Trisomy 1q in a patient with severe aplastic anemia

  • Angelidis P.; 
  • Kojouri K.; 
  • Lee J.; 
  • Kern W.; 
  • Mulvihill J.J.; 
  • 외 1명
Citations

SCOPUS

9

초록

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. © 2006 Elsevier Inc. All rights reserved.

키워드

adult; aplastic anemia; article; bone marrow biopsy; case report; chromosome 1; chromosome analysis; chromosome breakage; chromosome translocation; clinical feature; disease course; disease severity; erythrocyte transfusion; human; laboratory test; male; priority journal; thrombocyte transfusion; treatment outcome; trisomy; trisomy 1q; Adult; Anemia, Aplastic; Chromosomes, Human, Pair 1; Female; Humans; Karyotyping; Trisomy
제목
Trisomy 1q in a patient with severe aplastic anemia
저자
Angelidis P.; Kojouri K.; Lee J.; Kern W.; Mulvihill J.J.; Li S.
DOI
10.1016/j.cancergencyto.2006.03.014
발행일
2006
유형
Article
저널명
Cancer Genetics and Cytogenetics
권
169
호
1
페이지
73 ~ 75