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[I型、II型、III型先天性红细胞生成异常性贫血(CDA)中的溶血及溶血机制]

[Hemolysis and hemolysis mechanisms in congenital dyserythropoietic anemia (CDA) of type I. II., III].

作者信息

Rhyner K, Möhr P, Straub P W

出版信息

Schweiz Med Wochenschr. 1975 Nov 22;105(47):1594.

PMID:1209228
Abstract

On the basis of clinical symptoms, bone marrow morphology, electronmicroscopy and serological tests congenital dyserythropoietic anemia (CDA) was diagnosed in 3 families and identified as CDA type I, II, III respectively. Aside from intramedullary hemolysis, members of all three families showed peripheral hemolysis, in some cases severe, which was mediated through splenic (in all types) and additional intravascular destruction in types I and II. The underlying cause of the peripheral hemolysis appears to be reduced deformability of erythrocytes, as documented by reduced filterability. The latter appears to be caused, at least in type II, by an increase in viscosity of the cytoplasm which in turn is probably related to increased susceptibility to oxidative injury leading to inclusion body formation. Splenectomy in one patient with CDA II led to a definite reduction of hemolysis and cessation of hemolytic crises.

摘要

根据临床症状、骨髓形态学、电子显微镜检查和血清学检测,在3个家族中诊断出先天性红细胞生成异常性贫血(CDA),并分别鉴定为Ⅰ型、Ⅱ型、Ⅲ型CDA。除了骨髓内溶血外,所有3个家族的成员均表现出外周溶血,在某些情况下较为严重,其通过脾脏(所有类型)介导,Ⅰ型和Ⅱ型还存在额外的血管内破坏。外周溶血的根本原因似乎是红细胞变形性降低,这可通过滤过率降低得到证明。后者至少在Ⅱ型中似乎是由细胞质粘度增加引起的,而细胞质粘度增加反过来可能与氧化损伤易感性增加有关,导致包涵体形成。1例Ⅱ型CDA患者行脾切除术后溶血明显减轻,溶血危象停止。

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