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儿童免疫性血小板减少性紫癜诊断中的陷阱:4例报告

Pitfalls in the diagnosis of immune thrombocytopenic purpura in children: 4 case reports.

作者信息

Biner Betül, Devecioğlu Omer, Demir Muzaffer

机构信息

Department of Pediatrics, Division of Pediatric Hematology-Oncology, School of Medicine, Trakya University, Edirne, Turkey.

出版信息

Clin Appl Thromb Hemost. 2007 Jul;13(3):329-33. doi: 10.1177/1076029607302444.

Abstract

Acute idiopathic thrombocytopenic purpura is the most common cause of thrombocytopenia in childhood, and diagnosis of idiopathic thrombocytopenic purpura is made clinically based on the exclusion of other causes of thrombocytopenia. Patients with diverse causes of thrombocytopenia are sometimes erroneously diagnosed as having idiopathic thrombocytopenic purpura. However, for the prevention of misdiagnoses, careful inspection of peripheral blood smear is of utmost importance. This report presents 4 cases presumed as acute idiopathic thrombocytopenic purpura that were finally identified as pseudothrombocytopenia, inherited macrothrombocytopenia (MHY9 disorders) possibly Epstein syndrome, Bernard-Soulier syndrome, and drug-induced thrombocytopenia. They draw attention to the importance of platelet morphology to exclude inherited macrothrombocytopenia and history to exclude drug-induced thrombocytopenia. Better diagnostic approaches would be possible by the awareness of these relatively rare causes of isolated thrombocytopenia.

摘要

急性特发性血小板减少性紫癜是儿童血小板减少最常见的原因,特发性血小板减少性紫癜的诊断是在临床排除其他血小板减少原因的基础上做出的。多种原因导致血小板减少的患者有时会被错误地诊断为特发性血小板减少性紫癜。然而,为防止误诊,仔细检查外周血涂片至关重要。本报告介绍了4例最初疑似急性特发性血小板减少性紫癜的病例,最终确诊为假性血小板减少、遗传性巨大血小板减少症(MHY9相关疾病),可能为爱泼斯坦综合征、伯纳德-索利尔综合征以及药物性血小板减少症。这些病例提醒人们注意血小板形态对于排除遗传性巨大血小板减少症的重要性,以及用药史对于排除药物性血小板减少症的重要性。认识到这些相对罕见的孤立性血小板减少原因后,可能会有更好的诊断方法。

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