Dysplasia Has A Differential Diagnosis: Distinguishing Genuine Myelodysplastic Syndromes (MDS) From Mimics, Imitators, Copycats and Impostors

被引:65
作者
Steensma, David P. [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
关键词
Myelodysplastic syndromes (MDS); Differential diagnosis; Pathology; Dysplasia; Aplastic anemia; Nutritional deficiency; Copper deficiency; Sideroblastic anemia; Leukemia; Molecular diagnostics; WORLD-HEALTH-ORGANIZATION; IDIOPATHIC SIDEROBLASTIC ANEMIA; THERAPY-RELATED MYELODYSPLASIA; UNDETERMINED SIGNIFICANCE ICUS; ACUTE ERYTHROID LEUKEMIA; MARROW FAILURE SYNDROMES; ACUTE MYELOID-LEUKEMIA; BONE-MARROW; REFRACTORY-ANEMIA; APLASTIC-ANEMIA;
D O I
10.1007/s11899-012-0140-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Just as a pawnshop owner who is unable to distinguish a genuine Rolex (TM) watch from a cheap knockoff courts financial ruin, the physician who fails to discriminate between authentic myelodysplastic syndromes (MDS) and conditions resembling MDS risks misinforming or harming patients. This review summarizes minimal criteria for diagnosing MDS and discusses common diagnostic challenges. MDS needs to be separated from numerous neoplastic and non-clonal hematologic disorders that can mimic MDS, including other myeloid neoplasms, nutritional deficiencies, toxin exposures, aplastic anemia, and inherited disorders (e.g., congenital sideroblastic anemia). Some distinctions are more critical therapeutically than others; e.g., recognizing B12 deficiency is more important than parsing high-risk MDS from erythroleukemia. Diagnostically ambiguous cases may be assigned holding-pattern terms, "idiopathic cytopenia(s) of undetermined significance" (ICUS) or "idiopathic dysplasia of undetermined significance" (IDUS), while awaiting clarifying information or further clinical developments. In the future, advances in molecular pathology will improve diagnostic accuracy, especially in morphologically non-descript cases.
引用
收藏
页码:310 / 320
页数:11
相关论文
共 86 条
[1]   Clonal Evolution in Aplastic Anemia [J].
Afable, Manuel G., II ;
Tiu, Ramon V. ;
Maciejewski, Jaroslaw P. .
HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2011, :90-95
[2]   SNP array-based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes [J].
Afable, Manuel G., II ;
Wlodarski, Marcin ;
Makishima, Hideki ;
Shaik, Mohammed ;
Sekeres, Mikkael A. ;
Tiu, Ramon V. ;
Kalaycio, Matt ;
O'Keefe, Christine L. ;
Maciejewski, Jaroslaw P. .
BLOOD, 2011, 117 (25) :6876-6884
[3]   Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome [J].
Albers, Cornelis A. ;
Cvejic, Ana ;
Favier, Remi ;
Bouwmans, Evelien E. ;
Alessi, Marie-Christine ;
Bertone, Paul ;
Jordan, Gregory ;
Kettleborough, Ross N. W. ;
Kiddle, Graham ;
Kostadima, Myrto ;
Read, Randy J. ;
Sipos, Botond ;
Sivapalaratnam, Suthesh ;
Smethurst, Peter A. ;
Stephens, Jonathan ;
Voss, Katrin ;
Nurden, Alan ;
Rendon, Augusto ;
Nurden, Paquita ;
Ouwehand, Willem H. .
NATURE GENETICS, 2011, 43 (08) :735-737
[4]   The bone marrow aspirate of healthy subjects [J].
Bain, BJ .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 94 (01) :206-209
[5]  
Ballard HS, 1997, ALCOHOL HEALTH RES W, V21, P42
[6]  
Barrett J, 2000, SEMIN HEMATOL, V37, P15
[7]   G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia [J].
Beel, Karolien ;
Vandenberghe, Peter .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (10) :1449-1452
[8]   Clinical Effect of Point Mutations in Myelodysplastic Syndromes [J].
Bejar, Rafael ;
Stevenson, Kristen ;
Abdel-Wahab, Omar ;
Galili, Naomi ;
Nilsson, Bjoern ;
Garcia-Manero, Guillermo ;
Kantarjian, Hagop ;
Raza, Azra ;
Levine, Ross L. ;
Neuberg, Donna ;
Ebert, Benjamin L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2496-2506
[9]  
BENNETT JM, 1982, BRIT J HAEMATOL, V51, P189, DOI 10.1111/j.1365-2141.1982.tb08475.x
[10]   PROPOSALS FOR CLASSIFICATION OF ACUTE LEUKEMIAS [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1976, 33 (04) :451-&