Clonal evolution of monosomy 7 in acquired severe aplastic anemia: Two cases treated with allogeneic hematopoietic stem cell transplantation.

نویسندگان

  • Şule Mine Bakanay
  • Pervin Topçuoğlu
  • Aynur Uğur Bilgin
  • Kanay Yararbaş
  • Sibel Berker Karaüzüm
  • Muhit Özcan
  • Mutlu Arat
  • Levent Ündar
  • Osman Ilhan
چکیده

Aplastic anemia (AA) may evolve into clonal diseases like myelodysplastic syndrome (MDS) and acute myeloblastic leuke¬mia (AML). Monosomy 7 is a poor prognostic chromosomal abnormality commonly associated with therapy related MDS and secondary AML. It has also been associated with leukomogenic transformation in AA. We present here two adult ma¬le patients with acquired severe AA. Both patients had received immunosuppressive therapy (IST) as first line treatment and had monosomy 7 positive clone at transformation to MDS with refractory anemia and excess of blast (RAEB-II) and AML, respectively. Both patients have undergone allogeneic hematopoietic stem cell (HSC) transplantation from their HLA identical donors (unrelated and sibling).

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Monosomy 7 in donor cell-derived leukemia after bone marrow transplantation for severe aplastic anemia: Report of a new case and review of the literature

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عنوان ژورنال:
  • Turkish journal of haematology : official journal of Turkish Society of Haematology

دوره 25 2  شماره 

صفحات  -

تاریخ انتشار 2008