Undiagnosed Behçet's Disease Complicated by Multiple Pseudoaneurysms and COVID-19 Infection.

IF 0.5 Q4 PERIPHERAL VASCULAR DISEASE International Journal of Angiology Pub Date : 2023-03-01 DOI:10.1055/s-0041-1735208
Aanchal Mehta, Julien Al Shakarchi, Lewis Meecham, Santhosh Vijay, Richard Downing
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Abstract

Behcet's disease (BD) is a rare multiorgan systemic disorder characterized by recurrent episodes of acute inflammation. Involvement of the vascular system, gastrointestinal tract, and central nervous system portends a poor prognosis. We report the case of a 54-year-old man who presented with a 2-week history of symptoms attributable to infrarenal aortic and left tibioperoneal trunk pseudoaneurysms, defined by CT angiography which also revealed right lower lobe pulmonary artery (PA) and right anterior tibial arterial aneurysms. A prior history of recurrent oral ulceration, periodic fever, cerebral venous sinus thrombosis, and aseptic endocarditis with pulmonary emboli invoked a diagnosis of BD. Immunosuppression was commenced immediately, following synchronous endovascular and open arterial intervention, except the PA aneurysm. He developed a fever and cough 8 days postoperatively as a consequence of COVID-19 infection from which he recovered without complications. The management of the patient's four aneurysms in different vascular territories and postoperative COVID-19 infection in the presence of mandatory immunosuppression are discussed.

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未确诊的behet病并发多发性假性动脉瘤和COVID-19感染。
白塞氏病(BD)是一种罕见的多器官全身性疾病,以急性炎症反复发作为特征。累及血管系统、胃肠道和中枢神经系统预示预后不良。我们报告一例54岁的男性患者,其表现为2周的肾下主动脉和左侧胫腓主干假性动脉瘤,CT血管造影显示右下叶肺动脉(PA)和右侧胫骨前动脉动脉瘤。既往有复发性口腔溃疡、周期性发热、脑静脉窦血栓形成和无菌性心内膜炎合并肺栓塞的病史,可诊断为BD。除PA动脉瘤外,在同步血管内和开放动脉介入治疗后立即开始免疫抑制。由于感染COVID-19,术后8天患者出现发烧和咳嗽,随后康复,无并发症。本文讨论了患者在不同血管区域的四个动脉瘤的处理以及强制性免疫抑制下的术后COVID-19感染。
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来源期刊
International Journal of Angiology
International Journal of Angiology PERIPHERAL VASCULAR DISEASE-
CiteScore
1.30
自引率
16.70%
发文量
57
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