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再生障碍性贫血与胸腺瘤

[Aplastic anaemia and thymonal].

作者信息

Grips K H, Ochs H, Otten H, Labedzki L, Tantow J

出版信息

Dtsch Med Wochenschr. 1976 Sep 17;101(38):1389-92. doi: 10.1055/s-0028-1104279.

Abstract

The combination of aplastic anaemia and thymona was observed in a 49-year old woman. Concomitant with severe normochromic anaemia and reticulocytopenia was a cell-rich bone marrow smear in which erythropoietic precursors were almost absent. Immunological phenomena could not be demonstrated. The erythropoietin level was maximally increased. Pathological anatomy typically revealed a predominantly spindle-cell thymonal with only minor capsular invasion.

摘要

一名49岁女性被观察到患有再生障碍性贫血合并胸腺瘤。同时伴有严重的正色素性贫血和网织红细胞减少,骨髓涂片细胞丰富,但几乎没有红细胞生成前体细胞。未发现免疫现象。促红细胞生成素水平大幅升高。病理解剖显示典型的主要为梭形细胞胸腺瘤,仅有轻微的包膜侵犯。

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[Aplastic anaemia and thymonal].再生障碍性贫血与胸腺瘤
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Aplastic anaemia: autoimmune sequel of thymoma.再生障碍性贫血:胸腺瘤的自身免疫性后遗症。
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