Ontology highlight
ABSTRACT: Rationale
Some acute myeloid leukemia (AML) patients present with features mimicking the classical hypergranular subtype of acute promyelocytic leukemia (APL) but without the typical promyelocytic leukemia/retinoic acid receptor α (PML/RARα) rearrangement. Herein, we report an AML patient resembling APL but with nucleoporin 98/retinoid acid receptor gamma gene (NUP98/RARG) fusion transcript and Runt-related transcription factor 1 (RUNX1) mutation.Patient concerns
An 18-year-old male presented at the hospital with a diagnosis of AML.Diagnoses
The patient was diagnosed with bone marrow examination. Bone marrow smear displayed 90.5% promyelocytes. Fluorescence in situ hybridization analysis failed to detect the PML/RARα fusion transcript or RARα amplification. While re
SUBMITTER: Wei W
PROVIDER: S-EPMC7535657 | biostudies-literature | 2020 Oct
REPOSITORIES: biostudies-literature