MYELODYSPLASTIC-SYNDROME IN A CHILD WITH CONSTITUTIONAL TRISOMY-8 MOSAICISM AND NORMAL PHENOTYPE

被引:45
|
作者
HASLE, H
CLAUSEN, N
PEDERSEN, B
BENDIXHANSEN, K
机构
[1] DANISH CANC SOC,DEPT CYTOGENET,AARHUS,DENMARK
[2] AARHUS UNIV HOSP,DEPT PATHOL,DK-8000 AARHUS,DENMARK
关键词
D O I
10.1016/0165-4608(94)00099-W
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trisomy 8 is a frequently acquired cytogenetic abnormality in myeloid malignancies, but may also represent a constitutional chromosome abnormality with a wide phenotypic variation. We report a case of myelodysplastic syndrome (MDS) that developed in a child with trisomy 8 mosaicism and normal phenotype. Bone marrow (BM) cells all showed trisomy 8 with additional clonal abnormalities in most cells. Based on the present case and a review of previously published cases of myeloid malignancies in patients with trisomy 8 mosaicism, it appears likely that the malignant cells developed from the trisomic cell population, suggesting that constitutional trisomy 8 may be a predisposing condition to myeloid malignancies. Trisomy 8 in malignant cells is usually considered an acquired abnormality, but this implies a risk of ignoring a constitutional trisomy 8 mosaicism. Examination for constitutional trisomy 8, despite a normal phenotype, may therefore be warranted in hematologic malignancies with trisomy 8 of BM cells to evaluate further the possible association and to preclude erroneous use of trisomy 8 as a tumor marker.
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收藏
页码:79 / 81
页数:3
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