Posttransfusion purpura secondary to an alloantibody reactive with HPA-5a (Brb)

被引:13
作者
Anolik, JH
Blumberg, N
Snider, J
Francis, CW
机构
[1] Univ Rochester, Sch Med & Dent, Rheumat & Immunol Unit, Rochester, NY 14627 USA
[2] Univ Rochester, Sch Med & Dent, Vasc Med Unit, Dept Med, Rochester, NY 14627 USA
[3] Univ Rochester, Sch Med & Dent, Dept Pathol & Lab Med, Rochester, NY 14627 USA
[4] Univ Rochester, Sch Med & Dent, Dept Cardiothorac Surg, Rochester, NY 14627 USA
关键词
D O I
10.1046/j.1537-2995.2001.41050633.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Posttransfusion purpura (PTP) is characterized by severe thrombocytopenia following blood transfusion that results from alloimmunization to platelet-specific alloantigens. Most cases involve antibodies against HPA-1a in homozygous HPA-1b persons. CASE REPORT: A patient developed PTP after cardiopulmonary bypass associated with a platelet-specific antibody with strong reactivity against HPA-5a (Br-b). Genotyping confirmed that the patient was homozygous for HPA-5b. CONCLUSION: This is the first well-documented occurrence of PTP associated with isolated allosensitization to HPA-5a or Br-b. The case highlights the importance of maintaining a high level of suspicion for PTP in the appropriate clinical setting, even in an atypical patient.
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收藏
页码:633 / 636
页数:4
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