首页> 美国卫生研究院文献>Case Reports in Cardiology >Infectious Aortitis with Abdominal Aortic Aneurysm in a 47-Year-Old Female with Systemic Lupus Erythematosus
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Infectious Aortitis with Abdominal Aortic Aneurysm in a 47-Year-Old Female with Systemic Lupus Erythematosus

机译:47岁系统性红斑狼疮女性的感染性主动脉炎与腹主动脉瘤。

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摘要

Aortic aneurysms are not commonly reported among patients with systemic lupus erythematosus (SLE). We report a case of a 47-year-old Filipino female diagnosed with SLE 17 years ago maintained on prolonged oral steroids, azathioprine, and hydroxychloroquine. She also had lupus nephritis, secondary hypertension, and dyslipidemia. She initially presented with a week-long watery nonbloody diarrhea with associated diffuse crampy abdominal pain and generalized weakness. She was admitted for a week at a provincial hospital and was given an unrecalled antibiotic with resolution of symptoms. Upon discharge, however, she experienced two weeks of severe right lower quadrant pain radiating to the back and left lower quadrant, with no history of diarrhea, vomiting, dysuria, and fever. Complete blood count showed slight leukocytosis and elevated C-reactive protein. Abdominal imaging revealed a saccular infrarenal aneurysm with dissection. An atherosclerotic mechanism was primarily considered, but a vasculitic process was likewise considered due to elevated acute phase reactants. The initial plan was Endovascular Aneurysm Repair (EVAR) but due to financial limitations, an exploratory laparotomy with infrarenal endoaneurysmorrhaphy was eventually performed. Intraoperative findings were a saccular infrarenal aneurysm with dissection up to the proximal right common iliac artery and an abscess compartment within the false lumen in the anterior aortic wall. Abscess culture yielded high growth of Salmonella group B. Micrographs of the aortic wall biopsy showed fibrin deposition necrosis and calcification with peripheral viable cellular infiltrates consisting of neutrophils and foamy macrophages. Inadvertently placing an endovascular graft in an infected aortic aneurysm would have led to graft infection and catastrophic morbidity. We highlight the significance of having a high index of suspicion for infectious causes of aortitis among immunocompromised patients presenting with aneurysm prior to pursuing an endovascular versus an open approach for repair.
机译:系统性红斑狼疮(SLE)患者中主动脉瘤不常见。我们报告一例17年前诊断为SLE的47岁菲律宾女性,长期服用口服类固醇,硫唑嘌呤和羟氯喹。她还患有狼疮肾炎,继发性高血压和血脂异常。她最初出现为期一周的水样非血性腹泻,伴有弥漫性痉挛性腹痛和全身无力。她在一家省立医院住院了一个星期,并服用了一种无法缓解症状的抗生素。然而,出院后,她经历了两周严重的右下腹疼痛,放射到背部和左下腹,没有腹泻,呕吐,排尿困难和发烧的病史。全血细胞计数显示轻度白细胞增多和C反应蛋白升高。腹部影像学检查发现囊状肾下动脉瘤并夹层。主要考虑了动脉粥样硬化的机制,但是由于急性期反应物的升高,同样考虑了血管形成过程。最初的计划是血管内动脉瘤修补术(EVAR),但由于经济上的限制,最终进行了探索性剖腹手术并进行了肾下动脉内麻醉。术中发现的是囊状肾下动脉瘤,直至右right总动脉近端均已解剖,主动脉前壁假腔内有脓肿腔。脓肿培养产生沙门氏菌B组的高生长。主动脉壁活检的显微照片显示纤维蛋白沉积坏死和钙化,周围有活细胞浸润,由中性粒细胞和泡沫巨噬细胞组成。无意中将血管内移植物置于感染的主动脉瘤中会导致移植物感染和灾难性发病。我们强调了在寻求血管内治疗之前与开放性修复方法相比,在患有动脉瘤的免疫受损患者中,对主动脉炎的感染原因具有高度怀疑的重要性。

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