抗磷脂抗体综合征导致的半舌缺血--病例报告

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL

Journal of Community Hospital Internal Medicine Perspectives Pub Date : 2024-09-09 eCollection Date: 2024-01-01 DOI:10.55729/2000-9666.1385

Ateeb U Rahman, Amir S Kazi, Ali A Asif, Amna Chaudary

{"title":"抗磷脂抗体综合征导致的半舌缺血--病例报告","authors":"Ateeb U Rahman, Amir S Kazi, Ali A Asif, Amna Chaudary","doi":"10.55729/2000-9666.1385","DOIUrl":null,"url":null,"abstract":"Antiphospholipid antibody syndrome, also known as Hughes syndrome, is a multi-system autoimmune disorder characterized by recurrent thrombosis and fetal loss. The most common types of antiphospholipid antibodies include lupus anticoagulants, anticardiolipin antibodies, and anti-beta 2 glycoprotein 1 antibodies. Owing to the prothrombotic nature of this disease, diagnosing and treating the condition as early as possible is necessary. In this case report, we discuss the typical and atypical manifestations of this disease, as well as the current diagnostic and therapeutic options. We present a case of atypical antiphospholipid antibody syndrome in the form of hemi-tongue ischemia.","PeriodicalId":15460,"journal":{"name":"Journal of Community Hospital Internal Medicine Perspectives","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466327/pdf/","citationCount":"0","resultStr":"{\"title\":\"Hemi-tongue Ischemia Due to Antiphospholipid Antibody Syndrome-A Case Report.\",\"authors\":\"Ateeb U Rahman, Amir S Kazi, Ali A Asif, Amna Chaudary\",\"doi\":\"10.55729/2000-9666.1385\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Antiphospholipid antibody syndrome, also known as Hughes syndrome, is a multi-system autoimmune disorder characterized by recurrent thrombosis and fetal loss. The most common types of antiphospholipid antibodies include lupus anticoagulants, anticardiolipin antibodies, and anti-beta 2 glycoprotein 1 antibodies. Owing to the prothrombotic nature of this disease, diagnosing and treating the condition as early as possible is necessary. In this case report, we discuss the typical and atypical manifestations of this disease, as well as the current diagnostic and therapeutic options. We present a case of atypical antiphospholipid antibody syndrome in the form of hemi-tongue ischemia.\",\"PeriodicalId\":15460,\"journal\":{\"name\":\"Journal of Community Hospital Internal Medicine Perspectives\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2024-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466327/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Community Hospital Internal Medicine Perspectives\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55729/2000-9666.1385\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Community Hospital Internal Medicine Perspectives","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55729/2000-9666.1385","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}

引用次数: 0

摘要

抗磷脂抗体综合征又称休斯综合征，是一种多系统自身免疫性疾病，以反复发生血栓形成和胎儿死亡为特征。最常见的抗磷脂抗体类型包括狼疮抗凝物、抗心磷脂抗体和抗β2糖蛋白1抗体。由于这种疾病具有促血栓形成的性质，因此必须尽早诊断和治疗。在本病例报告中，我们将讨论这种疾病的典型和非典型表现，以及目前的诊断和治疗方案。我们介绍了一例半舌缺血型非典型抗磷脂抗体综合征病例。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Hemi-tongue Ischemia Due to Antiphospholipid Antibody Syndrome-A Case Report.

Antiphospholipid antibody syndrome, also known as Hughes syndrome, is a multi-system autoimmune disorder characterized by recurrent thrombosis and fetal loss. The most common types of antiphospholipid antibodies include lupus anticoagulants, anticardiolipin antibodies, and anti-beta 2 glycoprotein 1 antibodies. Owing to the prothrombotic nature of this disease, diagnosing and treating the condition as early as possible is necessary. In this case report, we discuss the typical and atypical manifestations of this disease, as well as the current diagnostic and therapeutic options. We present a case of atypical antiphospholipid antibody syndrome in the form of hemi-tongue ischemia.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of Community Hospital Internal Medicine Perspectives MEDICINE, GENERAL & INTERNAL-

自引率

0.00%

发文量

106

审稿时长

17 weeks

期刊介绍： JCHIMP provides: up-to-date information in the field of Internal Medicine to community hospital medical professionals a platform for clinical faculty, residents, and medical students to publish research relevant to community hospital programs. Manuscripts that explore aspects of medicine at community hospitals welcome, including but not limited to: the best practices of community academic programs community hospital-based research opinion and insight from community hospital leadership and faculty the scholarly work of residents and medical students affiliated with community hospitals.