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Monoclonal Blast Cell Proliferation in Transient Myeloproliferative Disorders

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Modern Trends in Human Leukemia IX

Part of the book series: Haematology and Blood Transfusion / Hämatologie und Bluttransfusion ((HAEMATOLOGY,volume 35))

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Abstract

Transient myeloproliferative disorder is a hematological condition observed during the neonatal period in patients with Down syndrome.[1] This disorder mimics congenital leukemia and the blast cells were often reported to show characteristics compatible with those of mega-karyoblasts [2] or pluripotent stem cells [3]. Although this disorder usually resolves gradually without antileukemic treatment, in some patients, leukemia develops after periods of spontaneous remission [4], raising questions about the benign origin of this disorder.

This work was supported by a Grant-in-Aid from the Ministry of Health and Welfare as part of a comprehensive 10-year Strategy for Cancer Control; by a Grant for Pediatric Research 63–06 from the Ministry of Health and Welfare; by a Grant-in-Aid for Cancer Research; and by the Japanese Foundation for Multidiciplinary Treatment of Cancer.

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© 1992 Springer-Verlag Berlin Heidelberg

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Miyashita, T., Mizutani, S., Asada, M., Fujimoto, J., Inaba, T., Furukawa, T. (1992). Monoclonal Blast Cell Proliferation in Transient Myeloproliferative Disorders. In: Neth, R., Frolova, E., Gallo, R.C., Greaves, M.F., Afanasiev, B.V., Elstner, E. (eds) Modern Trends in Human Leukemia IX. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 35. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76829-3_7

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  • DOI: https://doi.org/10.1007/978-3-642-76829-3_7

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-54360-2

  • Online ISBN: 978-3-642-76829-3

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