordomas and myxoid liposarcomas.

Fields of Study & Subjects

Sarcoma Diagnosis and Treatment Bone Tumor Diagnosis and Treatments Cardiac tumors and thrombi

Publication details

Journal / source
PubMed
Volume
55
Issue
2
Pages
160–166
Publication date
8 February 2026
Language
ZH