Myelodysplastic/Myeloproliferative Neoplasms

被引:39
作者
Cazzola, Mario [1 ]
Malcovati, Luca [1 ]
Invernizzi, Rosangela [2 ]
机构
[1] Univ Pavia, Sch Med, Dept Hematol Oncol, I-27100 Pavia, Italy
[2] Univ Pavia, Sch Med, Dept Internal Med, I-27100 Pavia, Italy
关键词
CHRONIC-MYELOMONOCYTIC-LEUKEMIA; ACQUIRED UNIPARENTAL DISOMY; MYELODYSPLASTIC SYNDROMES; RING SIDEROBLASTS; REFRACTORY-ANEMIA; PROGNOSTIC-FACTORS; TUMOR-SUPPRESSOR; C-CBL; MUTATIONS; TET2;
D O I
10.1182/asheducation-2011.1.264
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
According to the World Health Organization (WHO) classification of tumors of hematopoietic and lymphoid tissues, myelodysplastic/myeloproliferative neoplasms are clonal myeloid neoplasms that have some clinical, laboratory, or morphologic findings that support a diagnosis of myelodysplastic syndrome, and other findings that are more consistent with myeloproliferative neoplasms. These disorders include chronic myelomonocytic leukemia, atypical chronic myeloid leukemia (BCR-ABL1 negative), juvenile myelomonocytic leukemia, and myelodysplastic/myeloproliferative neoplasms, unclassifiable. The best characterized of these latter unclassifiable conditions is the provisional entity defined as refractory anemia with ring sideroblasts associated with marked thrombocytosis. This article focuses on myelodysplastic/myeloproliferative neoplasms of adulthood, with particular emphasis on chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts associated with marked thrombocytosis. Recent studies have partly clarified the molecular basis of these disorders, laying the groundwork for the development of molecular diagnostic and prognostic tools. It is hoped that these advances will soon translate into improved therapeutic approaches.
引用
收藏
页码:264 / 272
页数:9
相关论文
共 57 条
[1]   Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms [J].
Abdel-Wahab, O. ;
Pardanani, A. ;
Patel, J. ;
Wadleigh, M. ;
Lasho, T. ;
Heguy, A. ;
Beran, M. ;
Gilliland, D. G. ;
Levine, R. L. ;
Tefferi, A. .
LEUKEMIA, 2011, 25 (07) :1200-1202
[2]  
[Anonymous], 2008, WHO CLASSIFICATION T
[3]   Transcription intermediary factor 1γ is a tumor suppressor in mouse and human chronic myelomonocytic leukemia [J].
Aucagne, Romain ;
Droin, Nathalie ;
Paggetti, Jerome ;
Lagrange, Brice ;
Largeot, Anne ;
Hammann, Arlette ;
Bataille, Amandine ;
Martin, Laurent ;
Yan, Kai-Ping ;
Fenaux, Pierre ;
Losson, Regine ;
Solary, Eric ;
Bastie, Jean-Noel ;
Delva, Laurent .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) :2361-2370
[4]   Recent advances in diagnosis, molecular pathology and therapy of chronic myelomonocytic leukaemia [J].
Bacher, Ulrike ;
Haferlach, Torsten ;
Schnittger, Susanne ;
Kreipe, Hans ;
Kroeger, Nicolaus .
BRITISH JOURNAL OF HAEMATOLOGY, 2011, 153 (02) :149-167
[5]   The Role of the Iron Transporter ABCB7 in Refractory Anemia with Ring Sideroblasts [J].
Boultwood, Jacqueline ;
Pellagatti, Andrea ;
Nikpour, Maryam ;
Pushkaran, Beena ;
Fidler, Carrie ;
Cattan, Helen ;
Littlewood, Tim J. ;
Malcovati, Luca ;
Della Porta, Matteo G. ;
Jadersten, Martin ;
Killick, Sally ;
Giagounidis, Aristoteles ;
Bowen, David ;
Hellstrom-Lindberg, Eva ;
Cazzola, Mario ;
Wainscoat, James S. .
PLOS ONE, 2008, 3 (04)
[6]   The t(8;9)(p22;p24) translocation in atypical chronic myeloid leukaemia yields a new PCM1-JAK2 fusion gene [J].
Bousquet, M ;
Quelen, C ;
De Mas, V ;
Duchayne, E ;
Roquefeuil, B ;
Delsol, G ;
Laurent, G ;
Dastugue, N ;
Brousset, P .
ONCOGENE, 2005, 24 (48) :7248-7252
[7]  
Breccia M, 2006, HAEMATOLOGICA, V91, P1566
[8]   Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia [J].
Cazzola, M ;
Invernizzi, R ;
Bergamaschi, G ;
Levi, S ;
Corsi, B ;
Travaglino, E ;
Rolandi, V ;
Biasiotto, G ;
Drysdale, J ;
Arosio, P .
BLOOD, 2003, 101 (05) :1996-2000
[9]  
Cazzola M., 2005, Clinical Hematology, P721
[10]   Ring sideroblasts and sideroblastic anemias [J].
Cazzola, Mario ;
Invernizzi, Rosangela .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2011, 96 (06) :789-792