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

Key Points

• The research aims to highlight the clinical implications of acute promyelocytic leukemia with specific genetic mutations.
• Case report of a patient diagnosed with APL
• Analysis of genetic mutations, specifically ider(17) and FLT3-ITD
• Observation of treatment response and disease progression
• The patient exhibited an aggressive disease course
• Resistance to standard treatment was noted
• The findings indicate a need for intensified therapeutic strategies and closer monitoring