Iolascon A, Martire B, Lee M J, Wickramasinghe S N
Dipartimento di Biomedicina dell'Età Evolutiva, Università degli Studi di Bari, Italy.
Eur J Haematol. 2000 Aug;65(2):140-3. doi: 10.1034/j.1600-0609.2000.9c227.x.
The congenital forms of dyserythropoiesis comprise a group of hereditary disorders characterized by ineffective erythropoiesis as the predominant mechanism of anaemia and morphologically abnormal erythroblasts. Up to now three major forms and four variants have been described. Group VII is characterized by dyserythropoiesis with intraerythroblastic precipitation of a non-globin protein. Here we described a case of dyserythropoietic anaemia presenting neonatally and requiring regular blood transfusions. Optical and electronic microscopy studies confirmed that this case was very similar to those in two previously reported transfusion-dependent patients with an unusual type of congenital dyserythropoietic anaemia.
先天性红细胞生成异常包括一组遗传性疾病,其特征是无效红细胞生成作为贫血的主要机制以及形态异常的成红细胞。到目前为止,已描述了三种主要形式和四种变体。VII组的特征是红细胞生成异常伴非珠蛋白在成红细胞内沉淀。我们在此描述了一例新生儿期出现的红细胞生成异常性贫血,需要定期输血。光学和电子显微镜研究证实,该病例与之前报道的两名依赖输血的先天性红细胞生成异常性贫血特殊类型患者的病例非常相似。