Unusual blasts with basophilic granules in 2 cases of de novo acute myeloid leukemia with inv3(q21q26.2) and monosomy 7 and coexpression of CD2 and CD31

被引:2
作者
Treaba, Diana O. [1 ]
Chaump, Michael [1 ]
Merriam, Priscilla [2 ]
Ferreira, Karen [3 ]
Souza, Lydia [3 ]
Winer, Eric S. [2 ]
Barker, Barbara E. [3 ]
机构
[1] Brown Univ, Warren Alpert Med Sch, Rhode Isl Hosp, Dept Pathol & Lab Med, Providence, RI 02903 USA
[2] Brown Univ, Warren Alpert Med Sch, Rhode Isl Hosp, Div Hematol Oncol, Providence, RI 02903 USA
[3] Rhode Isl Hosp, Dept Pathol & Lab Med, Flow Cytometry Lab, Providence, RI 02903 USA
关键词
Acute myeloid leukemia; Inv3(q21q26.2) and monosomy 7; CD2 and CD31 coexpression; CYTOGENETIC ABNORMALITIES; ADULT; EXPRESSION; CELLS; IDENTIFICATION; PATTERNS; SURVIVAL; THERAPY; PECAM-1; FLT3;
D O I
10.1016/j.anndiagpath.2013.06.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Acute myeloid leukemia with inv3(q21q26.2)/t(3,3)(q21;q26.2) is a subtype of acute myeloid leukemia associated with significant dysmyelopoiesis and a poor prognosis. In more than a half of the cases, there is also monosomy 7. We present 2 young male patients with de novo acute myeloid leukemia with inversion 3 and monosomy 7 who had significant morphologic and immunophenotypical similarities. Both patients had circulating subsets of blasts with unusual intracytoplasmic basophilic granules and prominent bone marrow dysmegakaryopoiesis. The leukemic myeloid blasts were negative for myeloperoxidase and had aberrant coexpression of CD2 and CD31. Despite their morphologic and immunophenotypical similarities, only 1 of the patients achieved remission and remained free of disease 24 months after bone marrow transplant. The younger patient, who had also increased hemoglobin F and an associated FLT3 D835 variant, had an acute myeloid leukemia refractory to chemotherapy and died 4 months after his diagnosis. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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