To the Editor: The inversion of chromosome 16, inv (16), a cytogenetic abnormality
expressed in core binding factor acute myeloid leukemias (AML), is associated with …

Abstract Abstract 5044 Translocation t (11; 17) is a rare chromosomal aberration that as an
isolated entity is not pathognomonic of any hematologic disorder. Within the wide spectrum …

Jumping translocations (JTs) are rare but recurrent cytogenetic abnormalities in
hematological malignancies and solid tumors [1]. Of the JTs reported in hematological …

Background: Acute myeloid leukemia (AML) is a heterogeneous group of malignant
neoplasm of hematopoietic disorders characterized by an abnormal proliferation of myeloid …

A 55-year-old man was admitted to our hospital because of worsening pancytopenia and
increasing blast cells in peripheral blood. The patient had a fourteen-year history of IgM …

Untitled Page 1 Page 2 Dicetak oleh (printed by) Airlangga University Press. (OC 019/01.15/AUP-C1E).
Kampus C Unair, Mulyorejo Surabaya 60115, Indonesia. Telp. (031) 5992246, 5992247 …

Background: Risk stratification is critical in the management of acute myeloid leukemia
(AML) and among the favorable subset translocations known, 8; 21 seems elusive in our …

A 54-year-old male presented with a history of generalized myalgia and low back pain for 6
weeks and one episode of epistaxis on the day of admission. Past medical history was …

We present a novel, rare but recurrent variant three way translocation of t (8; 21), t (8; 16;
21)(q22; q24; q22), as a primary cytogenetic abnormality, resulting in AML1/ETO fusion …