Cortelazzo S, Viero P, Casarotto C, D'Emilio A, Dini E, Barbui T
Scand J Haematol. 1984 Apr;32(4):403-10. doi: 10.1111/j.1600-0609.1984.tb00696.x.
80% of patients with chronic autoimmune thrombocytopenic purpura (ATP) may reach normalization of platelet count after steroids or splenectomy. In some of these cases a bleeding tendency may still persist and this has been attributed to abnormalities of platelet function resulting from the effect of platelet-bound antibodies. We have studied 49 ATP patients in order to assess the frequency and the pattern of this immune thrombopathia, and the correlation with the levels of platelet associated IgG (PAIgG). Only 3 patients (6%) had prolonged bleeding time and persistence of mucocutaneous haemorrhages, whereas 36% presented an altered platelet aggregation pattern. Platelet serotonin content, platelet and plasma beta-thromboglobulin concentration, and malondialdehyde generation after thrombin stimulus were found also altered, but the findings were not clearly correlated with the concentration of PAIgG.
80%的慢性自身免疫性血小板减少性紫癜(ATP)患者在使用类固醇或进行脾切除术后血小板计数可能恢复正常。在其中一些病例中,出血倾向可能仍然存在,这归因于血小板结合抗体作用导致的血小板功能异常。我们研究了49例ATP患者,以评估这种免疫性血小板病的发生率和模式,以及与血小板相关IgG(PAIgG)水平的相关性。只有3例患者(6%)出血时间延长且黏膜皮肤出血持续存在,而36%的患者呈现血小板聚集模式改变。还发现血小板5-羟色胺含量、血小板和血浆β-血小板球蛋白浓度以及凝血酶刺激后丙二醛生成均发生改变,但这些结果与PAIgG浓度并无明显相关性。