Catastrophic Antiphospholipid Syndrome Presenting as a Stroke in an 11-Year-Old with Lupus

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2022-05-13 DOI:10.1155/2022/7890566
B. Senken, A. Whitehead
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引用次数: 2

Abstract

Catastrophic antiphospholipid syndrome (CAPS) is an infrequent but feared life-threatening complication of antiphospholipid syndrome (APS). CAPS is characterized by the rapid development of numerous thromboses across multiple organs resulting in multiorgan failure. It is rare but well-documented in the adult population. In contrast, it is exceedingly uncommon in pediatric patients and therefore not yet well described in the pediatric literature. Early recognition of APS is of the utmost importance to provide timely and effective management for a positive outcome. We present the case of an 11-year-old girl with history of systemic lupus erythematosus (SLE) and hypertension (HTN) who presented with acute onset altered mental status, found to have a large ischemic middle cerebral artery (MCA) and anterior cerebral artery (ACA) stroke as well as multiple, diffuse, and smaller ischemic lesions in the frontal lobe and cerebellum. Her presentation was further complicated by thrombocytopenia and renal and splenic infarction, as well as thrombosis of the right brachial vein consistent with a diagnosis of CAPS.
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灾难性抗磷脂综合征表现为11岁狼疮患者的中风
灾难性抗磷脂综合征(CAPS)是抗磷脂综合征(APS)中一种罕见但令人担忧的危及生命的并发症。CAPS的特点是跨多个器官的大量血栓的快速发展导致多器官衰竭。这是罕见的,但在成年人中有充分的记录。相比之下,它在儿科患者中非常罕见,因此尚未在儿科文献中得到很好的描述。早期识别APS对于提供及时有效的管理以获得积极的结果至关重要。我们报告一名患有系统性红斑狼疮(SLE)和高血压(HTN)病史的11岁女孩,表现为急性发作的精神状态改变,发现有一个大的缺血性大脑中动脉(MCA)和大脑前动脉(ACA)中风,以及额叶和小脑的多发,弥漫性和较小的缺血性病变。她的表现进一步复杂化了血小板减少,肾和脾梗死,以及右臂静脉血栓形成,与CAPS的诊断一致。
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来源期刊
自引率
11.10%
发文量
48
审稿时长
13 weeks
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