Glandular differentiation in dedifferentiated chondrosarcoma: molecular evidence of a rare phenomenon

Hum Pathol. 2015 Sep;46(9):1398-404. doi: 10.1016/j.humpath.2015.05.018. Epub 2015 Jun 5.

Abstract

Epithelial glandular differentiation in dedifferentiated chondrosarcoma has not been described. Our patient was a 64-year-old man with a history of prostate cancer status post-radiation and hormonal therapy. On screening bone scan, he was found to have increased uptake in his right femoral shaft. Biopsy revealed intermediate-grade conventional chondrosarcoma. Subsequent femoral resection was remarkable for an intermediate-grade chondrosarcomatous component juxtaposed to an area composed of anastomosing nests and cords of malignant epithelial cells showing nuclear atypia and increased mitotic activity. A fibroblastic-appearing spindle cell population was intimately associated with the epithelial cells. The epithelial cells labeled with 34bE12, AE1/AE3, EMA, and Vimentin (both spindled and epithelial components) while being negative for prostate-specific antigen, prostate specific acid phosphatase, cytokeratin 20, thyroid transcription factor-1, and CDX2. The patient developed local recurrence 9 months after the initial resection but has had no metastatic disease and consistently undetectable prostate-specific antigen levels. Deep parallel sequencing of the dedifferentiated component showed a nonsynonymous mutation at exon 4 of IDH1 gene at codon R132 leading to a substitution of arginine, with serine confirming glandular differentiation in dedifferentiated chondrosarcoma.

Keywords: Cytogenomic microarray; Dedifferentiated chondrosarcoma; Epithelial glandular differentiation; Mesenchymal epithelial transition; Metastasis; Next generation sequencing.

Publication types

  • Case Reports

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Biopsy
  • Cell Dedifferentiation*
  • Chondrosarcoma / enzymology
  • Chondrosarcoma / genetics*
  • Chondrosarcoma / pathology*
  • Chondrosarcoma / surgery
  • DNA Mutational Analysis
  • Exons
  • Femoral Neoplasms / enzymology
  • Femoral Neoplasms / genetics*
  • Femoral Neoplasms / pathology*
  • Femoral Neoplasms / surgery
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Immunohistochemistry
  • Isocitrate Dehydrogenase / genetics*
  • Male
  • Middle Aged
  • Mutation
  • Neoplasm Recurrence, Local
  • Osteotomy
  • Time Factors
  • Treatment Outcome

Substances

  • Biomarkers, Tumor
  • Isocitrate Dehydrogenase
  • IDH1 protein, human