SQSTM1::RARA fusion in acute promyelocytic leukemia: the first case report and literature review

Key Points

• This report aims to describe the first identified case of SQSTM1::RARA fusion in acute promyelocytic leukemia and review relevant literature.
• Case report detailing the clinical presentation and laboratory findings of the patient.
• Literature review of existing cases and related genetic anomalies in acute promyelocytic leukemia.
• Identification of the SQSTM1::RARA fusion in a patient with acute promyelocytic leukemia.
• Review highlights the rarity and potential implications of this genetic fusion in leukemia diagnosis.