Molecular characterization of complex chromosomal rearrangement: First report of novel t(7;12) (q11;q22) as part of a complex karyotype in de novo AML-M2 case

被引:1
|
作者
Ahmad, Firoz [1 ]
Dalvi, Rupa [2 ]
Mandava, Swarna [2 ]
Das, Bibhu R. [1 ]
机构
[1] SRL Ltd, Res & Dev, Bombay 400062, Maharashtra, India
[2] SRL Ltd, Cytogenet Div, Bombay 400062, Maharashtra, India
关键词
Acute myeloid leukemia; Cytogenetics; Chromosomal microarrays; Novel t(7; 12); India; ACUTE MYELOID-LEUKEMIA; MONOSOMAL KARYOTYPE; PROGNOSIS; ABNORMALITIES;
D O I
10.1016/j.prp.2014.08.015
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The strong association of diagnostic karyotype with clinical outcome has made cytogenetics one of the most valuable diagnostic and prognostic tools for acute myeloid leukemia (AML) till today. Complex chromosomal findings are reported to be seen in nearly 10-15% of adult AMLs and are generally associated with poor outcome. In the current report, we present the results of hematologic, immunophenotypic, cytogenetic, chromosomal microarray and molecular analyses of a 60-year-old female patient diagnosed with AML-M2. Cytogenetic analysis revealed complex chromosomal findings involving seven different chromosomes. However, cytogenetic analyses were not able to precisely unveil all karyotypic changes, hence chromosomal microarray was used for further characterization. The most interesting observation was identification of a t(7;12) (q11;q22) as part of this complex karyotype. To the best of our knowledge, this is the first report of identification of novel t(7;12) (q11;q22) as part of a complex karyotype in de nova AML-M2. (C) 2014 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1090 / 1094
页数:5
相关论文
共 41 条
  • [21] A de novo Complex Chromosomal Rearrangement of 46,XX,t(7;15;13)(p15;q21;q31) in a Female with an Adverse Obstetric History
    Iyer, Priya A.
    Vyas, Jaya C.
    Ranjan, Prabhat
    saranath, Dhananjaya
    INTERNATIONAL JOURNAL OF HUMAN GENETICS, 2009, 9 (02) : 139 - 143
  • [22] C7orf2 gene is interrupted within intronic region by a de novo reciprocal chromosomal translocation t (5,7)(q11, q36) in a patient with preaxial polydactyly.
    Horikoshi, T
    Endo, N
    Shibata, M
    Suzuki, M
    Takahashi, E
    Shinka, T
    Nakahori, Y
    Ayusawa, D
    Nakabayashi, K
    Scherer, SW
    Noji, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 610 - 610
  • [23] A novel five-way translocation t(7;11;9;22;9)(q22;q13;q34;q11.2;q34) involving Ph chromosome in a patient of chronic myeloid leukemia: a case report
    Sho Yokota
    Yuichi Nakamura
    Masami Bessho
    Molecular Cytogenetics, 5
  • [24] A novel five-way translocation t(7;11;9;22;9)(q22;q13;q34;q11.2;q34) involving Ph chromosome in a patient of chronic myeloid leukemia: a case report
    Yokota, Sho
    Nakamura, Yuichi
    Bessho, Masami
    MOLECULAR CYTOGENETICS, 2012, 5
  • [25] Adult B lymphoblastic leukaemia/lymphoma with hypodiploidy (-9) and a novel chromosomal translocation t(7;12)(q22;p13) presenting with severe eosinophilia – case report and review of literature
    Farhat Abbas Bhatti
    Iftikhar Hussain
    Muhammad Zafar Ali
    Journal of Hematology & Oncology, 2
  • [26] Adult B lymphoblastic leukaemia/lymphoma with hypodiploidy (-9) and a novel chromosomal translocation t(7;12)(q22;p13) presenting with severe eosinophilia - case report and review of literature
    Bhatti, Farhat Abbas
    Hussain, Iftikhar
    Ali, Muhammad Zafar
    JOURNAL OF HEMATOLOGY & ONCOLOGY, 2009, 2 : 26
  • [27] ADULT B LYMPHOBLASTIC LEUKEMIA WITH A NOVEL DE NOVO CHROMOSOMAL TRANSLOCATION [der(9)t(9;12)(p24;q12),-12]: A CASE REPORT
    Gadhia, P. K.
    Shastri, G. D.
    Shastri, E. G.
    BALKAN JOURNAL OF MEDICAL GENETICS, 2014, 17 (01) : 69 - 71
  • [28] Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for cDNA
    Y Chinen
    T Taki
    K Nishida
    D Shimizu
    T Okuda
    N Yoshida
    C Kobayashi
    K Koike
    M Tsuchida
    Y Hayashi
    M Taniwaki
    Oncogene, 2008, 27 : 2249 - 2256
  • [29] Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for cDNA
    Chinen, Y.
    Taki, T.
    Nishida, K.
    Shimizu, D.
    Okuda, T.
    Yoshida, N.
    Kobayashi, C.
    Koike, K.
    Tsuchida, M.
    Hayashi, Y.
    Taniwaki, M.
    ONCOGENE, 2008, 27 (15) : 2249 - 2256
  • [30] MOLECULAR CYTOGENETIC ANALYSES OF 12P13.3 JARID1A GENE IN A CASE OF MYELODYSPALSTIC SYNDROME WITH A COMPLEX T(12;21)(P13;Q22)
    Buijs, A.
    Dekker, A. W.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 517 - 517