Article

RARE CASE OF PRIMARY AML WITH TP53 DELETION

2025-08-01

Abstract excerpt

P53-mutated AML is typically therapy-related and rarely seen as primary disease, especially in children. We report a case of pediatric AML with P53 deletion. A 5-year-old male presented with fever for 2-week duration. Peripheral smear showed 6% atypical cells, and bone marrow aspirate revealed 30% blasts. Flow cytometry confirmed AML. Following induction therapy with cytarabine and daunomycin; the disease was pers...

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Literature Corpus work: 1713df57-5952-5f42-9c2f-429f4b5995d9
DOI: 10.22541/au.175404795.51667520/v1

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