Abstract

Acute promyelocytic leukemia (APL) is a unique and very deeply studied acute myeloid leukemia [...].

Highlights

  • Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

  • The typical molecular genetic feature of Acute promyelocytic leukemia (APL) is the rearrangement of RARA gene with PML and a few with other partner genes

  • There are still some rare cases lacking RARA fusion they share the same morphology and immunocytochemistry features with typical APL. The classification of such cases remains controversial. They are usually referred to as acute promyelocytic-like leukemias (APLL), and sometimes they were morphologically classified as M3 according to the FAB classification

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Summary

Not exhibited

Positive: CD13, CD33, CD117, CD56; negative: HLA-DR, CD34, CD38, CD15, CD14, CD7, CD2, CD3, CD4, CD8, CD19, CD20, CD10. ATRA+ATO, switched to IA, NR; HA, CR. Followed by 4 courses of HA and 1 course of EA as maintenance therapy [11]. Positive: MPO, CD13, CD33; partially positive: CD71, negative: CD14, CD19, CD34, CD38, CD64, CD117, CD11b, CD11c, HLA-DR

Cytogenetics and Molecular
Cytogenetics and Mutation
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