右髂总动脉破裂感染假性动脉瘤为深静脉血栓的罕见表现:1例报告并文献复习。

IF 0.8 Q4 PERIPHERAL VASCULAR DISEASE
Deshan Mario Gomez, Lumini Edirisuriya, Praneeth Athukorale, Thushan Gooneratne
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引用次数: 0

摘要

孤立性髂动脉假性动脉瘤极为罕见,通常无症状。然而,邻近结构如输尿管、肠或深静脉破裂或受压可能引起症状。46岁男性,右下肢肿胀,下腹部疼痛6个月。双工显像显示髂股深静脉血栓形成。血液检查显示中性粒细胞增多和炎症标志物升高。增强计算机断层扫描显示一个大的偏心,不规则的右髂总动脉假性动脉瘤伴肾积水,输尿管积水和下腔静脉压迫。根据影像学和生化检查,初步诊断为感染髂动脉假性动脉瘤。患者成功地接受了血管内支架移植。深静脉血栓形成是一种罕见的表现感染髂动脉假性动脉瘤。早期转诊和及时干预是实现最佳结果的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Uncommon Presentation of a Ruptured Right Common Iliac Artery Infected Pseudoaneurysm as Deep Vein Thrombosis: A Case Report and Literature Review.

Isolated iliac artery pseudoaneurysms are extremely rare and typically asymptomatic. However, symptoms may arise from rupture or compression of adjacent structures, such as the ureter, bowel or deep veins. A 46-year-old male presented with right lower limb swelling and preceding lower abdominal pain of 6 months. Duplex imaging showed iliofemoral deep vein thrombosis. Blood tests showed neutrophil leukocytosis and elevated inflammatory markers. Contrast-enhanced computed tomography demonstrated a large eccentric, irregular right common iliac artery pseudoaneurysm with hydronephrosis, hydroureter, and inferior vena cava compression. Based on the radiological and biochemical investigations, a tentative diagnosis of infected iliac artery pseudoaneurysm was made. The patient was successfully managed with endovascular stent grafting. Deep vein thrombosis is a rare presentation of a infected iliac artery pseudoaneurysm. Early referral and timely intervention are crucial for achieving optimal outcomes.

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来源期刊
CiteScore
1.10
自引率
11.10%
发文量
29
审稿时长
17 weeks
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