Features of polycythemia vera in the 8p12 myeloproliferative syndrome

Jeanna L Welborn, Shelly Fenner, Robert Parks

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

The 8p12 myeloproliferative syndrome is a distinct myeloid disorder associated with a translocation involving chromosome region 8p12 (HUGO nomenclature). It is characterized by leukocytosis, eosinophilia, and a concurrent or rapid transformation to a T-cell lymphoblastic lymphoma. We report a case of polycythemia vera as a clinical presentation of the 8p12 myeloproliferative syndrome and review the literature. Atypical features in patients with polycythemia vera should be investigated with cytogenetic evaluation.

Original languageEnglish (US)
Pages (from-to)53-55
Number of pages3
JournalCancer Genetics and Cytogenetics
Volume199
Issue number1
DOIs
StatePublished - May 2010

ASJC Scopus subject areas

  • Cancer Research
  • Genetics
  • Molecular Biology

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