Acute leukemias of ambiguous origin.

Am J Clin Pathol

Immunology Laboratory, University Hospital of Nancy-Brabois, Nancy, France.

Published: September 2015

AI Article Synopsis

  • This session focused on mixed-phenotype acute leukemia (MPAL) as part of a workshop dedicated to exploring acute leukemias with ambiguous origins.
  • Diagnostic criteria for major categories of MPAL, including B/myeloid, T/myeloid, B/T, and B/T/myeloid, were summarized, emphasizing the complexity of accurate diagnosis.
  • A comprehensive approach involving flow cytometry, immunohistochemical analysis, and awareness of diagnostic pitfalls is crucial, as misdiagnosis can occur with certain cases of B-acute lymphoblastic leukemia mimicking MPAL.

Article Abstract

Objectives: This session of the Society for Hematopathology/European Association for Haematopathology Workshop focused on acute leukemias of ambiguous origin.

Methods: We provide an overview of mixed-phenotype acute leukemia (MPAL) as recognized in the current World Health Organization classification and summarize diagnostic criteria for major categories of MPAL: B/myeloid, T/myeloid, B/T, and B/T/myeloid.

Results: Most MPAL cases submitted were B/myeloid and T/myeloid MPAL, the most frequent types, but three cases of B/T MPAL were also submitted, and examples of all categories are illustrated. We emphasize that a comprehensive approach to immunophenotyping is required to accurately establish the diagnosis of MPAL. Flow cytometry immunophenotyping using a large panel of antibodies is needed as well as confirmatory immunohistochemical analysis and cytochemistry studies for myeloperoxidase and nonspecific esterase. We discuss technical issues in determining blast lineage and possible pitfalls in MPAL diagnosis. In particular, rare cases of B-acute lymphoblastic leukemia (B-ALL) can express myeloperoxidase but are otherwise consistent with B-ALL and should be treated as such. Last, we review the differential diagnosis between acute undifferentiated leukemia and acute myeloid leukemia with minimal differentiation.

Conclusions: There was an agreement that diagnosis of MPAL can be challenging, especially if applied flow cytometry panels are not comprehensive enough.

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Source
http://dx.doi.org/10.1309/AJCPSTU55DRQEGTEDOI Listing

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