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一名12个月大患特发性血小板减少性紫癜患儿的抗磷脂抗体

Antiphospholipids antibodies in a 12-month-old presenting with idiopathic thrombocytopenic purpura.

作者信息

Nseir Bacel, Panicker Jyoti

机构信息

Department of Internal Medicine/Pediatrics, Northeastern Ohio Universities College of Medicine/Western Reserve Care System, Youngstown, Ohio, USA.

出版信息

Pediatr Hematol Oncol. 2008 Apr-May;25(3):233-5. doi: 10.1080/08880010701884733.

Abstract

A 12-month-old Caucasian female with a history of recurrent ear infections presented to the emergency room with petechiae, severe thrombocytopenia (4000/microL), and abnormally prolonged activated partial thromboplastin time. Further autoantibody investigation detected antinuclear antibodies, anti-double-stranded DNA, and antiphospholipid antibodies. Platelet count, in response to intravenous immunoglobulin infusion, increased to more than 100 x 10(3) plt/microL. At 6-month follow-up, no positive autoantibodies were detected.

摘要

一名有复发性耳部感染病史的12个月大的白种女性因出现瘀点、严重血小板减少(4000/微升)及活化部分凝血活酶时间异常延长而就诊于急诊室。进一步的自身抗体检测发现了抗核抗体、抗双链DNA抗体及抗磷脂抗体。静脉输注免疫球蛋白后,血小板计数升至超过100×10³/微升。在6个月的随访中,未检测到阳性自身抗体。

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