双侧并发股深动脉瘤:1例罕见外周动脉瘤。

IF 0.4 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2024-12-30 eCollection Date: 2025-01-01 DOI:10.1093/jscr/rjae821
Rahel Abebayehu Assefa, Henok T/Silassie Zeleke, Dawit G/Giorgis
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引用次数: 0

摘要

股深动脉瘤非常罕见;特别是当分离并同时发生在四肢时。我们报告这样的情况下,误诊16岁的男性提出血肿后,试图疏散疼痛肿胀在左腹股沟。一旦通过计算机断层血管造影(CTA)确诊,就对左肢体进行急诊动脉瘤切除术并结扎股深动脉(DFA)。随后,在同一入院期间,对侧肢体行选择性动脉瘤切除术并DFA结扎,无术后并发症。超声心动图,怀疑感染性心内膜炎可能是真菌性动脉瘤的原因,显示慢性风湿性心瓣膜病,没有植被、脓肿或心内血栓的证据。本病例报告旨在讨论患者的临床表现、CTA表现和在低资源环境下的手术处理,强调这种罕见疾病如果误诊的风险。
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Simultaneous bilateral deep femoral artery aneurysms: case report of a rare peripheral arterial aneurysm.

Deep femoral artery aneurysms are very rare; particularly when isolated and occur simultaneously in both limbs. We report such a case of a misdiagnosed 16-year-old male presenting after hematoma evacuation was attempted for painful swelling in the left groin. Once the diagnosis was confirmed by computed tomography angiography (CTA), an emergency aneurysmectomy with deep femoral artery (DFA) ligation was performed on the left limb. Subsequently, an elective aneurysmectomy with DFA ligation was done for the contralateral limb during the same admission, with no postoperative complications. Echocardiography, performed with suspicion for infective endocarditis as the cause for possible mycotic aneurysm, revealed Chronic Rheumatic Valvular Heart Disease, without evidence of vegetations, abscesses, or intracardiac thrombi. This case report seeks to discuss the patient's clinical presentation, CTA findings, and surgical management in a low-resource setting, underscoring the risks of this rare condition if misdiagnosed.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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