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感染中的血管并发症:两例报告

Vascular Complications in Infection: A Report of Two Cases.

作者信息

Kanowski Victoria A L, Bhutia Sherab G

机构信息

Department of Surgery, Cairns Hospital, Cairns, Queensland, Australia.

Department of Vascular Surgery, Cairns Hospital, Cairns, Queensland, Australia.

出版信息

EJVES Vasc Forum. 2023 May 13;59:31-35. doi: 10.1016/j.ejvsvf.2023.05.005. eCollection 2023.

Abstract

INTRODUCTION

First described in 1937, Q fever remains a relatively new disease, with much to be learned about its presentation and diagnosis. Due to its role in the development of aortic aneurysms and vascular graft infections, its implications in the vascular domain have become increasingly reported. This is a report of two cases of vascular complications associated with oxiella burnetii infection, and the challenges in managing their unique presentations.

REPORTS

Case 1: A 70 year old man with a prosthetic aortobiiliac graft and past Q fever infection presented with acute sepsis. Abdominal computed tomography (CT) showed soft tissue thickening and stranding around the graft, and locules of gas within the vessel. Pelvic magnetic resonance imaging (MRI) revealed a chain of abscesses within the right gluteal region, of which aspirate grew and . Open explanation of the aortic graft and replacement by superficial femoral vein was performed. Tissue culture confirmed a polymicrobial infection, and PCR of the aortic wall and pre-aortic lymph node was positive for Q fever. He was treated for recrudescent Q fever infection with a good outcome and recovery. Case 2: A 73 year old man had an incidental abdominal aortic aneurysm (AAA) identified at the time of Q fever diagnosis. Following an incomplete course of doxycycline and hydroxychloroquine, the aneurysm rapidly progressed, leading to presentation with right flank pain. Fluorodeoxyglucose (FDG) positron emission tomography (PET) showed multiple foci of uptake within the aneurysm wall. Open AAA repair with a polyester graft was performed, with AAA tissue positive for Q fever on PCR. The operation was successful, with the patient continuing clearance therapy at time of writing.

DISCUSSION

Q fever infection poses serious implications for patients with vascular grafts and AAAs, and thus, should be considered in the differential diagnosis of mycotic aortic aneurysms and in aortic graft infections.

摘要

引言

Q热于1937年首次被描述,仍是一种相对较新的疾病,其临床表现和诊断仍有许多有待了解之处。由于其在主动脉瘤和血管移植感染发展中的作用,其在血管领域的影响越来越多地被报道。本文报告两例与伯氏考克斯体感染相关的血管并发症病例,以及处理其独特表现时所面临的挑战。

病例报告

病例1:一名70岁男性,有主动脉双髂动脉人工血管移植史且既往有Q热感染,出现急性脓毒症。腹部计算机断层扫描(CT)显示移植血管周围软组织增厚和条索状影,血管内有气体小腔。盆腔磁共振成像(MRI)显示右臀区域有一串脓肿,脓肿穿刺液培养出 和 。对主动脉移植血管进行了开放清创,并用人造股静脉进行了置换。组织培养证实为混合菌感染,主动脉壁和主动脉前淋巴结的聚合酶链反应(PCR)检测Q热呈阳性。他接受了复发性Q热感染治疗,效果良好并康复。病例2:一名73岁男性在诊断Q热时偶然发现腹主动脉瘤(AAA)。在接受了一个疗程不完整的强力霉素和羟氯喹治疗后,动脉瘤迅速进展,导致出现右胁腹疼痛。氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)显示动脉瘤壁内有多个摄取灶。对AAA进行了带聚酯人工血管的开放修复手术,AAA组织的PCR检测Q热呈阳性。手术成功,在撰写本文时患者仍在继续清除治疗。

讨论

Q热感染对血管移植患者和AAA患者具有严重影响,因此,在霉菌性主动脉瘤和主动脉移植感染的鉴别诊断中应予以考虑。

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