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Article

A Rare Case of Acute Promyelocytic Leukemia with ider(17)(q10)t(15;17)(q22;q21) and FLT3-ITD Mutation.

Clinical laboratory - 1 Feb 2026

Lee Jong Ho

Abstract excerpt

BACKGROUND: Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia characterized by the t(15;17)(q22;q21) translocation. Although it typically responds well to therapy, certain genetic aberrations, including ider(17)(q10)t(15;17)(q22;q21) and FLT3-ITD mutations, have unclear prognostic implications. METHODS: A 61-year-old female patient presented with dizziness and persistent bruising....

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Share to Chromosomes, Human, Pair 15
Share to Chromosomes, Human, Pair 17
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to fms-Like Tyrosine Kinase 3

Share to In Situ Hybridization, Fluorescence

Share to Leukemia, Promyelocytic, Acute

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Source

Identifiers

PMID: 41670515
DOI: 10.7754/Clin.Lab.2025.250537

Genes

FLT3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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