医学
抗磷脂综合征
内科学
痹症科
冲程(发动机)
狼疮抗凝剂
抗体
自身抗体
血栓形成
胃肠病学
儿科
免疫学
机械工程
工程类
作者
Silvia Mancuso,Manuela De Michele,Simona Truglia,Antonella Capozzi,L. Rapino,Irene Berto,Cristiano Alessandri,Danilo Toni,Valeria Manganelli,Maurizio Sorice,Flavia Conti
出处
期刊:Reumatismo
[PAGEPress (Italy)]
日期:2024-09-25
标识
DOI:10.4081/reumatismo.2024.1701
摘要
Cerebrovascular events (CE) are one of the most common and severe events in antiphospholipid syndrome (APS), a condition characterized by thrombosis and circulating anti-phospholipid antibodies (aPL). Seronegative APS (SN-APS) refers to a group of patients with clinical features of APS but persistently negative tests for “criteria aPL”: anti-cardiolipin antibodies (aCL) and anti-β2glycoprotein I antibodies detected by enzyme-linked immunosorbent assay (ELISA), and the lupus anticoagulant detected by clotting assays. We report a series of five cases of SN-APS in young or middle-aged patients who tested positive for “non-criteria” aPL. We retrospectively collected cases of SN-APS patients who experienced CE without an identified cause despite an extensive diagnostic work-up and tested negative for criteria aPL. All the patient sera were tested for aCL by immunostaining on thin-layer chromatography (TLC) and anti-vimentin/cardiolipin (aCL/Vim) by ELISA. We identified five cases of female patients aged 21 to 58 years, evaluated at the Rheumatology Unit and/or Stroke Unit/Emergency Department of the Sapienza University Hospital of Rome, “Policlinico Umberto I”. All patients presented a clinical history suggestive of APS. All the patients tested positive for aCL by TLC-immunostaining, and one patient was positive for aCL/Vim. In young or middle-aged patients with cryptogenic CE and a clinical history suggestive of APS, the use of new diagnostic tools for identifying aPL, if validated in future studies, could represent an important step in the prompt diagnosis of APS.
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