Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?

نویسندگان

  • Sílvia Saumell
  • Francesc Solé
  • Leonor Arenillas
  • Julia Montoro
  • David Valcárcel
  • Carme Pedro
  • Carmen Sanzo
  • Elisa Luño
  • Teresa Giménez
  • Montserrat Arnan
  • Helena Pomares
  • Raquel De Paz
  • Beatriz Arrizabalaga
  • Andrés Jerez
  • Ana B. Martínez
  • Judith Sánchez-Castro
  • Juan D. Rodríguez-Gambarte
  • José M. Raya
  • Eduardo Ríos
  • María Rodríguez-Rivera
  • Blanca Espinet
  • Lourdes Florensa
  • Ken Mills
چکیده

Isolated trisomy 8 is not considered presumptive evidence of myelodysplastic syndrome (MDS) in cases without minimal morphological criteria. One reason given is that trisomy 8 (+8) can be found as a constitutional mosaicism (cT8M). We tried to clarify the incidence of cT8M in myeloid neoplasms, specifically in MDS, and the diagnostic value of isolated +8 in MDS. Twenty-two MDS and 10 other myeloid neoplasms carrying +8 were studied. Trisomy 8 was determined in peripheral blood by conventional cytogenetics (CC) and on granulocytes, CD3+ lymphocytes and oral mucosa cells by fluorescence in situ hybridization (FISH). In peripheral blood CC, +8 was seen in 4/32 patients. By FISH, only one patient with chronic myelomonocytic leukemia showed +8 in all cell samples and was interpreted as a cT8M. In our series +8 was acquired in all MDS. Probably, once discarded cT8M by FISH from CD3+ lymphocytes and non-hematological cells, +8 should be considered with enough evidence to MDS.

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عنوان ژورنال:

دوره 10  شماره 

صفحات  -

تاریخ انتشار 2015