Hewitt P, Davies S, Cohen H, Machin S
Acta Haematol. 1984;71(5):345-9. doi: 10.1159/000206613.
A patient with a 20-year history of Waldenström's hypergammaglobulinaemic purpura has over that time developed increasingly troublesome clinical symptoms of purpura and joint swelling, associated with a progressive increase in the level of polyclonal IgG. These symptoms have been controlled by the use of a regular plasmapheresis regime and associated with a reduction in IgG levels.
一位患有瓦尔登斯特伦高丙种球蛋白血症性紫癜20年的患者,在此期间紫癜和关节肿胀的临床症状日益严重,同时多克隆IgG水平逐渐升高。这些症状通过定期进行血浆置换疗法得到了控制,且IgG水平有所降低。