Myeloid neoplasm with t(3;8)(q26;q24): report of six cases and review of the literature

被引:6
作者
Xu, Xiangdong [1 ]
Su, Mu [2 ]
Levy, Norman B. [3 ]
Mohtashamian, Arash [4 ]
Monaghan, Sara [2 ]
Kaur, Prabhjot [3 ]
Zaremba, Charles [2 ]
Garcia, Rolando [2 ]
Broome, H. Elizabeth [5 ]
Dell'Aquila, Marie L. [5 ]
Wang, Huan-You [5 ]
机构
[1] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[3] Dartmouth Hitchcock Med Ctr, Dept Pathol, Lebanon, NH 03766 USA
[4] Naval Med Ctr, Dept Pathol, San Diego, CA USA
[5] Univ Calif San Diego Hlth Syst, Dept Pathol, San Diego, CA 92093 USA
关键词
Acute myeloid leukemia; myeloid dysplastic syndrome; t(3; 8)(q26; q24); EVI1; MDS1; SHWACHMAN-DIAMOND-SYNDROME; MYELODYSPLASTIC SYNDROME; EVI1; EXPRESSION; LEUKEMIA; ABNORMALITIES; 3Q26; DELETION; GENE;
D O I
10.3109/10428194.2013.878460
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Balanced translocation between chromosomes 3q26 and 8q24 is a very rare event. Here we report six patients with t(3;8)(q26;q24) either as a sole or as a part of genetic abnormalities. Five of the six patients were men with ages ranging from 41 to 84 years old. One patient had a long history of granulocyte colony stimulating factor (G-CSF) treatment. Three of the patients were initially diagnosed with acute myeloid leukemia, two with myelodysplastic syndrome and one with chronic myelogenous leukemia with blast crisis. The peripheral blood in all patients showed severe to moderate anemia; one had absolute neutropenia, one with neutrophilia; four had thrombocytopenia, two with thrombocytosis. The bone marrows from all patients showed dysmegakaryopoiesis with additional erythroid (three patients) and granulocytic (two patients) dysplasia. Cytogenetics revealed t(3;8)(q26;q24) as the sole abnormality in three patients. The majority of patients (4/6) had a poor clinical course, with an average survival of 10 months.
引用
收藏
页码:2532 / 2537
页数:6
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