Abstract t (8; 16)(p11. 2; p13. 3)/KAT6A-CREBBP is a rare recurrent cytogenetic abnormality
associated with acute myeloid leukemia (AML). We report 15 cases with t (8; 16)(p11. 2; p13 …

Objectives CREBBP alterations are associated with many diseases including leukaemia.
However, CREBBP expression and its clinical relevance in paediatric acute lymphoblastic …

Objectives Acute myeloid leukemia (AML) with t (8; 16)(p11; p13) abnormalities is a rare,
aggressive, and diagnostically challenging subtype that results in KAT6A-CREBBP gene …

Objective: To describe the case of a child who presented hemophagocytic
lymphohistiocytosis (HLH) associated with acute monocytic leukemia after chemotherapy …

The translocation t (8; 16)(p11; p13), which results in fusion of the MOZ/MYST3/KAT6A gene
(8p11) and CBP/CREBBP gene (16p13), is characterized by unique morphologic and …

Erythrophagocytosis (EP) is extremely rare in de novo acute lymphoblastic leukemia (ALL).
We document a rare case, which in addition, showed extensive blast vacuolization. A …

Hemophagocytosis is a property of histiocytic lineage cells; it is rarely performed by
leukemic blasts. This phenomenon happens in approximately 1% of acute leukemias …

The acute myeloid leukemia secondary to polycythemia vera has a poor prognosis and
survival. We present an extremely rare case of polycythemia vera who developed an acute …

Case 0148 Acute myeloid leukemia with myelodysplasia-related changes and cryptic t(8;16)(p11;p13);
KAT6A/CREBBP Page 1 Case 0148 Acute myeloid leukemia with myelodysplasia-related …