Hyman E S
Lancet. 1983 Jan 15;1(8316):91-5. doi: 10.1016/s0140-6736(83)91741-5.
A previously healthy 39-year-old woman presented with severe iron-deficiency anaemia, but she had lost no blood and her serum iron level was high. Her bone marrow was hypercellular with a predominance of erythroid elements and had no stainable iron deposits, but it also showed dyserythropoiesis and an excess of apparently normal plasma cells. IgM was demonstrated on her bone-marrow erythrocytes and their precursors. On azathioprine and prednisone therapy she had a complete clinical and haematological remission. The impaired iron transport and the associated dyserythropoiesis were probably due to an IgM-mediated autoimmune process. Diabetes mellitus, which first appeared during her anaemic illness, could also have been due to an autoimmune process. This is the first report of an iron-deficiency anaemia caused by a naturally acquired impairment of iron transport.
一名39岁既往健康的女性出现严重缺铁性贫血,但无失血情况且血清铁水平较高。她的骨髓细胞增多,以红系成分占优势,无可染色铁沉积,同时还表现出红细胞生成异常和明显正常的浆细胞增多。在她的骨髓红细胞及其前体细胞上检测到IgM。接受硫唑嘌呤和泼尼松治疗后,她获得了完全的临床和血液学缓解。铁转运受损及相关的红细胞生成异常可能是由IgM介导的自身免疫过程所致。糖尿病在她贫血患病期间首次出现,也可能是由自身免疫过程引起。这是关于自然获得性铁转运障碍导致缺铁性贫血的首例报道。