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一名患有甲型血友病的免疫缺陷患者的慢性血小板减少症。

Chronic thrombocytopenia in an immunodeficient patient with hemophilia A.

作者信息

Hach V, Bergmann L, Scharrer I, Mitrou P, Mueller-Eckhardt C

出版信息

Blut. 1985 May;50(5):293-8. doi: 10.1007/BF00319755.

Abstract

Coincident hemophilia and idiopathic thrombocytopenia has been rarely observed. We report here on a young man with severe hemophilia A who was treated with concentrates of lyophilized antihemophilic factor for several years before he developed thrombocytopenia. An isolated thrombocytopenia coincident with reduced platelet survival, ample megakaryocytes in the bone marrow, elevated platelet-associated IgG, as well as remission after treatment with prednisone and splenectomy, suggest the idiopathic form of thrombocytopenia. In addition, defects in cellular immunity became obvious. A causal relationship between the application of blood-derived products and the development of the platelet disorder as well as the impairment of the T-cell system remain to be demonstrated.

摘要

血友病与特发性血小板减少症同时出现的情况鲜有报道。我们在此报告一名患有严重甲型血友病的年轻男子,他在出现血小板减少症之前,接受冻干抗血友病因子浓缩物治疗数年。孤立性血小板减少症伴有血小板生存期缩短、骨髓中巨核细胞丰富、血小板相关IgG升高,以及泼尼松和脾切除治疗后病情缓解,提示为特发性血小板减少症。此外,细胞免疫缺陷变得明显。血液制品的应用与血小板疾病的发生以及T细胞系统损伤之间的因果关系仍有待证实。

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