Korean J Lab Med.  2010 Dec;30(6):540-546. 10.3343/kjlm.2010.30.6.540.

Differential Blast Counts Obtained by Automated Blood Cell Analyzers

Affiliations
  • 1Department of Laboratory Medicine, The Catholic University of Korea College of Medicine, Seoul, Korea. hankja@catholic.ac.kr

Abstract

BACKGROUND
Automated blood cell analyzers often read leukemic blasts as normal cells. In this study, we evaluated the 5-part differential patterns of blasts using automated analyzers to determine if they can differentiate among blast types.
METHODS
Blood samples containing 10% or more blasts were collected from patients with acute leukemia (N=175). The 5-part differential count was conducted using DxH 800 (Beckman Coulter, USA) and XE-2100 analyzers (Sysmex Co., Japan), and the results were compared with manual differential counts, which was used as a reference method.
RESULTS
The DxH 800 reported the 5-part white blood cell differential count in 98.9% of the cases. The XE-2100 provided an invalid automated differential count in 72% of the cases. Both analyzers counted most lymphoblasts as lymphocytes and most myeloblasts as monocytes. In 11 cases, the DxH 800 reported a 5-part differential count without a blast flag.
CONCLUSIONS
Some automated analyzers are able to recognize and count blasts according to their characteristic cell types. Therefore, complete blood counts obtained automatically can provide valuable data for making provisional decisions regarding the lineage of leukemia cells before further investigation.

Keyword

Blast; Blood cell analyzer; Leukocyte differential; Manual differential

MeSH Terms

Acute Disease
Automation
Blood Cell Count/*instrumentation/methods
Humans
Leukemia/blood/*diagnosis
Leukemia, Monocytic, Acute/blood/diagnosis
Leukemia, Myeloid, Acute/blood/diagnosis
Leukemia, Promyelocytic, Acute/blood/diagnosis
Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood/diagnosis

Figure

  • Fig. 1. (A) A lymphoblast from an ALL case in which the blasts were counted as monocytes in the DxH 800; it showed irregularly shaped nuclei and cytoplasmic vacuoles. (B) A lymphoblast from a case of ALL in which the blasts were counted as lymphocytes in the DxH 800; it showed round nuclei with dispersed chromatin. (C) A lymphoblast from a case of T-ALL that did not generate blast flags; it showed coarse chromatin and abundant cytoplasm. All photomicrographs are ×1,000 magnification.


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