Acute Myeloid Leukemia with MECOM Rearrangement Presenting with Striking Hemophagocytosis
摘要
This first report described a 65-year-old female with AML with MECOM rearrangement, presenting with prominent hemophagocytosis. The case met WHO-HAEM5 diagnostic criteria despite < 20% blasts, highlighting both a novel clinical feature and the diagnostic challenge posed by differing classification systems.