Arora R S
Department of Pediatrics, Moolchand Khairatiram Hospital, New Delhi, India.
Indian Pediatr. 2009 Jun;46(6):525-7.
We report a case of chronic eosinophilic leukemia in a 9 year old girl who presented with anemia, thrombocytopenia, leucocytosis (mostly dysplastic eosinophils), lymphadenopathy and hepatosplenomegaly. There was no increase in blasts but myelofibrosis was seen in the bone marrow. A previously unreported translocation 46,XX,t(1;4)(q24;q35), was found on cytogenetic analysis and involvement of the myocardium was also present. Shortly after commencing steroids, the family abandoned therapy.
我们报告了一例9岁女孩的慢性嗜酸性粒细胞白血病,该女孩表现为贫血、血小板减少、白细胞增多(主要是发育异常的嗜酸性粒细胞)、淋巴结病和肝脾肿大。原始细胞没有增加,但骨髓中可见骨髓纤维化。细胞遗传学分析发现了一种先前未报道的易位46,XX,t(1;4)(q24;q35),并且心肌也受累。在开始使用类固醇后不久,家属放弃了治疗。