Trisomy 1q in a patient with severe aplastic anemia

被引:8
|
作者
Angelidis, Prodromos
Kojouri, Kiarash
Lee, Jiyun
Kern, William
Mulvihill, John J.
Li, Shibo [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Oklahoma City, OK 73190 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73190 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK 73104 USA
关键词
D O I
10.1016/j.cancergencyto.2006.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aplastic anemia is a rare, serious disease characterized by hypocellular bone marrow and pancytopenia in the peripheral blood. Most cases are acquired, idiopathic, and without gross cytogenetic abnormalities. A few chromosome abnormalities have recurred among a small subset of patients, most commonly trisomy 8 and monosomy 7. Some of these chromosome abnormalities have prognostic and therapeutic significance, although for most the clinical relevance is not known. We present the case of a 40-year-old man with idiopathic severe aplastic anemia in bone marrow cells with trisomy of the whole long arm of chromosome 1 due to an unbalanced translocation between chromosomes 1 and 15 at breakpoints of q10 and 15q10. This clonal abnormality (which, to our knowledge, has not been previously reported in a patient with aplastic anemia) suggests that genes on 1q may be involved in marrow aplasia. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:73 / 75
页数:3
相关论文
共 50 条
  • [1] CASE OF PARTIAL TRISOMY 1Q
    KIMURA, S
    NARAHARA, K
    KODAMA, Y
    KIMOTO, H
    JAPANESE JOURNAL OF HUMAN GENETICS, 1979, 24 (03): : 159 - 160
  • [2] Severe aplastic anemia in a patient with severe hemophilia A
    Karadas, N.
    Zihni, C.
    Karapinar, D.
    Kavakli, K.
    Balkan, C.
    HAEMOPHILIA, 2012, 18 : 66 - 66
  • [3] PARTIAL TRISOMY 1Q IN 3 PATIENTS
    SANGER, R
    ALFI, O
    DONNELL, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 1974, 26 (06) : A75 - A75
  • [4] TRISOMY 1Q AS A TISSUE SPECIFIC MOSAIC
    KORNER, H
    SCHROCK, E
    SIEBKE, K
    GROSCHKE, U
    ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM, 1991, 46 (06): : 417 - 419
  • [5] Prenatal sonographic features of trisomy 1q
    Wax, Joseph R.
    Carpenter, Molly
    Chard, Renee
    Cartin, Angelina
    Pinette, Michael G.
    Blackstone, Jacquelyn
    JOURNAL OF CLINICAL ULTRASOUND, 2008, 36 (04) : 231 - 236
  • [6] PARTIAL TRISOMY 1Q IN IDIOPATHIC MYELOFIBROSIS
    DONTI, E
    TABILIO, A
    BOCCHINI, F
    FALZETTI, F
    MARTELLI, MF
    GRIGNANI, F
    DONTI, GV
    LEUKEMIA RESEARCH, 1990, 14 (11-12) : 1035 - &
  • [7] Triplication of 1q in Fanconi anemia
    Ferro, MT
    Vazquez-Mazariego, Y
    Ramiro, S
    Sanchez-Hombre, MC
    Villalon, C
    Garcia-Sagredo, JM
    Ulibarrena, C
    Sastre, JL
    San Roman, C
    CANCER GENETICS AND CYTOGENETICS, 2001, 127 (01) : 38 - 41
  • [8] Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia
    Oliveira, NISS
    Ribeiro, EMSF
    Raimondi, SC
    Bittencourt, MA
    Pasquini, R
    Cavalli, LJ
    LEUKEMIA RESEARCH, 2002, 26 (11) : 1047 - 1049
  • [9] First case of trisomy 13 plus mosaic trisomy 1q
    Liehr, T
    Schmidt, M
    Starke, H
    Ziegler, M
    Kittner, G
    Heller, A
    Rubtsov, N
    Trifonov, V
    Claussen, U
    FETAL DIAGNOSIS AND THERAPY, 2002, 17 (03) : 133 - 136
  • [10] A new patient with trisomy 1q(q42-qter): Evidence for a consistent phenotype.
    Morava, E
    Tsien, F
    Jackson, KE
    Marble, M
    JOURNAL OF INVESTIGATIVE MEDICINE, 1998, 46 (01) : 9A - 9A