SYNDROME DES ANTIPHOSPHOLIPIES. À PROPOS DE 30 CAS.

Olga Nahas, Lina Serhal, Myrna Germanos, Stéphanie Abou Nakad, Georges Maalouly, Fady Haddad, Aline TohmÉ
{"title":"SYNDROME DES ANTIPHOSPHOLIPIES. À PROPOS DE 30 CAS.","authors":"Olga Nahas,&nbsp;Lina Serhal,&nbsp;Myrna Germanos,&nbsp;Stéphanie Abou Nakad,&nbsp;Georges Maalouly,&nbsp;Fady Haddad,&nbsp;Aline TohmÉ","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To analyze clinical and immuno- logic manifestations of Lebanese patients with the antiphos- pholipid syndrome (APS).</p><p><strong>Patients and methods: </strong>Our study was retrospective and was done on hospitalized patients be- tween 2001 and 2013. All these patients fulfilled the interna- tional criteria for diagnosis (Sydney criteria).</p><p><strong>Results: </strong>Of the 30 patients selected, we noticed a female predominance (sex ratio: 2.75). The age at diagnosis ranged between 9 and 72 years with a mean age of 43 - 17 years. \"Primary\" APS was present in 70% of patients; APS was associated with systemic lupus erythematosus (SLE) in 23% of patients, with a mixed connective tissue disease in 3% and systemic vasculitis in 3%. A catastrophic APS occurred in 3 cases (10%). The most com- mon presenting manifestations were deep venous thrombosis (53%), pulmonary embolism (33%) and stroke (13%). Eleven patients (37%) had venous thrombosis, 7 (23%) had arterial thrombosis alone and 7 (23%) both arterial and venous throm- bosis. Deep venous thrombosis occurred mostly in the lower limbs (70%) whereas arterial thrombosis occurred in cerebral arteries in 50% of cases. The most common fetal complica- tions were early fetal loss (62.5%). Anticardiolipin antibodies were the most frequently identified antibodies (83%), followed by anti-p2GPI (70%) and anticoagulant lupus (11%). An effec- tive anticoagulation by anti-vitamin K was performed in 29 pa- tients. Corticosteroids were prescribed in 13 cases and were associated to immunosuppressant drugs in 6 cases of second- ary APS and the 3 catastrophic APS. The patients with cat- astrophic APS received also intravenous immunoglobulin. Response to treatment was favorable in 86% of patients with a mean follow up of 6 4 years. We deplored 4 deaths, 2 with- in the catastrophic APS.</p><p><strong>Conclusion: </strong>The APS does not seem to have particular features in Lebanon. The primary form seems to be the most common. It is important to diagnose this syn- drome earlier before the onset of serious complications.</p>","PeriodicalId":430072,"journal":{"name":"Le Journal médical libanais. The Lebanese medical journal","volume":"64 2","pages":"78-83"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Le Journal médical libanais. The Lebanese medical journal","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: To analyze clinical and immuno- logic manifestations of Lebanese patients with the antiphos- pholipid syndrome (APS).

Patients and methods: Our study was retrospective and was done on hospitalized patients be- tween 2001 and 2013. All these patients fulfilled the interna- tional criteria for diagnosis (Sydney criteria).

Results: Of the 30 patients selected, we noticed a female predominance (sex ratio: 2.75). The age at diagnosis ranged between 9 and 72 years with a mean age of 43 - 17 years. "Primary" APS was present in 70% of patients; APS was associated with systemic lupus erythematosus (SLE) in 23% of patients, with a mixed connective tissue disease in 3% and systemic vasculitis in 3%. A catastrophic APS occurred in 3 cases (10%). The most com- mon presenting manifestations were deep venous thrombosis (53%), pulmonary embolism (33%) and stroke (13%). Eleven patients (37%) had venous thrombosis, 7 (23%) had arterial thrombosis alone and 7 (23%) both arterial and venous throm- bosis. Deep venous thrombosis occurred mostly in the lower limbs (70%) whereas arterial thrombosis occurred in cerebral arteries in 50% of cases. The most common fetal complica- tions were early fetal loss (62.5%). Anticardiolipin antibodies were the most frequently identified antibodies (83%), followed by anti-p2GPI (70%) and anticoagulant lupus (11%). An effec- tive anticoagulation by anti-vitamin K was performed in 29 pa- tients. Corticosteroids were prescribed in 13 cases and were associated to immunosuppressant drugs in 6 cases of second- ary APS and the 3 catastrophic APS. The patients with cat- astrophic APS received also intravenous immunoglobulin. Response to treatment was favorable in 86% of patients with a mean follow up of 6 4 years. We deplored 4 deaths, 2 with- in the catastrophic APS.

Conclusion: The APS does not seem to have particular features in Lebanon. The primary form seems to be the most common. It is important to diagnose this syn- drome earlier before the onset of serious complications.

抗磷脂综合征。大约30个案例。
目的:分析黎巴嫩抗磷-磷脂综合征(APS)患者的临床和免疫学表现。患者和方法:我们的研究是回顾性的,研究对象是2001年至2013年住院的患者。所有患者均符合国际诊断标准(悉尼标准)。结果:在入选的30例患者中,我们注意到女性占优势(性别比:2.75)。诊断年龄在9 - 72岁之间,平均年龄为43 - 17岁。70%的患者存在“原发性”APS;23%的APS患者与系统性红斑狼疮(SLE)相关,3%的患者伴有混合性结缔组织病,3%的患者伴有系统性血管炎。3例(10%)发生灾难性APS。最常见的表现是深静脉血栓形成(53%)、肺栓塞(33%)和脑卒中(13%)。有静脉血栓11例(37%),单发动脉血栓7例(23%),动脉和静脉合并血栓7例(23%)。深静脉血栓主要发生在下肢(70%),动脉血栓发生在脑动脉(50%)。最常见的胎儿并发症是早期胎儿丢失(62.5%)。抗心磷脂抗体是最常见的抗体(83%),其次是抗p2gpi抗体(70%)和抗凝狼疮抗体(11%)。对29例患者行抗维生素K有效抗凝治疗。13例患者使用皮质类固醇,6例继发性APS和3例灾难性APS患者同时使用免疫抑制剂。猫萎缩性APS患者同时静脉注射免疫球蛋白。86%的患者对治疗反应良好,平均随访64年。我们哀悼4人死亡,其中2人死于APS。结论:APS在黎巴嫩似乎没有特殊的特征。初级形式似乎是最常见的。在出现严重并发症之前及早诊断这种综合征是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信