Literature DB >> 21156232

Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.

Gayoung Lim1, Min Jin Kim, Seung Hwan Oh, Sun Young Cho, Hee Joo Lee, Jin-Tae Suh, Juhie Lee, Woo-In Lee, Kyung Sam Cho, Tae Sung Park.   

Abstract

We present an unusual case study on acute myeloid leukemia associated with t(1;3) and extreme thrombocytosis, along with a thorough review on relevant literature of t(1;3) cases (58 patients). On the basis of this study and literature review, thrombocytosis (>400,000/μL) is a relatively common finding in one third of patients with t(1;3), whereas increase of platelet count by more than 1,000,000/μL is an extremely rare phenomenon, even among patients with t(1;3). To our knowledge, this study is the only documented case that recorded more than 2,000,000/μL of extreme thrombocytosis in a de novo acute myeloid leukemia patient with t(1;3) at initial diagnosis. Because only a few patients with t(1;3) responded to conventional chemotherapy, more aggressive therapy such as stem-cell transplantation should be considered to improve patient survival in t(1;3) cases.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21156232     DOI: 10.1016/j.cancergencyto.2010.08.001

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


  4 in total

1.  A novel case of extreme thrombocytosis in acute myeloid leukemia associated with isochromosome 17q and copy neutral loss of heterozygosity.

Authors:  Eunkyoung You; Sun Young Cho; John Jeongseok Yang; Hee Joo Lee; Woo-In Lee; Juhie Lee; Kyung Sam Cho; Eun Hae Cho; Tae Sung Park
Journal:  Ann Lab Med       Date:  2015-04-01       Impact factor: 3.464

2.  Acute mono-megakaryoblastic leukemia associated with extreme thrombocytosis and complex karyotype abnormalities.

Authors:  Rong Hu; Jia Li; Yanping Hu; Jihong Zhang; Miao Miao; Ke Zhu; Aijun Liao; Wei Yang; Zhuogang Liu
Journal:  Am J Case Rep       Date:  2013-05-17

3.  Detection of RUNX1-MECOM fusion gene and t(3;21) in a very elderly patient having acute myeloid leukemia with myelodysplasia-related changes.

Authors:  John Jeongseok Yang; Sun Young Cho; Jin-Tae Suh; Hee Joo Lee; Woo-In Lee; Hwi-Joong Yoon; Sun Kyung Baek; Tae Sung Park
Journal:  Ann Lab Med       Date:  2012-08-13       Impact factor: 3.464

Review 4.  Rare Cytogenetic Abnormalities and Alteration of microRNAs in Acute Myeloid Leukemia and Response to Therapy.

Authors:  Mohammad Shahjahani; Elahe Khodadi; Mohammad Seghatoleslami; Javad Mohammadi Asl; Neda Golchin; Zeynab Deris Zaieri; Najmaldin Saki
Journal:  Oncol Rev       Date:  2015-03-09
  4 in total

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