Cryptogenic stroke and seronegative antiphospholipid syndrome: a case series of patients with positivity for "non-criteria" antiphospholipid antibodies.

IF 1.2 Q4 RHEUMATOLOGY
S Mancuso, M De Michele, S Truglia, A Capozzi, L Rapino, I Berto, C Alessandri, D Toni, V Manganelli, M Sorice, F Conti
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引用次数: 0

Abstract

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.

隐源性中风与血清阴性抗磷脂综合征:"非标准 "抗磷脂抗体阳性患者的病例系列。
脑血管事件(CE)是抗磷脂综合征(APS)最常见和最严重的事件之一,APS是一种以血栓形成和循环抗磷脂抗体(aPL)为特征的疾病。血清阴性 APS(SN-APS)是指一组具有 APS 临床特征但 "标准 aPL "检测持续阴性的患者:通过酶联免疫吸附试验(ELISA)检测抗心磷脂抗体(aCL)和抗β2 糖蛋白 I 抗体,以及通过凝血试验检测狼疮抗凝物。我们报告了一组五例 SN-APS 病例,这些患者均为中青年,且 aPL 检测呈 "非标准 "阳性。我们回顾性地收集了一些 SN-APS 患者的病例,这些患者虽然经过了广泛的诊断检查,但在没有明确病因的情况下发生了 CE,而且标准 aPL 检测呈阴性。所有患者血清均通过薄层色谱(TLC)免疫染色法检测 aCL,通过 ELISA 检测抗波形蛋白/心磷脂(aCL/Vim)。我们发现了五例年龄在 21 至 58 岁之间的女性患者,她们都曾在罗马萨皮恩扎大学医院("Policlinico Umberto I")风湿病科和/或卒中科/急诊科接受过评估。所有患者均有提示 APS 的临床病史。通过 TLC 免疫染色,所有患者的 aCL 检测结果均呈阳性,其中一名患者的 aCL/Vim 检测结果呈阳性。对于隐源性 CE 和临床病史提示 APS 的年轻或中年患者,使用新的诊断工具识别 aPL(如果在未来的研究中得到验证)可能是迅速诊断 APS 的重要一步。
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来源期刊
Reumatismo
Reumatismo RHEUMATOLOGY-
CiteScore
2.10
自引率
7.10%
发文量
20
审稿时长
10 weeks
期刊介绍: Reumatismo is the official Journal of the Italian Society of Rheumatology (SIR). It publishes Abstracts and Proceedings of Italian Congresses and original papers concerning rheumatology. Reumatismo is published quarterly and is sent free of charge to the Members of the SIR who regularly pay the annual fee. Those who are not Members of the SIR as well as Corporations and Institutions may also subscribe to the Journal.
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