Celada A
Scand J Haematol. 1982 Feb;28(2):169-74. doi: 10.1111/j.1600-0609.1982.tb00510.x.
A patient with thalassemia intermedia and haemosiderosis is reported. This patient did not receive transfusions or iron therapy. The iron absorption and the plasma iron turnover (PIT) were increased. Transfusions were carried out in order to decrease the amount of abnormal erythropoiesis. After that, the erythropoietin and PIT were decreased to normal levels and the iron absorption also returned to normal. The data presented suggest that increased erythropoiesis was responsible for the abnormally high iron absorption and subsequently for the haemosiderosis of the patient presented.
报告了一名中间型地中海贫血合并含铁血黄素沉着症的患者。该患者未接受输血或铁剂治疗。铁吸收和血浆铁周转率(PIT)增加。为减少异常红细胞生成进行了输血。此后,促红细胞生成素和PIT降至正常水平,铁吸收也恢复正常。所呈现的数据表明,红细胞生成增加是导致该患者铁吸收异常增高并进而导致含铁血黄素沉着症的原因。