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儿童抗磷脂抗体相关的布加综合征:一例报告并文献复习

Budd-Chiari syndrome associated with antiphospholipid antibodies in a child: report of a case and review of the literature.

作者信息

Saca L F, Szer I S, Henar E, Nanjundiah P, Haddad Z H, Quismorio F P

机构信息

Department of Pediatrics, Los Angeles County, School of Medicine, CA.

出版信息

J Rheumatol. 1994 Mar;21(3):545-8.

PMID:8006900
Abstract

Budd-Chiari syndrome, hypertension, and thrombocytopenia developed in a 6-year-old girl as manifestations of primary antiphospholipid antibody syndrome (APS). She improved with systemic corticosteroid and anticoagulation therapy. Anticardiolipin antibodies were found in the patient, her mother and 3 siblings, suggesting the importance of genetic factors. The clinical features of an APS in children is reviewed.

摘要

一名6岁女孩出现布加综合征、高血压和血小板减少症,这些是原发性抗磷脂抗体综合征(APS)的表现。她通过全身皮质类固醇和抗凝治疗后病情好转。在该患者、其母亲和3个兄弟姐妹体内均发现了抗心磷脂抗体,提示遗传因素的重要性。本文对儿童APS的临床特征进行了综述。

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