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发热伴血小板减少综合征、活化部分凝血活酶时间延长伴一过性抗磷脂抗体患者

A Patient with Severe Fever with Thrombocytopenia Syndrome, Activated Partial Thromboplastin Time Prolongation, and Transient Antiphospholipid Antibodies.

机构信息

Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Japan.

Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Japan.

出版信息

Intern Med. 2023 Jul 15;62(14):2145-2149. doi: 10.2169/internalmedicine.0782-22. Epub 2022 Dec 7.

Abstract

A prolonged activated partial thromboplastin time (APTT) is observed in patients with severe fever with thrombocytopenia syndrome (SFTS) and is one of the risk factors for severe disease. The mechanism underlying a prolonged APTT is largely unknown. The presence of antiphospholipid (aPL) antibodies in various viral infections has been documented but never reported in a patient with SFTS. We herein report the first SFTS patient with APTT prolongation and concurrent transiently positive aPL antibodies (lupus anticoagulants and anticardiolipin antibodies) with no coagulation factor deficiency.

摘要

在伴有发热伴血小板减少综合征(SFTS)的患者中,活化部分凝血活酶时间(APTT)延长较为常见,这是导致疾病加重的一个危险因素。APTT 延长的机制目前尚不清楚。在各种病毒感染中存在抗磷脂(aPL)抗体已被证实,但在 SFTS 患者中从未报道过。本研究报道了首例伴有 APTT 延长且无凝血因子缺乏的 SFTS 患者,其抗磷脂抗体(狼疮抗凝物和抗心磷脂抗体)一过性阳性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5187/10400393/2bfbd1245b8c/1349-7235-62-2145-g001.jpg

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