We describe herein a patient with acute promyelocytic leukemia (APL)-(ANLL-M3) whose
bone marrow cells in the second relapse showed t (1; 3)(p36; q21) together with t (15; …

The cytogenetic hallmark of acute promyelocytic leukemia (APL) is t (15; 17)(q22; q21)
involving the PML gene on chromosome 15q22 and the RARA gene on chromosome …

Key Clinical Message t (11; 17) is a rare but recognized finding usually found in Acute
Promyelocytic Leukemia with variant RARA translocation (APLv). We present a case of …

We report a woman with acute myeloid leukaemia (AML) type M2 according to FAB
classification, showing at (15; 17) apparently identical to that of acute promyelocytic …

Acute promyelocytic leukemia (APL) is a rare subtype of acute myeloid leukemia,
characterized by an accumulation of abnormal promyelocytes in the bone marrow, a severe …

Acute myeloid leukaemia (AML) with t (8; 21) is a common AML subtype and it is associated
with a favourable prognosis. Variants of this translocation, involving other chromosomes in …

The classification of acute myeloid leukemia (AML) recognizes a subgroup of diseases with
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …

The cellular and molecular genetic aberrations of hematopoietic and lymphoid tissues are
increasingly important in leukemia classification and are prognostically significant. Although …

Dear Editor, Acute promyelocytic leukemia (APL) represents 5–8% of acute myeloid
leukemias (AML), and is characterized by the classic t (15; 17)(q24. 1; q21. 2) translocation …

Acute promyelocytic leukemia (APL; M3 in the FAB classification) is specifically associated
with the t (15; 17)(q23; q12) and the consequent formation of a PML/RARA fusion gene. A …