Marshall G M, White L
Department of Paediatric Haematology and Oncology, Prince of Wales Childrens Hospital, Randwick, Sydney, Australia.
Am J Pediatr Hematol Oncol. 1989 Summer;11(2):178-83.
An 8-year-old boy with idiopathic hypereosinophilic syndrome (HES) is reported. He has been maintained in prolonged hematologic remission with vincristine and mercaptopurine despite an initial eosinophil count of 186 X 10(9)/L and a poor response to prednisone and hydroxyurea. Success with this combination of chemotherapeutic agents has not previously been reported in the management of HES. Progressive endomyocardial fibrosis required cardiac surgery 11 months after diagnosis. The management of this disorder is discussed with a review of the published literature.
报告了一名8岁特发性嗜酸性粒细胞增多综合征(HES)男孩。尽管初始嗜酸性粒细胞计数为186×10⁹/L,且对泼尼松和羟基脲反应不佳,但他通过长春新碱和巯嘌呤维持了长期血液学缓解。这种化疗药物组合在HES治疗中的成功此前未见报道。诊断后11个月,进行性心内膜纤维化需要心脏手术。结合已发表的文献对该疾病的治疗进行了讨论。