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Congenital dyserythropoietic anaemia with erythroblastic multinuclearity

机译:先天性贫血性贫血伴红细胞多核

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摘要

A case of congenital dyserythropoietic anaemia with erythroblastic multinuclearity in a 36-year-old woman is described and the literature reviewed. The syndrome is characterized by a protracted clinical course, a relatively mild anaemia, a low reticulocyte count, slight hyperbilirubinaemia, splenomegaly, pronounced erythroid hyperplasia with reversal of the myeloid erythroid ratio, and in particular by the presence of multinucleated erythroblasts in the marrow. The picture of ineffective erythropoiesis is confirmed by erythrokinetic studies. The present case is the forty-first to be described in the literature and is the third from Britain. Thirty-one of these have occurred in seven families but a family history has been lacking in the remaining ten. The onset of anaemia occurred in childhood in 21 of the 41 cases.
机译:描述了一例36岁女性先天性促红细胞生成贫血伴红细胞多核的情况,并复习了文献。该综合征的特点是临床病程延长,贫血相对较轻,网织红细胞数量少,轻度高胆红素血症,脾肿大,明显的红系增生和髓样红系比例逆转,特别是骨髓中存在多核成红细胞。促红细胞动力学研究证实了无效的促红细胞生成。本案是文献中描述的第41个案件,是英国的第三个案件。其中的三十一个发生在七个家庭中,而其余十个家庭则缺乏家族史。贫血的发作发生在儿童期的41例中的21例中。

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