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Updated: Feb 5, 2026

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Reporte de Caso de Paciente con Condrosarcoma Mixoide Extraskeletal

Kabhisha Gunasekaran^1,2, Vindya Johnston³, Daniel Wong^4,5

¹Acute Surgical Unit, Fiona Stanley Hospital, Murdoch, AUS.

|February 4, 2026

Abstract:

Extra-skeletal myxoid chondrosarcoma (EMC) is a type of rare sarcoma of uncertain differentiation. This malignancy is marked by the growth of primitive chondroid cells forming multiple nodules within a rich myxoid matrix. It is distinguished by a specific translocation resulting in the fusion gene EWSR1::NR4A3, which is a distinctive molecular hallmark of EMC. EMC is categorised as an intermediate-grade tumour and is distinguished by a prolonged clinical course with a high likelihood of local recurrence and distant metastasis. Surgical treatment is the only option for a cure for EMC, while non-surgical treatments are typically considered for recurrent or distant disease. This case report discusses an interesting case of a patient with EMC and further elaborates on the history, examination, imaging, pathological findings, and management of EMC.

Palabras clave:

agente antiangiogénico translocación cromosómica doble sitio extraskeletal condrosarcoma mixoide extraskeletal modalidades de imagen tumor de grado intermedio cirugía de malignidad radioterapia (rt)quimioterapia sistémica (stc)

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