White J G
Am J Pathol. 1979 May;95(2):445-62.
The gray platelet syndrome (GPS) is a rare inherited disorder in which peripheral blood platelets are relatively large, vacuolated, and almost devoid of cytoplasmic granulation. In the present study we have evaluated the ultrastructure and cytochemistry of platelets from 2 patients with the GPS to determine precisely which organelles are missing from their cells. The findings indicate that gray platelets contain normal numbers of mitochondria, dense bodies, peroxisomes, and lysosomes but specifically lack alpha-granules. Preliminary studies of megakaryocytes from 1 of the 2 patients suggest that the defect in granule formation may lie at the level of the Golgi zone.
灰色血小板综合征(GPS)是一种罕见的遗传性疾病,其外周血血小板相对较大,呈空泡状,几乎没有细胞质颗粒。在本研究中,我们评估了2例GPS患者血小板的超微结构和细胞化学,以准确确定其细胞中缺少哪些细胞器。研究结果表明,灰色血小板的线粒体、致密体、过氧化物酶体和溶酶体数量正常,但特别缺乏α颗粒。对2例患者中1例的巨核细胞进行的初步研究表明,颗粒形成缺陷可能位于高尔基体区域水平。