Cargando…

A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: case report and review of literature

The t (8; 21) (q22; q22) with the resulting RUNX1- RUNX1T1 rearrangement is one of the most common cytogenetic abnormalities in acute myeloid leukemia (AML). It is associated with favorable prognosis. The t (5; 17) (q35; q21) is an uncommon translocation, fuses the gene for the nucleophosmin (NPM) t...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zahra, Kmira, Cherif, Wided, Ahmed, Gereisha, Regaieg, Haifa, Nesrine, Ben Sayed, Zaier, Monia, Mootamri, Wided, Youssef, Yosra Ben, Brahem, Nejia, Sennana, Halima, Khelif, Abderrahim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Impact Journals LLC 2023
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328316/ https://www.ncbi.nlm.nih.gov/pubmed/37427149 http://dx.doi.org/10.18632/genesandcancer.232

Ejemplares similares

A challenging diagnosis of plasmablastic lymphoma: importance of integrating morpholgy immunohistochemistry and flow cytometry findings (case report)
por: Kmira, Zahra, et al.
Publicado: (2023)

A novel t(3;12)(q21;p13) translocation in a patient with accelerated chronic myeloid leukemia after imatinib and nilotinib therapy
por: Bennour, Ayda, et al.
Publicado: (2013)

PB2263: TOXICITY PROFILE OF SALVAGE CHEMOTHERAPY REGIMENS IN PATIENTS WITH RELAPSED/ REFRACTORY HODGKIN LYMPHOMA.
por: Zahra, Kmira, et al.
Publicado: (2023)

PB2262: PROGNOSTIC FACTORS IN PATIENTS WITH RELAPSED/REFRACTORY HODGKINN LYMPHOMA
por: Zahra, Kmira, et al.
Publicado: (2023)

PB2560: LYSOSOMAL STORAGE DISEASES: GUACHER’S DISEASE AND NIEMANPICK ‘S DISEASES: STUDY OF CLINICAL, CYTOLOGICAL AND ENZYMATIC ASPECTS
por: Mohamed, Lina, et al.
Publicado: (2023)

Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion
por: PANAGOPOULOS, IOANNIS, et al.
Publicado: (2013)

PB2556: MEGALOBLASTIC ANEMIA: EPIDEMIOLOGICAL, CLINICAL, AND ETIOLOGICAL PROFILE: ABOUT 200 CASES.
por: Zahra, Kmira, et al.
Publicado: (2023)

Systemic mastocytosis associated with t(8;21)(q22;q22) acute myeloid leukemia
por: Pullarkat, Sheeja T., et al.
Publicado: (2009)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

PB1739: ADVERSE EFFECTS OF ASPARAGINASE IN THE TREATMENT OF ACUTE LYMPHOBLASTIC LEUKEMIA
por: Chenbah, Wafa, et al.
Publicado: (2023)

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies
por: Su, Meng, et al.
Publicado: (2018)

Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
por: Ruiz-Botero, Felipe, et al.
Publicado: (2016)

PB1919: MATURE B-CELL NEOPLASMS CD5 NEGATIVE: CONFRONTATION CYTOMETRY-CYTOLOGY
por: Cheikh, Hanen Ben, et al.
Publicado: (2023)

Clinical case of acute myeloblastic leukemia with t(8;21)(q22;q22) in a patient with Klinefelter's syndrome
por: Slavcheva, Vanya, et al.
Publicado: (2010)

Functional characterization of BRCC3 mutations in acute myeloid leukemia with t(8;21)(q22;q22.1)
por: Meyer, Tatjana, et al.
Publicado: (2019)

伴继发性t（9;22）（q34;q11）的t（8;21）（q22;q22）急性髓系白血病一例报告及文献复习
Publicado: (2017)

Aggressive Clinicopathological Course of Myeloma with t(3;16) (q21;q22) Cytogenetic Abnormality
por: Bozkurt, Süreyya, et al.
Publicado: (2019)

伴t(3;21)(q26;q22)髓系肿瘤临床分析
Publicado: (2019)

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

Comparative analysis of a BAC contig of porcine chromosome 13q31-q32 and human chromosome 3q21-q22
por: Van Poucke, Mario, et al.
Publicado: (2005)

An unusual case of chronic lymphocytic leukemia with trisomy 12 presenting with prolymphocytic transformation and t(8;21)(q22;q22)
por: Bhushan, Mishi, et al.
Publicado: (2021)

PB1815: ADDITIONAL СYTOGENETIC ABNORMALITIES IN ADULT ACUTE MYELOID LEUKEMIA WITH T(8;21)(Q22;Q22)
por: Zotova, Olena, et al.
Publicado: (2023)

Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion
por: Tassano, Elisa, et al.
Publicado: (2015)

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation
por: Mishra, Divya, et al.
Publicado: (2014)

A Case of Acquired Aplastic Anemia after Severe Hepatitis- Probably Induced by the Pfizer/BioNTech Vaccine: A Case Report and Review of Literature
por: Kmira, Zahra, et al.
Publicado: (2023)

Association between Variants on Chromosome 4q25, 16q22 and 1q21 and Atrial Fibrillation in the Polish Population
por: Kiliszek, Marek, et al.
Publicado: (2011)

The 4q25, 1q21, and 16q22 polymorphisms and recurrence of atrial fibrillation after pulmonary vein isolation
por: Kiliszek, Marek, et al.
Publicado: (2016)

Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review
por: Ji, Jianling, et al.
Publicado: (2014)

Acute Myeloid Leukemia with t(8;21)(q22;q22) and Trisomy 4: A Rare Occurrence in a Female Child
por: Kamran, Shawana, et al.
Publicado: (2019)

Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas.
por: Forus, A., et al.
Publicado: (1998)

A rare case of acute promyelocytic leukemia with ider(17)(q10)t(15;17)(q22;q21) and favorable outcome
por: Liu, Yongming, et al.
Publicado: (2020)

6q21–22 deletion syndrome with interrupted aortic arch
por: Matsumoto, Ayumi, et al.
Publicado: (2015)

Cytogenetical and hematological analysis of chronic myelogenous leukemia patients with a novel case 52XX, t (1;9;22) (q23.3; q34; q11.2), +6, +8, i(9) (q10;q10), +18,+19,+21+der22 t(9;22)(q34;q11)
por: Asif, Muhammad, et al.
Publicado: (2022)

A New Three-Way Translocation t(4;11;7)(q21;q23;q22) in a Mixed-Phenotype Acute Leukemia
por: Takasaki, Hirotaka, et al.
Publicado: (2011)

A primary pediatric acute myelomonocytic leukemia with t(3;21)(q26;q22): A case report
por: Duan, Jia-xin, et al.
Publicado: (2023)

Analysis of 2 men with t(8;22)(q13;q13) and t(8;14)(q13;q22) chromosomal translocation karyotypes
por: Sun, Qijia, et al.
Publicado: (2022)

Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report
por: Wafa, Abdulsamad, et al.
Publicado: (2016)

A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization
por: Qi, Qingwei, et al.
Publicado: (2013)

A Novel KIT INDEL Mutation in Acute Myeloid Leukemia With t(8;21)(q22;q22); RUNX1-RUNX1T1
por: Lee, Jun Hyung, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_no5kq5rksbe4ufqcuo4ji1r9pp