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

Gayoung Lim , 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
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引用次数: 9

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.

急性髓性白血病与t(1;3)(p36;q21)和极端血小板增多症相关:一项临床研究并文献回顾
我们提出了一个与t(1;3)和极端血小板增多症相关的急性髓性白血病的罕见病例研究,并对t(1;3)病例(58例)的相关文献进行了全面回顾。根据本研究和文献综述,血小板增多(40万/μL)在1 / 3的t患者中较为常见(1;3),而血小板计数增加超过100万/μL是极为罕见的现象,即使在t患者中也是如此(1;3)。据我们所知,本研究是唯一一个在初诊时记录超过2,000,000/μL的急性髓系白血病患者的极端血小板增多的病例。由于只有少数t(1;3)患者对常规化疗有反应,因此应考虑更积极的治疗,如干细胞移植,以提高t(1;3)患者的生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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