Parmley R T, Ogawa M, Darby C P, Spicer S S
Blood. 1975 Nov;46(5):723-34.
A child with congenital neutropenia was studied using bone marrow culture and ultrastructural and cytochemical techniques. The patient's marrow cells formed a large number of granulocytic colonies of normal size in culture, and her peripheral blood leukocytes produced adequate colony-stimulating factor. No serum inhibitors were identified. The patient's promyelocytes from direct marrow and culture appeared normal in ultrastructure, and primary granules, contained peroxidase and acid phosphatase activity. Myelocytes and rare segmented neutrophils from direct marrow specimens demonstrated atypical notched nuclei, myelin figures in Golgi lamellae and primary (azurophilic) granules, and no identifiable secondary (specific) granules. These data indicate an intrinsic neutrophil defect which allows normal proliferation of precursor cells, but results in abnormal granulogenesis and apparent inability to form secondary granules.
采用骨髓培养、超微结构和细胞化学技术对一名先天性中性粒细胞减少症患儿进行了研究。患者的骨髓细胞在培养中形成了大量大小正常的粒细胞集落,其外周血白细胞产生了足够的集落刺激因子。未发现血清抑制剂。直接取自骨髓和培养的患者早幼粒细胞超微结构正常,初级颗粒含有过氧化物酶和酸性磷酸酶活性。直接取自骨髓标本的中幼粒细胞和罕见的分叶核中性粒细胞显示出非典型的切迹核、高尔基体板层中的髓鞘样结构和初级(嗜天青)颗粒,且未发现可识别的次级(特异性)颗粒。这些数据表明存在一种内在的中性粒细胞缺陷,这种缺陷允许前体细胞正常增殖,但导致异常的粒细胞生成以及明显无法形成次级颗粒。