Ossifying fibromyxoid tumor of soft partsreport of a case with novel cytogenetic findings

V. Sovani, G. V.N. Velagaleti, E. Filipowicz, Z. Gatalica, A. S. Knisely

Producción científica: Articlerevisión exhaustiva

37 Citas (Scopus)

Resumen

A slowly growing tumor of the left thenar region in a 40-year-old man had the classic features of an ossifying fibromyxoid tumor of soft parts, including an incomplete shell of lamellar bone; a center composed of nodular aggregates of small spindled, oval, and stellate cells in abundant myxoid stroma; and strong expression of vimentin, S-100, and neuron-specific enolase by the tumor cells. Clonal chromosomal abnormalities included loss of a chromosome 6, extra material of unknown origin attached to the long arm of chromosome 12, and an unbalanced translocation involving the short arm of a chromosome 6 and the long arm of a chromosome 14. The karyotype was interpreted as 45,XY, der(6;14)(p10;q10),add(12)(q24.3). The chromosomal abnormalities suggest osteochondroblastic rather than neuronal or schwannian lineage.

Idioma originalEnglish (US)
Páginas (desde-hasta)1-6
Número de páginas6
PublicaciónCancer Genetics and Cytogenetics
Volumen127
N.º1
DOI
EstadoPublished - may 2001
Publicado de forma externa

ASJC Scopus subject areas

  • Genetics
  • Molecular Biology
  • Cancer Research

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