Bird G W, Wingham J, Richardson S G
Haematologia (Budap). 1985;18(2):99-103.
A patient with myelofibrosis was studied for about four years. During this period he developed autoimmune haemolytic anaemia, a rare complication of myelofibrosis. Furthermore, about two years after the investigation started, his red blood cells, previously normal, became Tn-polyagglutinable, a change known to be due to somatic mutation in haemopoietic stem cells.
对一名骨髓纤维化患者进行了约四年的研究。在此期间,他患上了自身免疫性溶血性贫血,这是骨髓纤维化的一种罕见并发症。此外,在研究开始约两年后,他之前正常的红细胞变成了Tn多凝集性的,这种变化已知是由于造血干细胞的体细胞突变所致。