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一名女性特发性血小板减少性紫癜的典型病例,表现为自发性瘀斑。

A classic case of ITP in a woman presenting with spontaneous bruising.

作者信息

Doneza Janine, Hirota Sean, Tokeshi Jinichi

机构信息

University of Hawai'i, John A. Burns School of Medicine, Honolulu, HI, USA.

出版信息

Hawaii Med J. 2008 Nov;67(11):292-3.

PMID:19226909
Abstract

Idiopathic thrombocytopenic purpura is an autoimmune disorder causing thrombocytopenia. The authors present the case of a patient who presented with spontaneous bruising. A complete blood cell count revealed the patient was severely thrombocytopenic with a platelet count of 4000. Further evaluation failed to reveal a cause for thrombocytopenia and the patient was subsequently diagnosed with idiopathic thrombocytopenic purpura.

摘要

特发性血小板减少性紫癜是一种导致血小板减少的自身免疫性疾病。作者报告了一例出现自发性瘀伤的患者。全血细胞计数显示该患者严重血小板减少,血小板计数为4000。进一步评估未能发现血小板减少的原因,该患者随后被诊断为特发性血小板减少性紫癜。

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