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儿童系统性红斑狼疮中的灾难性抗磷脂抗体综合征

Catastrophic antiphospholipid antibody syndrome in pediatric systemic lupus erythematosus.

作者信息

Falcini F, Taccetti G, Ermini M, Trapani S, Matucci Cerinic M

机构信息

Department of Pediatrics-Rheumatology Unit, Meyer Hospital, University of Florence, Italy.

出版信息

J Rheumatol. 1997 Feb;24(2):389-92.

PMID:9035002
Abstract

Catastrophic antiphospholipid antibody syndrome, reported in a minority of patients with circulating antiphospholipid antibodies, is characterized by widespread vascular occlusions. The term "catastrophic" has been used to describe the severity of symptomatology, sometimes leading to death. We describe a girl aged 11 years, fulfilling diagnostic criteria for systemic lupus erythematosus, with recurrent episodes of thromboembolic phenomena involving lung and skin, complicated with disseminated intravascular coagulation. Treatment with warfarin ultimately resulted in effective control of the disease.

摘要

灾难性抗磷脂抗体综合征在少数循环抗磷脂抗体阳性患者中被报道,其特征为广泛的血管闭塞。“灾难性”一词用于描述症状的严重程度,有时会导致死亡。我们描述了一名11岁女孩,符合系统性红斑狼疮的诊断标准,反复出现累及肺部和皮肤的血栓栓塞现象,并并发弥散性血管内凝血。华法林治疗最终有效控制了该疾病。

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引用本文的文献

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Catastrophic antiphospholipid antibody syndrome in a child with thrombotic microangiopathy.一名患有血栓性微血管病儿童的灾难性抗磷脂抗体综合征
Indian J Nephrol. 2012 Jul;22(4):310-3. doi: 10.4103/0971-4065.101266.
2
Microthrombotic/microangiopathic manifestations of the antiphospholipid syndrome.抗磷脂综合征的微血栓形成/微血管病表现
Clin Rev Allergy Immunol. 2009 Jun;36(2-3):109-25. doi: 10.1007/s12016-008-8104-z.
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Catastrophic antiphospholipid syndrome in a 7-year-old girl.一名7岁女童的灾难性抗磷脂综合征
Clin Rheumatol. 2007 Jun;26(6):1011-3. doi: 10.1007/s10067-006-0251-0. Epub 2006 Jul 6.
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Antiphospholipid syndrome associated with infections: clinical and microbiological characteristics of 100 patients.与感染相关的抗磷脂综合征:100例患者的临床和微生物学特征
Ann Rheum Dis. 2004 Oct;63(10):1312-7. doi: 10.1136/ard.2003.014175.