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一名年轻男性的自发性孤立性髂动脉夹层:病例报告及文献复习

Spontaneous isolated iliac artery dissection in a young male: Case report and review of literature.

作者信息

Tambe Rahul, Patil Sushant, Gohil Krutika, Parikh Rashmi, Nadeem Arsalan, Wanjari Mayur, Mittal Gaurav

机构信息

DNB Internal Medicine, Department of Internal Medicine, Nanavati Max Super Specialty Hospital, Mumbai, Maharashtra, India.

DNB Cardiology, Department of Cardiology, Nanavati Max Super Specialty Hospital, Mumbai, Maharashtra, India.

出版信息

Radiol Case Rep. 2024 Sep 10;19(12):5682-5687. doi: 10.1016/j.radcr.2024.08.064. eCollection 2024 Dec.

Abstract

Spontaneous isolated dissection of the iliac artery (SID-IA) is a rare vascular condition typically associated with trauma or connective tissue disorders. We present a unique case of a 39-year-old male without known risk factors or trauma history who presented with lower abdominal pain. Diagnostic imaging revealed SID-IA involving the right external iliac artery with thrombus formation. Despite negative findings for connective tissue disorders, the patient underwent successful endovascular stenting following initial medical management. Vigilance in diagnosis and prompt intervention are crucial in managing SID-IA to prevent complications such as limb ischemia and aneurysm formation. This case emphasizes the importance of considering SID-IA in young patients presenting with abdominal pain, even in the absence of traditional risk factors, and highlights evolving treatment options for this rare condition.

摘要

自发性孤立性髂动脉夹层(SID-IA)是一种罕见的血管疾病,通常与创伤或结缔组织疾病有关。我们报告了一例独特的病例,一名39岁男性,无已知危险因素或创伤史,出现下腹部疼痛。诊断性影像学检查显示SID-IA累及右髂外动脉并形成血栓。尽管结缔组织疾病检查结果为阴性,但患者在初始药物治疗后成功接受了血管内支架置入术。在管理SID-IA时,保持诊断警惕性并及时干预对于预防肢体缺血和动脉瘤形成等并发症至关重要。该病例强调了在无传统危险因素的腹痛年轻患者中考虑SID-IA的重要性,并突出了这种罕见疾病不断发展的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d743/11415835/d821bb8954dd/gr1.jpg

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