Literature DB >> 1756488

Trisomy 13: a preferentially male chromosome aberration interfering specifically with myeloid proliferation and differentiation? Report of a case and review of the literature.

B Pedersen1, I M Jensen.   

Abstract

A case of trisomy 13 is presented: a 73-year-old man with acute nonlymphocytic leukemia (ANLL), FAB borderline M1/M2, and peripheral leukocyte and platelet counts that were difficult to control with chemotherapy. A literature review shows that 35 cases of trisomy 13 are known at present. They are characterized by male predominance (76%), preferentially myeloid disorders (ANLL, myelodysplastic syndromes, chronic myeloid leukemia), leucocytosis, and relatively high platelet counts and hemoglobins. It is suggested that trisomy 13 is a specific nosologic entity with male predominance and characterized by interference with proliferation and differentiation in the myeloid differentiation series.

Entities:  

Mesh:

Year:  1991        PMID: 1756488     DOI: 10.1016/0165-4608(91)90192-w

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  1 in total

1.  Ring chromosome 8 and trisomy 8 in a patient with acute myeloid leukemia.

Authors:  Bibhas Kar; B Nandhini; R Revathi
Journal:  Indian J Hematol Blood Transfus       Date:  2009-04-06       Impact factor: 0.900

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.