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B-cell marker expression in acute myeloid leukemia with plasmacytoid dendritic cell differentiation (pDC-AML) without RUNX1 lesions: An underrecognized diagnostic pitfall.

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Virchows Archiv : an international journal of pathology 📖 저널 OA 33.9% 2023: 2/2 OA 2024: 1/5 OA 2025: 13/33 OA 2026: 25/75 OA 2023~2026 2026
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출처

George GV, Hegde NV, Fang H, Jelloul FZ, Medeiros LJ, Wang W, El Hussein S

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The co-expression of myeloid and B-cell antigens is characteristic of mixed-phenotype acute leukemia (MPAL)-B/myeloid.

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APA George GV, Hegde NV, et al. (2026). B-cell marker expression in acute myeloid leukemia with plasmacytoid dendritic cell differentiation (pDC-AML) without RUNX1 lesions: An underrecognized diagnostic pitfall.. Virchows Archiv : an international journal of pathology. https://doi.org/10.1007/s00428-026-04412-6
MLA George GV, et al.. "B-cell marker expression in acute myeloid leukemia with plasmacytoid dendritic cell differentiation (pDC-AML) without RUNX1 lesions: An underrecognized diagnostic pitfall.." Virchows Archiv : an international journal of pathology, 2026.
PMID 41582188 ↗

Abstract

The co-expression of myeloid and B-cell antigens is characteristic of mixed-phenotype acute leukemia (MPAL)-B/myeloid. This finding can also be observed in AML with t(8;21)(q22;q22)/RUNX1::RUNX1T1, as well as in cases of AML with other RUNX1 rearrangements, copy number gains, or mutations. AML with plasmacytoid dendritic cell (pDC) differentiation (pDC-AML) containing clonally-related myeloblasts and neoplastic pDCs, are enriched for RUNX1 mutations and have been shown to exhibit B-cell marker expression. Here, we present two cases of pDC-AML with B-cell marker expression in which RUNX1 aberrations were not identified. Although previously we speculated on the role of RUNX1 in the aberrant expression of B-cell markers such in cases, the absence of RUNX1 lesions in the current cases supports the potential inherent ability of pDCs to express B-cell markers during maturation.

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