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Original Article

The Relationship between the Myelodysplastic Syndromes and the Myeloproliferative Disorders

Pages 443-449 | Received 14 Dec 1998, Published online: 01 Jul 2009

References

  • Verhoef G., Meeus P., Stul M., Mecucci C., Cassiman J. T., van den Berghe H., Boogaerts M. A. Cyto‐genetic and molecular studies of the Philadelphia transloca‐tion in myelodysplastic syndromes. Cancer Genetics and Cytogenetics 1992; 59: 161–166
  • Dash S., Rao N. R., Deodhar S. D., Varma N. Malignant mastocytosis and myelodysplastic syndrome. British Journal of Haematology 1991; 79: 530–531
  • Travis W. D., Li C. ‐Y., Yam L. T., Bergstralh E. J., Swee R. G. Significance of systemic mast cell disease with associated hematologic diagnosis. Cancer 1988; 62: 965–912
  • Beris P. Primacy clonal myelodysplastic syndrome. Seminars in Hematology 1989; 26: 216–233
  • Neuwirtováa R., Mocikováa K., Musilová J., Jelinek J., Havlíek R., Michalová K., Adamkov M. Mixed myelodysplastic and rnyeloproliferative syndromes. Leukemia Research 1996; 20: 711–126
  • Maschek H., Georgii A., Kaloutsi V., Werner M., Bande‐car K., Kressel M. ‐G., Choritz H., Freund M., Hufnagl D. Myelofibrosis in myelodysplastic syndromes: a retrospective study of 352 patients. European Journal of Haematology 1992; 48: 208–214
  • Lukowicz D. E., Myers T. J., Grasso J. A., Albala M. M. Sideroblastic anemia terminating in myelofibrosis. American Journal of Hematology 1982; 13: 253–251
  • Williams M. D., Shinton N. K., Finney R. D. Primary acquired sideroblastic anaemia and myeloprolifera‐tive disease: a report of three cases. Clinical and Laboratory Haematology 1985; 7: 113–118
  • Gupta R., Abdalla S. H., Bain B. J. Thrombocy‐tosis with sideroblastic erythropoiesis: a mixed myeloprolif‐erative/myelodysplastic syndrome. Leukemia & Lymphoma. 1998
  • Oscier D. G. Atypical chronic myeloid leukaemia. Is it a separate entity?. Leukemia Research 1994; 18(Suppl, 37)
  • Mufti G. J., Hamblin T. J., Seabright M. Acute transformation of a myeloproliferative state in sideroblastic anaemia with abnormal karyotype. Journal of Medical Genetics 1982; 19: 478
  • Craig A., Geary C. G., Love E. M., Liu‐Yin J. Red cell hypoplasia, thrombocytosis, and leucocytosis: myel‐odysplastic and proliferative syndrome. Journal of Clinical Pathology 1988; 41: 1168–1170
  • Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D. A. G., Gralnick H. R., Sultan C. Proposals for the classification of the myelodysplastic syndromes. British Journal of Haematology 1982; 51: 189–199
  • Bennett J. M., Catovsky D., Daniel M. T., Flandrin G., Galton D. A. G., Gralnick H. R., Sultan C., Cox C. The chronic myeloid Ieukaemias: guidelines for distinguishing granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals from the French‐American‐British Cooperative Leukaemia Group. British Journal of Haematology 1994; 87: 746–754
  • Germing U., Gatterman N., Minning H., Heyll A., Aul C. Problems in the classification of CMML‐dysplastic versus proliferative type. Leukemia Research 1997; 22: 871–878
  • Cervera J., Sanz G. F., Vallespi T., del Caflizo M. C., Irri‐guible R., Löpez F., Sahchez‐Morata C., Larrea L., Blanco A., Bentloch L., Juliá A., San Miguel J. F., Sanz M. A. Does WBC really define two different subtypes of chronic myelomonocytic leukemia (CMML)?. Leukemia Research 1997; 21(Suppl 1)S7
  • Oscier D., Chapman R. Commentary: the classification of chronic myelomonocytic leukaemia. Leukemia Research 1998; 22: 879–880
  • Matsushima T., Murukami H., Tsuchiya J. Myelodysplastic syndrome with bone marrow eosinophilia: clinical and cytogenetic features. Leukemia & Lymphoma 1994; 15: 491–497
  • Neri G., Daniel A., Hammond N. Chromosome 16q, eosinophilia, and leukemia. Cancer Genetics and Cytogenetics 1985; 14: 371–372
  • Kobayashi H., Kitano K., Shimodaira S., Ishida F., Saito H., Sonoyama M., Enokihara H., Furuta S. Eosinophilia in myelodysplastic syndrome with a (1221) (q23;q22) translocation. Cancer Genetics and Cytogenetics 1993; 68: 95–98
  • Inaba T., Shimazaki C., Inaba E., Hirata T., Ashihara E., Okhawa K., Oku N., Goto H., Murakami S., Fujita N., Misawa S., Nakagawa M. Inversion of chromosome 16 and eosinophilia in refractory anemia with ring sid‐eroblasts: report of a case. American Journal of Hematology 1993; 44: 134–138
  • Imai Y., Yasuhara S., Hanafusa N., Ohsaka A., Enokihara H., Tomizuka H., Sonoyama M., Miura Y., Tohda S., Nara N., Takahoshi A. Clonal involvement of eosino‐phils in therapy‐related myelodysplastic syndrome with eosinophilia, translocation t(1;7) and lung cancer. British Journal of Haematology 1996; 95: 710–714
