Mixed phenotype acute leukemia, b/myeloid (bilineal and biphenotypic), with t (2; 22)(q35; q12); EWSR1-FEV
C Montgomery-Goecker, P Koduru… - Journal of Pediatric …, 2021 - journals.lww.com
Background: Ewing sarcoma breakpoint region 1 gene (EWSR1) rearrangements are
largely associated with the Ewing sarcoma family of tumors. Observations: We report the first …
largely associated with the Ewing sarcoma family of tumors. Observations: We report the first …
A complex karyotype, including a three-way translocation generating a NUP98-HOXD13 transcript, in an infant with acute myeloid leukemia
E Hidaka, M Tanaka, K Matsuda… - Cancer genetics and …, 2007 - Elsevier
We report the case of an infant with acute myeloblastic leukemia who had the abnormal
karyotype 46, XX, t (2; 11; 9)(q31; p15; q22), t (6; 11; 15)(q21; q23; q22), t (8; 10)(q13; q22) …
karyotype 46, XX, t (2; 11; 9)(q31; p15; q22), t (6; 11; 15)(q21; q23; q22), t (8; 10)(q13; q22) …
Pre-B acute lymphoblastic leukemia in a 3-year-old boy with pre-acute myelogenous leukemia myelodysplastic syndrome: cytogenetic evidence of common early …
HC Rossbach, MJ Sutcliffe, W Chamizo… - Journal of pediatric …, 1998 - journals.lww.com
Purpose: Myelodysplastic syndromes in children commonly evolve into acute leukemia,
usually acute myelogenous leukemia (AML) and rarely acute lymphoblastic leukemia (ALL) …
usually acute myelogenous leukemia (AML) and rarely acute lymphoblastic leukemia (ALL) …
A unique structural abnormality of chromosome 16 resulting in a CBFβ-MYH11 fusion transcript in a patient with acute myeloid leukemia, FAB M4
J O'Reilly, L Chipper, F Springall… - Cancer genetics and …, 2000 - Elsevier
A 43-year-old female with a peripheral white cell count of 118.0× 109/L and 96% blasts was
diagnosed with acute myeloid leukemia (AML), FAB M4. Cytogenetics, performed on a bone …
diagnosed with acute myeloid leukemia (AML), FAB M4. Cytogenetics, performed on a bone …
SEPTIN6 , a Human Homologue to Mouse Septin6, Is Fused to MLL in Infant Acute Myeloid Leukemia with Complex Chromosomal Abnormalities …
R Ono, T Taki, T Taketani, H Kawaguchi, M Taniwaki… - Cancer research, 2002 - AACR
Abstract t (X; 11) is a recurrent translocation in pediatric acute myeloid leukemia (AML). We
showed that the MLL gene on 11q23 was fused to the SEPTIN6 gene on Xq24, a human …
showed that the MLL gene on 11q23 was fused to the SEPTIN6 gene on Xq24, a human …
[引用][C] Identification of a novel MYH9 mutation in a patient with May‐Hegglin anomaly
K Otsubo, H Kanegane, K Nomura… - Pediatric Blood & …, 2006 - Wiley Online Library
To the Editor: May-Hegglin anomaly (MHA) is characterized by a triad of giant platelets,
thrombocytopenia, and Döhle body-like cytoplasmic inclusions in granulocytes [1]. In …
thrombocytopenia, and Döhle body-like cytoplasmic inclusions in granulocytes [1]. In …
Childhood myelodysplastic syndromes in a Brazilian population
LF Lopes, I Lorand-Metze - Pediatric hematology and oncology, 1999 - Taylor & Francis
Fourteen pediatric cases of myelodysplastic syndrome according to French-American-British
Cooperative Group (FAB) criteria were identified in a retrospective review of all cases of …
Cooperative Group (FAB) criteria were identified in a retrospective review of all cases of …
[PDF][PDF] Novel three‐way fusions among ZNF384, EWSR1 and EHMT1 genes in paediatric B cell precursor acute lymphoblastic leukaemia with translocations …
X Chen, F Wang, P Cao, Y Zhang, X Ma… - British Journal of …, 2019 - researchgate.net
ZNF384 fusions have recently been identified in B-cell precursor acute lymphoblastic
leukaemia (BCP-ALL), and nine partners have been reported (Lilljebjorn & Fioretos, 2017) …
leukaemia (BCP-ALL), and nine partners have been reported (Lilljebjorn & Fioretos, 2017) …
NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern
JDE de Rooij, IHIM Hollink, S Arentsen-Peters… - Leukemia, 2013 - nature.com
Cytogenetic abnormalities and early response to treatment are the main prognostic factors in
acute myeloid leukemia (AML). Recently, NUP98/NSD1 (t (5; 11)(q35; p15)), a …
acute myeloid leukemia (AML). Recently, NUP98/NSD1 (t (5; 11)(q35; p15)), a …
FISH identifies a KAT6A/CREBBP fusion caused by a cryptic insertional t (8; 16) in a case of spontaneously remitting congenital acute myeloid leukemia with a normal …
R Barrett, B Morash, D Roback… - Pediatric Blood & …, 2017 - Wiley Online Library
Cytogenetics can inform risk stratification in pediatric acute myeloid leukemia (AML). We
describe the first case of a newborn with leukemia cutis found to have AML harboring a …
describe the first case of a newborn with leukemia cutis found to have AML harboring a …