Trisomy of group C in a myeloproliferative disorder. Report of case.

نویسندگان

  • A Winkelstein
  • R S Sparkes
  • C G Craddock
چکیده

By ALAN WINKELSTEIN, ROBERT S. SPARKES AND CHARLES G. CRADDOCK I HE MYELOPROLIFERATIVE syndrome comprises a spectrum of neoplastic disorders with merging clinical, pathologic and hematologic features. These disorders result from the abnormal proliferation, either in the bone marrow or potential marrow sites, of one or more of the marrow elements. Morphologically, the syndrome can be subdivided into at least 6 entities: polycythemia vera, chronic granulocytic leukemia, myelofibrosis with myeloid Inetaplasia, thrombocytothemia, acute granulocytic leukemia and DiGugliel11105 syndrome. Each of these conditions has its own distinguishing features, but atypical cases representing transitional forms or actual transformation from one entity to another are frequently encountered.1 Cytogenetic studies of the typical forms of the chronic myeloproliferative

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عنوان ژورنال:
  • Blood

دوره 27 5  شماره 

صفحات  -

تاریخ انتشار 1966