Trisomy 1q in a patient with severe aplastic anemia

Prodromos Angelidis, Kiarash Kojouri, Jiyun Lee, William Kern, John J. Mulvihill, Shibo Li

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Aplastic anemia is a rare, serious disease characterized by hypocellular bone marrow and pancytopenia in the peripheral blood. Most cases are acquired, idiopathic, and without gross cytogenetic abnormalities. A few chromosome abnormalities have recurred among a small subset of patients, most commonly trisomy 8 and monosomy 7. Some of these chromosome abnormalities have prognostic and therapeutic significance, although for most the clinical relevance is not known. We present the case of a 40-year-old man with idiopathic severe aplastic anemia in bone marrow cells with trisomy of the whole long arm of chromosome 1 due to an unbalanced translocation between chromosomes 1 and 15 at breakpoints of q10 and 15q10. This clonal abnormality (which, to our knowledge, has not been previously reported in a patient with aplastic anemia) suggests that genes on 1q may be involved in marrow aplasia.

Original languageEnglish
Pages (from-to)73-75
Number of pages3
JournalCancer Genetics and Cytogenetics
Volume169
Issue number1
DOIs
Publication statusPublished - 2006 Aug
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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    Angelidis, P., Kojouri, K., Lee, J., Kern, W., Mulvihill, J. J., & Li, S. (2006). Trisomy 1q in a patient with severe aplastic anemia. Cancer Genetics and Cytogenetics, 169(1), 73-75. https://doi.org/10.1016/j.cancergencyto.2006.03.014