Cytogenetic characterization of selected small round cell tumors of childhood

Cancer Genet Cytogenet. 1986 Apr 1;21(3):185-208. doi: 10.1016/0165-4608(86)90001-4.

Abstract

Small, round, blue-cell tumors (SRCT), including rhabdomyosarcoma, Ewing's sarcoma of bone and soft tissue, mesenchymal chondrosarcoma, small cell osteosarcoma, hemangiopericytoma, neuroblastoma, peripheral neurectodermal tumor (peripheral neuroepithelioma of bone and soft tissue), and the malignant small cell tumor of the thoracopulmonary region described by Askin (Askin's tumor), are often difficult to distinguish by light microscopy. We have evaluated the cytogenetics of these tumors by studying 24 tumor explants in short-term culture and 22 tumor cell lines. In Ewing's sarcoma (a tumor of unknown histogenesis), and in peripheral neuroepithelioma and Askin's tumor (tumors with evidence of neural origin), we have observed an indistinguishable t(11;22) translocation.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Bone Neoplasms / genetics*
  • Bone Neoplasms / pathology
  • Cell Line
  • Child
  • Child, Preschool
  • Chromosomes, Human, 21-22 and Y
  • Chromosomes, Human, 6-12 and X
  • Female
  • Ganglioneuroma / genetics
  • Ganglioneuroma / pathology
  • Humans
  • Karyotyping
  • Male
  • Neoplasm Metastasis
  • Neoplasms, Nerve Tissue / genetics*
  • Neoplasms, Nerve Tissue / pathology
  • Neuroectodermal Tumors, Primitive, Peripheral / genetics
  • Neuroectodermal Tumors, Primitive, Peripheral / pathology
  • Rhabdomyosarcoma / genetics
  • Rhabdomyosarcoma / pathology
  • Sarcoma, Ewing / genetics
  • Sarcoma, Ewing / pathology
  • Soft Tissue Neoplasms / genetics*
  • Soft Tissue Neoplasms / pathology
  • Translocation, Genetic*