Blecher T E
Haematology Department, University Hospital, Nottingham.
Clin Lab Haematol. 1988;10(4):403-8. doi: 10.1111/j.1365-2257.1988.tb01188.x.
The case is presented of an elderly man in whom hereditary spherocytosis (HS) had been diagnosed many years previously. He also had diverticulitis and was referred because of increasing anaemia (Hb 7.7 g/dl). He was suffering from diarrhoea and anorexia, and was taking a very poor diet. Serum investigations showed low folate and vitamin B12 levels. His blood film, despite the history of HS, showed very few spherocytes, and the red cell osmotic fragility curve was virtually normal. Instead, the blood film showed normocytes and oval macrocytes, mostly with normal central pallor. He was treated with vitamin B12 injections and folic acid tablets. On this treatment, the Hb rapidly rose, the macrocytosis disappeared, the film appearances reverted to the classical picture of HS with large numbers of microspherocytes, and the osmotic fragility curve to the picture of markedly increased fragility typical of HS.
本文介绍了一位老年男性病例,多年前他被诊断患有遗传性球形红细胞增多症(HS)。他还患有憩室炎,因贫血加重(血红蛋白7.7g/dl)前来就诊。他有腹泻和厌食症状,饮食很差。血清检查显示叶酸和维生素B12水平较低。尽管有HS病史,他的血涂片显示球形红细胞很少,红细胞渗透脆性曲线基本正常。相反,血涂片显示正细胞和椭圆形大红细胞,大多中央淡染正常。他接受了维生素B12注射和叶酸片治疗。经过这种治疗,血红蛋白迅速上升,大红细胞症消失,血涂片表现恢复为HS的典型表现,即有大量小球形红细胞,渗透脆性曲线呈现HS典型的明显增加的脆性表现。