Behcet's Syndrome Resembling Takayasu's Arteritis with the Distribution of Arterial Involvement: A Case Report and Literature Review.

IF 1.3 Q4 RHEUMATOLOGY European journal of rheumatology Pub Date : 2023-04-01 DOI:10.5152/eurjrheum.2023.22043
Gamze Akkuzu, Duygu Sevinç Özgür, Bilgin Karaalioğlu, Melek Yalçın Mutlu, Fatih Yıldırım, Mustafa Erdoğan, Burak İnce, Cemal Bes
{"title":"Behcet's Syndrome Resembling Takayasu's Arteritis with the Distribution of Arterial Involvement: A Case Report and Literature Review.","authors":"Gamze Akkuzu,&nbsp;Duygu Sevinç Özgür,&nbsp;Bilgin Karaalioğlu,&nbsp;Melek Yalçın Mutlu,&nbsp;Fatih Yıldırım,&nbsp;Mustafa Erdoğan,&nbsp;Burak İnce,&nbsp;Cemal Bes","doi":"10.5152/eurjrheum.2023.22043","DOIUrl":null,"url":null,"abstract":"<p><p>Behcet's syndrome is a variable vessel vasculitis characterized by recurrent oral and genital ulcers with concomitant skin, ocular, neurologic, gastrointestinal, and joint involvement. Herein, we present a patient who was diagnosed with Behcet's syndrome, which with magnetic resonance angiography showed occlusion of the right subclavian artery at the level of the thoracic outlet and reverse flow in the right vertebral artery consistent with subclavian steal syndrome. In addition, partial narrowing was noted in the left renal artery. The distribution of arterial involvement resembled Takayasu's arteritis, although the presence of mucocutaneous lesions, male gender, history of deep vein thrombosis, and HLA-B51 positivity favored a diagnosis of vasculo-Behçet's syndrome. We treated the patient with methylprednisolone and cyclophosphamide. After the regression of vascular inflammation with immunosuppressive therapy, stenting was performed in the left renal artery.</p>","PeriodicalId":12066,"journal":{"name":"European journal of rheumatology","volume":"10 2","pages":"62-66"},"PeriodicalIF":1.3000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/21/41/ejr-10-2-62.PMC10544313.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5152/eurjrheum.2023.22043","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Behcet's syndrome is a variable vessel vasculitis characterized by recurrent oral and genital ulcers with concomitant skin, ocular, neurologic, gastrointestinal, and joint involvement. Herein, we present a patient who was diagnosed with Behcet's syndrome, which with magnetic resonance angiography showed occlusion of the right subclavian artery at the level of the thoracic outlet and reverse flow in the right vertebral artery consistent with subclavian steal syndrome. In addition, partial narrowing was noted in the left renal artery. The distribution of arterial involvement resembled Takayasu's arteritis, although the presence of mucocutaneous lesions, male gender, history of deep vein thrombosis, and HLA-B51 positivity favored a diagnosis of vasculo-Behçet's syndrome. We treated the patient with methylprednisolone and cyclophosphamide. After the regression of vascular inflammation with immunosuppressive therapy, stenting was performed in the left renal artery.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
白塞氏综合征类似大动脉炎,动脉受累分布:一例报告和文献复习。
白塞综合征是一种可变血管血管炎,其特征是复发性口腔和生殖器溃疡,伴有皮肤、眼部、神经系统、胃肠道和关节受累。在此,我们介绍了一名被诊断为白塞综合征的患者,其磁共振血管造影术显示右侧锁骨下动脉在胸腔出口处闭塞,右侧椎动脉逆流与锁骨下盗血综合征一致。此外,左肾动脉出现部分狭窄。动脉受累的分布类似于大动脉炎,尽管存在粘膜皮肤病变、男性、深静脉血栓形成史和HLA-B51阳性有利于诊断血管-贝氏综合征。我们用甲基强的松龙和环磷酰胺治疗患者。在用免疫抑制治疗消退血管炎症后,在左肾动脉进行支架植入。
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 去求助
来源期刊
自引率
0.00%
发文量
56
审稿时长
7 weeks
期刊最新文献
Bullous Cutaneous Lupus Erythematosus and Class V Lupus Nephritis: Rare Concurrence. Comparison and Significance of Contrast-Enhanced Computed Tomographic Findings of Large-Vessel Vasculitis Before and After Treatment: Differences Between Takayasu Arteritis and Giant Cell Arteritis. Evaluation of Rheumatologists' Teledermatology Practices and Perspectives. Factors Associated with the Development of Anti-drug Antibodies to TNFi and the Consequences for Axial Spondyloarthritis: A Two-year Follow-up Study. Homeopathy for Rheumatological Diseases: A Systematic Review.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1