Grips K H, Ochs H, Otten H, Labedzki L, Tantow J
Dtsch Med Wochenschr. 1976 Sep 17;101(38):1389-92. doi: 10.1055/s-0028-1104279.
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.
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。