Abstract
The diagnosis of acute leukemia consists of morphological FAB classification, genetic abnormality assay, cytochemical analysis, and immunophenotype based on surface and cytoplasmic expression of antigens of blastic cells.1-6 The commonly used immunophenotypic classification of acute lymphoblastic leukemia (ALL) includes null ALL (only HLA-DR and/or CD19 antigens are present on blast surface), common ALL (HLA-DR, CD19, and CD10 expression on blasts), and pre-B subtype with cytoplasmic μ chain in CD10, HLA-DR, and CD19 positive cell.1,2,4,7 The heterogeneity of early B-cell differentiation antigens expression (atypical patterns) was described in a few cases, more often in null ALL subtype.3,5 It suggested that the earliest stages of B-cell development showed less stable antigen expression. The clinical meaning of this heterogeneity was unknown.6,8