Acute megakaryoblastic leukemia associated with trisomy 21 demonstrates a distinct immunophenotype. Issue 4 (31st October 2014)

• Record Type: Journal Article
• Authors: Wang, Linlin; Peters, John M.; Fuda, Franklin; Li, Long; Karandikar, Nitin J.; Koduru, Prasad; Wang, Huan‐You; Chen, Weina
• Is Part Of: Cytometry. Volume 88:Issue 4(2015)
• Page Start: 244
• Page End: 252
• Publication Date: 2014-10-31
• Subjects: Flow cytometry -- Diagnostic use -- Periodicals; Cytodiagnosis -- Periodicals; 616.07582
• DOI: 10.1002/cyto.b.21198
• Languages: English
• ISSNs: 1552-4949

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cytob21198-sec-0001" sec-type="section"> <title>Background</title> <p>Acute megakaryoblastic leukemia (AMKL) is a rare form of acute myeloid leukemia that encompasses three distinct subgroups: children with Down syndrome (DS‐AMKL), children without DS (non‐DS‐AMKL), and adults (adult‐AMKL). We hypothesize that the biological differences in the subtypes of AMKL may be reflected in distinct immunophenotypic (IP) features. Our aims were to employ mutiparameter flow cytometry to establish a comprehensive IP spectrum of AMKL in multiple demographic groups and to determine whether the subtypes of AMKL demonstrate distinct immunophenotypes.</p> </sec> <sec id="cytob21198-sec-0002" sec-type="section"> <title>Methods</title> <p>Thirty‐seven AMKL cases were retrieved and subdivided into these three groups. Multiparameter flow cytometry was used to determine and compare the immunophenotypes. Available clinical, cytogenetic, and morphologic data were reviewed to confirm diagnoses.</p> </sec> <sec id="cytob21198-sec-0003" sec-type="section"> <title>Results</title> <p>While there is commonality in the expression pattern for a wide range of myelomonocytic markers in these three subtypes of AMKL, blasts in DS‐AMKL were more likely to express CD7 and CD11b than those in non‐DS‐AMKL and adult‐AMKL. Furthermore, blasts in DS‐AMKL were more likely to express CD13, CD33, and CD36 than non‐DS pediatric AMKL, and showed greater CD56 expression compared with adult AMKL.</p> </sec> <sec id="cytob21198-sec-0004" sec-type="section"> <title>Conclusions</title> <p>These results indicate that DS‐AMKL is related to but immunophenotypically distinct from non‐DS‐AMKL and adult‐AMKL. This distinct immunophenotypic pattern, co‐expression of CD7 and CD11b, has practical implications for characterization of AMKL. © 2014 International Clinical Cytometry Society</p> </sec> </abstract>