Chromosomal evolution and tumor progression in a myxoid liposarcoma

Authors

  • Charlotte Örndal
  • Nils Mandahl
  • Anders Rydholm
  • Mef Nilbert
  • Sverre Heim
  • Måns Åkerman
  • Felix Mitelman

DOI:

https://doi.org/10.3109/17453679009006497

Abstract

A myxoid liposarcoma showed macroscopic, histologic, and cytogenetic heterogeneity. In one of three myxoid nodules and in the surrounding lipoma-like tumor tissue, the translocation t(12;16)(g13;p11), known to be specific for myxoid liposarcoma, was found as the sole chromosomal abnormality. In the other two nodules, additional rearrangements involving chromosomes 1, 12, and 16 were found. These aberrations were probably secondary to the primary t(12;16), and are cytogenetic evidence of clonal evolution. The complex chromosome aberrations were present in those tumor parts that had more malignant histology, indicating that the acquisition of secondary chromosomal aberrations parallels the histologic manifestations of tumor progression.

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Published

1990-01-01

How to Cite

Örndal, C., Mandahl, N., Rydholm, A., Nilbert, M., Heim, S., Åkerman, M., & Mitelman, F. (1990). Chromosomal evolution and tumor progression in a myxoid liposarcoma. Acta Orthopaedica, 61(2), 99–105. https://doi.org/10.3109/17453679009006497