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Trisomy 1q in a patient with severe aplastic anemia
- Angelidis P.;
- Kojouri K.;
- Lee J.;
- Kern W.;
- Mulvihill J.J.;
- 외 1명
SCOPUS
9초록
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
- 제목
- Trisomy 1q in a patient with severe aplastic anemia
- 저자
- Angelidis P.; Kojouri K.; Lee J.; Kern W.; Mulvihill J.J.; Li S.
- 발행일
- 2006
- 유형
- Article
- 권
- 169
- 호
- 1
- 페이지
- 73 ~ 75
- 언어
- ENG
- 출판사
- Elsevier BV
- 발행국가
- 미국
- 분량
- 3 페이지
- ISSN
- P 0165-4608