  • Tinegate H. N., Chetty M. N. Basophilia as features of the myelodysplastic syndrome. Clinical and Laboratory Haematology 1986; 8: 269–271
  • El‐Rifai W., Pettersson T., Larramendy M. L., Knuutila S. Lineage involvement and karyotype in a patient with myelodysplasia and blood basophilia. European Journal of Haematology 1994; 53: 288–292
  • Solé R., Torrabedella M., Granada I., Florensa L., Vallespi T., Ribera J. M., Imguible D., Mella F., Woessner S. Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity. Leukemia Research 1993; 17: 717–720
  • Bain B. J. Eosinophilic leukaemias and the idiopathic hypereosinophilic syndrome. British Journal of Haematology 1996; 95: 2–9
  • Ross F. M., Hamilton M., Cook M. K., Irving J. B. A myelodysplastic syndrome with eosinophilia associated with a break in the short arm of chromosome 16. Leukemia 1987; 1: 680–681
  • Pearson M. G., Vardiman J. W., Le Beau M. M., Rowley J. D., Schwartz S., Kerman S. L., Cohen M. M., Fleischman E. W., Prigogina E. L. Increased numbers of marrow basophils may be associated with a t(6;9) in ANLL. American Journal of Hematology 1985; 18: 393–403
  • Keene P., Mendelow B., Pinto M. R., Bezwode W., Mac‐Dougall L., Falkson G., Ruff P., Bernstein R. Abnormalities of 12p13 and malignant proliferation of eosi‐nophils: a nonrandom association. British Journal of Haematology 1987; 67: 25–31
  • Ma S. K., Wong K. R., Chan J. K. C., Kwong Y. L. Refractory cytopenia with t(1;7), +8 abnormality and dysplastic eosinophils showing intranuclear Charcot‐Leyden crystals: a fluorescence in situ hybridization study. British Journal of Haematology 1995; 90: 216
  • Pérez‐Losada A., Woessner S., S61e F., Florensa L., Granena A. Refractory anaemia with hypereosino‐philia and clonal abnormal metaphases detected in the neu‐trophil granulopoietic series. Acta Haematologica 1994; 91: 80–83
  • Jani K., Kempski H. M., Reeves B. R. A case of myelodysplasia with eosinophilia having a translocation t(5;12)(q31;q13) restricted to myeloid cells but not involving eosinophils. British Journal of Haematology 1994; 87: 57–60
  • van den Berghe H., Vermaelen K., Mecucci C., Barbieri D., Tricot G. The 5q‐ anomaly. Cancer Genetics and Cytogenetics 1985; 17: 189–255
  • Jondeau K., Bouscary D., Viguié F., Picard R., Melle J., Lopez I., Fontenay‐Roupie M., Dreyfus R. Thrombocytemia (sic) and abnormal megakaryopoiesis associated with abnormality of chromosome lp34 in myelodysplastic syndromes. Leukemia 1996; 10: 1692–1695
  • Cuneo A., Tomasi P., Ferrari L., Balboni M., Piva N., Fagioli R., Castoldi G. Cytogenetic analysis of different cellular populations in chronic myelomonocytic leukemia. Cancer Genetics and Cytogenetics 1989; 37: 29–37
  • Dewald G. W., Davis M. P., Pierre R. V., O'Fallon J. R., Hoagland H. C. Clinical characteristics and prognosis of 50 patients with a myeloproliferative syndrome and deletion of part of the long arm of chromosome 5. Blood 1985; 66: 189–197
  • Koike T., Uesugi Y., Toba K., Narita M., Fuse I., Taka‐hashi M., Shibata A. 5q‐ syndrome presenting as essential thrombocythemia: myelodysplastic syndrome or chronic myeloproliferative disorders?. Leukemia 1995; 9: 517–518
  • Norrby A., Ridell B., Swolin B., Westin J. Rearrangement of chromosome No. 3 in a case of preleukemia with thrombocytosis. Cancer Genetics and Cytogenetics 1982; 5: 257–263
  • Carroll A. J., Poon M. ‐C., Robinson C., Crist W. M. Sideroblastic anaemia associated with thrombocytosis and a chromosome 3 abnormality. Cancer Genetics and Cytogenetics 1986; 22: 183–187
  • Secker‐Walker L., Mehta A., Bain B. on behalf of the UKCCG Abnormalities of 3q21 and 3q26 in myeloid malignancy: a United Kingdom Cancer Cytogenetic Group Study. British Journal of Haematology 1995; 91: 490–502
  • Parlier V., Tiainen M., Beris Ph., Miescher P. A., Knuutila S., Bellomo Jotterand M. Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosome in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria. British Journal of Haematology 1992; 81: 286–264
  • Longo L., Bessler M., Beris P., Swirsky D., Luzzatto L. Myelodysplasia in a patient with pre‐existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating within another clonal disease. British Journal of Haematology 1994; 87: 401–403
  • van Kamp H., Smit J. W., van den Berg E., Halie M. R., Vellenga E. Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. British Journal of Haematology 1994; 87: 399–400

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