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成人血友病患者血小板减少症的成功保守治疗

Successful conservative management of thrombocytopenia in adult hemophiliacs.

作者信息

Goldsmith J C, Kisker C T

机构信息

Department of Medicine, University of Nebraska, Omaha.

出版信息

Transfusion. 1988 Jan-Feb;28(1):68-9. doi: 10.1046/j.1537-2995.1988.28188127958.x.

Abstract

Hematologic abnormalities, including thrombocytopenia, have been reported in persons with acquired immune deficiency syndrome and in hemophiliacs. Seven of 92 adult hemophiliacs followed in a comprehensive hemophilia center developed mild to moderately severe thrombocytopenia in 1983. All had benign courses. None required therapy for thrombocytopenia, although several had increased cutaneous bleeding. Infection with human immunodeficiency virus may be important in the pathogenesis of these patients' thrombocytopenia as it has been in that of homosexual men.

摘要

据报道,获得性免疫缺陷综合征患者和血友病患者存在血液学异常,包括血小板减少症。1983年,在一家综合性血友病中心随访的92名成年血友病患者中,有7人出现了轻度至中度严重的血小板减少症。所有患者病程均为良性。尽管有几名患者皮肤出血有所增加,但无人因血小板减少症接受治疗。人类免疫缺陷病毒感染在这些患者血小板减少症的发病机制中可能很重要,就像在同性恋男性中一样。

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