Trisomy 15 as the sole abnormality in myelodysplastic syndromes: Case report and review of the literature

被引:4
|
作者
Morel, F [1 ]
Le Bris, MJ [1 ]
Herry, A [1 ]
Morice, P [1 ]
De Braekeleer, M [1 ]
机构
[1] CHU Morvan, Serv Cytogenet Cytol & Biol Reprod, Brest, France
关键词
trisomy; 15; Y chromosome loss; myelodysplastic disorder; chromosomal abnormality;
D O I
10.1080/1042819021000055084
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trisomy 15 as the sole autosomal anomaly is uncommon in hematological malignancies but could be preferentially associated with myelodysplasia. We report a 61-year-old man who developed pancytopenia following two courses of chemotherapy for chronic lymphoid leukemia. Cytogenetic studies at diagnosis of pancytopenia with R banding showed a 47,XY,+15[3]/45,X[3]/46,XY[14] karyotype. A review of the 53 cases of myelodysplastic syndromes (MDS) and myeloid related disorders associated with trisomy 15 reported in the literature showed that 18 of the 31 men also lost the Y chromosome in the trisomic 15 cell line. Their mean age was significantly higher than that of males who had not lost the Y chromosome ( p <0.05). The main feature of the patient reported here is the presence of two abnormal cell lines, one having lost the Y chromosome, the other having gained a chromosome 15. Therefore, the two events occurred independently, the loss of the Y chromosome being possibly due to aging and the trisomy 15 to the hematologic disorder.
引用
收藏
页码:549 / 551
页数:3
相关论文
共 50 条
  • [1] Behcet's disease associated with myelodysplastic syndromes - A case report and a review of the literature
    Ohno, E
    Ohtsuka, E
    Watanabe, K
    Kohno, T
    Takeoka, K
    Saburi, Y
    Kikuchi, H
    Nasu, M
    CANCER, 1997, 79 (02) : 262 - 268
  • [2] Trisomy 6 as the sole stemline abnormality in a patient with acute monocytic leukemia: a case report
    Manabe, Masahiro
    Asada, Reiko
    Hagiwara, Yuji
    Momose, Dai
    Sugano, Yasuyoshi
    Mazaki, Takeshi
    Koh, Ki-Ryang
    AMERICAN JOURNAL OF BLOOD RESEARCH, 2018, 8 (01): : 1 - 4
  • [3] Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid leukemia and myelodysplastic syndrome
    Wan, TSK
    Au, WY
    Chan, JCW
    Chan, LC
    Ma, SK
    LEUKEMIA RESEARCH, 1999, 23 (11) : 1079 - 1083
  • [4] Trisomy 5 as the sole abnormality in a case of acute lymphoblastic leukemia
    Sundareshan, TS
    Madhumathi, DS
    Appaji, L
    MEDICAL AND PEDIATRIC ONCOLOGY, 2003, 40 (03): : 188 - 190
  • [5] Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes
    Paulsson, K.
    Johansson, B.
    PATHOLOGIE BIOLOGIE, 2007, 55 (01): : 37 - 48
  • [6] TRISOMY 9 MOSAICISM SYNDROME - A CASE-REPORT AND REVIEW OF THE LITERATURE
    TARANI, L
    COLLORIDI, F
    RAGUSO, G
    RIZZUTI, A
    BRUNI, L
    TOZZI, MC
    PALERMO, D
    PANERO, A
    VIGNETTI, P
    ANNALES DE GENETIQUE, 1994, 37 (01): : 14 - 20
  • [7] Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism:: a case report and review of literature
    Redaelli, S
    Sala, E
    Roncaglia, N
    Colombo, C
    Crosti, F
    Villa, N
    Tagliabue, P
    Cappellini, A
    Dalprà, L
    PRENATAL DIAGNOSIS, 2005, 25 (02) : 140 - 147
  • [8] Epilepsy in trisomy 7 mosaicism: A case report and literature review
    Veerapandiyan, Aravindhan
    Gallentine, William B.
    Schoch, Kelly
    Shashi, Vandana
    JOURNAL OF PEDIATRIC NEUROLOGY, 2011, 9 (01) : 63 - 68
  • [10] Sevoflurane and bradycardia in infants with trisomy 21: A case report and review of the literature
    Walia, Hina
    Ruda, James
    Tobias, Joseph D.
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2016, 80 (01) : 5 - 7