Saitoh H, Komiyama A, Norose N, Morosawa H, Akabane T
Br J Haematol. 1981 May;48(1):79-84. doi: 10.1111/j.1365-2141.1981.00079.x.
Clinical studies were done on a patient with Chediak-Higashi syndrome (CHS) with special emphasis on the accelerated phase. In order to obtain further information on the accelerated phase, haematopoiesis was studied by bone marrow culture techniques. The patient was placed on ascorbic acid therapy but she entered the accelerated phase, although the therapy improved in vitro neutrophil function to some extent. Administration of microtubulytic drugs such as vincristine, vinblastine and colchicine was effective in the management of the accelerated phase. Numbers of macrophage-granulocytic (CFU-C) and erythroid (CFU-E) progenitor cells were markedly decreased or absent during the accelerated phase, being another indicator of the accelerated phase.
对一名患有切-希二氏综合征(CHS)的患者进行了临床研究,特别关注加速期。为了获取关于加速期的更多信息,采用骨髓培养技术对造血作用进行了研究。该患者接受了抗坏血酸治疗,尽管该治疗在一定程度上改善了体外中性粒细胞功能,但她仍进入了加速期。使用长春新碱、长春花碱和秋水仙碱等微管溶解药物对加速期的治疗有效。在加速期,巨噬细胞-粒细胞(CFU-C)和红系(CFU-E)祖细胞数量显著减少或缺失,这是加速期的另一个指标。