TRANSLOCATION T(11-22)(Q23-Q11) IN AN ADULT WITH ACUTE MONOBLASTIC LEUKEMIA

被引:0
|
作者
KOBAYASHI, H
MIYACHI, H
OGAWA, T
JIMBO, M
机构
关键词
CHIMERIC BCR-ABL MESSENGER RNA; DELETION-7Q; TRISOMY-8; MYELOMONOCYTIC PROGENITOR CELLS; LINEAGE SWITCH;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 66-year-old woman with acute monoblastic leukemia with t(11;22)(q23;q11), which was subsequently transformed into myeloblastic leukemia is reported. Such karyotype abnormality has not been reported in acute monoblastic leukemia. Cytogenetic analysis revealed 47,XX, +8, t(11;22)(q23;q11) in 19 out of 20 metaphases and 46, XX, del(7)(q22-q36), t(11;22)(q23;q11) in the remaining metaphase. Variant Ph1 was ruled out due to the absence of chimeric bcr-abl mRNAs. In remission cytogenetic findings showed normal karyotype. After 4 months, the patient relapsed with 20% myeloblasts replacing monoblasts in bone marrow. Cytogenetic analysis revealed 46, XX, del(7)(q22-q36), t(11;22)(q23;q11) in all metaphases. A possible explanation for this lineage switch may be the involvement of myelomonocytic progenitor cells.
引用
收藏
页码:527 / 532
页数:6
相关论文
共 50 条
  • [41] MLL-SEPT5 fusion transcript in infant acute myeloid leukemia with t(11;22)(q23;q11)
    Launay, Erika
    Henry, Catherine
    Meyer, Claus
    Chappe, Cline
    Taque, Sophie
    Boulland, Marie-Laure
    Ben Abdelali, Raouf
    Dugay, Frederic
    Marschalek, Rolf
    Bastard, Christian
    Fest, Thierry
    Gandemer, Virginie
    Belaud-Rotureau, Marc-Antoine
    LEUKEMIA & LYMPHOMA, 2014, 55 (03) : 662 - 667
  • [42] PROGRESS TOWARDS CLONING THE 22Q11 BREAKPOINT OF THE RECURRENT CONSTITUTIONAL T(11-22)
    BARNOSKI, BL
    EMANUEL, BS
    BELL, CJ
    STRAAKA, M
    TATSUMURA, Y
    BUDARF, ML
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 594 - 594
  • [43] MOLECULAR AND CYTOGENETIC STUDIES OF 22Q11 - THE 11Q22Q TRANSLOCATION
    EMANUEL, BS
    SYLVESTER, J
    ZACKAI, EH
    AMERICAN JOURNAL OF HUMAN GENETICS, 1983, 35 (06) : A130 - A130
  • [44] The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
    Tapia-Páez I.
    Kost-Alimova M.
    Hu P.
    Roe B.A.
    Blennow E.
    Fedorova L.
    Imreh S.
    Dumanski J.P.
    Human Genetics, 2001, 109 (2) : 167 - 177
  • [45] TRANSLOCATION (11-22) MAT INHERITED BY ONE DAUGHTER AS T (11-22) AND BY ANOTHER DAUGHTER AS T(11-15)
    TOMKINS, DJ
    KOCH, UM
    FREEMAN, CVP
    AMERICAN JOURNAL OF HUMAN GENETICS, 1980, 32 (06) : A90 - A90
  • [46] The recurrent t(11;22): FISH analysis of 11q23 and 22q11 in oogenesis.
    Emanuel, BS
    Conforto, D
    Cohen, MM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 216 - 216
  • [47] Acute leukemia with t(10;11)(p11-p15;q13-q23)
    Secco, C
    Wiernik, PH
    Bennett, JM
    Paietta, E
    CANCER GENETICS AND CYTOGENETICS, 1996, 86 (01) : 31 - 34
  • [48] The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
    Tapia-Páez, I
    Kost-Alimova, M
    Hu, P
    Roe, BA
    Blennow, E
    Fedorova, L
    Imreh, S
    Dumanski, JP
    HUMAN GENETICS, 2001, 109 (02) : 167 - 177
  • [50] The Constitutional Balanced Translocation t(11;22)(q23;q11.2)-An Indian Account
    Kamath, Vandana
    Srivastava, Vivi M.
    Yuvarani, S.
    Chacko, Mary Purna
    Bhattacharya, Saurabh Kumar
    Oommen, Samuel Phillip
    Danda, Sumita
    Korula, George
    JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2019, 13 (01) : GC1 - GC4