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[肝源性多球蛋白血症和红细胞增多症]

[Hepatogenic polyglobulinemias and polycythemias].

作者信息

Hadnagy C, Sass G, Szabó Z

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1977;104(5):656-62.

PMID:75134
Abstract

The authors distinguish three kinds of hepatogenous polyglobulia: Polycythaemia caused by Budd-Chiari syndrome, polycythaemia caused by a Mosse syndrome (cirrhosis without liver venous thrombosis) and polyglobulia caused by liver tumours. In all three cases the same mechanism is likely to induce polycythaemia or polyglobulia respectively. In addition to the three cases of the Mosse syndrome published in 1966, the present paper deals with three cases of Budd-Chiari syndrome. Twice the Budd-Chiari syndrome was followed by a polycythaemia, once a Budd-Chiari syndrome was developed in the course of a polycythaemia vera.

摘要

作者区分了三种肝源性红细胞增多症

布-加综合征所致红细胞增多症、莫斯综合征(无肝静脉血栓形成的肝硬化)所致红细胞增多症以及肝肿瘤所致红细胞增多症。在这三种情况下,可能分别由相同的机制诱发红细胞增多症或红细胞增多。除了1966年发表的3例莫斯综合征病例外,本文还讨论了3例布-加综合征病例。2次布-加综合征之后出现了红细胞增多症,1次真性红细胞增多症病程中出现了布-加综合征。

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