Shanske A L, Kalman A, Grunwald H
Department of Pediatrics, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA.
Br J Haematol. 1996 Dec;95(3):524-6. doi: 10.1046/j.1365-2141.1996.d01-1928.x.
An association between eosinophilia and a structural chromosome abnormality has been noted in patients with acute non-lymphoblastic leukaemia (ANLL) and a deletion of the long arm of chromosome 16. There have been a number of other associations of specific chromosome abnormalities with neoplastic diseases involving the eosinophilic lineage; these include chromosome 12 short arm rearrangements, trisomy 8, t(8;21), t(5;14) and t(5;12). We report a patient with a myeloproliferative disorder characterized by chronic eosinophilic leukaemia complicated by autoimmune haemolytic anaemia and a previously unreported translocation (3;5)(p13;q13), and discuss the possible contribution of the RASA gene, localized to 5q13.3, to the development of the malignant phenotype.
在急性非淋巴细胞白血病(ANLL)且16号染色体长臂缺失的患者中,已注意到嗜酸性粒细胞增多与结构性染色体异常之间存在关联。特定染色体异常与涉及嗜酸性粒细胞谱系的肿瘤性疾病还有许多其他关联;这些包括12号染色体短臂重排、8三体、t(8;21)、t(5;14)和t(5;12)。我们报告了一名患有骨髓增殖性疾病的患者,其特征为慢性嗜酸性粒细胞白血病并发自身免疫性溶血性贫血以及一种先前未报道的易位(3;5)(p13;q13),并讨论了定位于5q13.3的RASA基因对恶性表型发展的可能作用。