Annals of vascular surgery. Brief reports and innovations最新文献_第3页

Traumatic common carotid artery-internal jugular vein fistula in an acute setting: A case report with review of literature 外伤性颈总动脉-颈内静脉急性瘘：1例报告并文献复习

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-04-12 DOI: 10.1016/j.avsurg.2025.100377

Ezaz Ahmed , Aamir Mohammad , Saifullah Khalid , Syed Shamayal Rabbani , Mohd Azam Haseen , Areeba Khursheed

{"title":"Traumatic common carotid artery-internal jugular vein fistula in an acute setting: A case report with review of literature","authors":"Ezaz Ahmed , Aamir Mohammad , Saifullah Khalid , Syed Shamayal Rabbani , Mohd Azam Haseen , Areeba Khursheed","doi":"10.1016/j.avsurg.2025.100377","DOIUrl":"10.1016/j.avsurg.2025.100377","url":null,"abstract":"<div><h3>Introduction</h3><div>Arteriovenous fistulas may be due to trauma or due to iatrogenic causes. These patients present with non specific symptoms such as high output heart failure years later after the development of the fistula. Formation of the fistula in an acute setting immediately after the trauma is a rare occurrence. Here we present a case of a 19 year old boy who presented with a fistula a few hours after the trauma.</div></div><div><h3>Case Summary</h3><div>A 19 year old boy with history of firearm injury to the left side of the neck presented with a palpable thrill and an audible bruit over the site of injury. CT Angiography was done which showed multiple pseudo aneurysms arising from the left common carotid artery(CCA) and a communication with the adjacent internal jugular vein(IJV). Endovascular embolisation of the fistula was done and a stent was placed across the fistula. On check angiography, no fistulous communication was noted between the left CCA and IJV post procedure and the patient was discharged under stable conditions.</div></div><div><h3>Conclusion</h3><div>Traumatic AVFs involving the common carotid artery and internal jugular veins is not uncommon but usually presents after a period of time with added morbidity, and has been not been reported frequently. Also, the fistulas present much later unlike in this case report which presented very early. Ultrasound or CT angiogram may aid in diagnosis. However, conventional angiogram is the gold standard for diagnosis with interventional techniques available for managing these high flow fistulas with a good technical success and acceptable safety profile.</div></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"5 2","pages":"Article 100377"},"PeriodicalIF":0.0,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143859836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

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Aortic endograft infection with Mycobacterium bovis following intravesical BCG immunotherapy diagnosed via the Karius Test™- case report and review of literature 经Karius Test™诊断的经膀胱卡介苗免疫治疗后的主动脉内移植物感染牛分枝杆菌-病例报告和文献回顾

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-03-29 DOI: 10.1016/j.avsurg.2025.100376

Prateek Sharma , Kristin Schafer , Richard J. Hankins , Jonathan R. Thompson , Jason R. Cook

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Recurrent rupture of an infected femoral artery pseudoaneurysm secondary to a 35-year-old plated arthrodesis: A case report 继发于 35 岁钢板关节固定术的感染性股动脉假动脉瘤复发破裂：病例报告

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-03-27 DOI: 10.1016/j.avsurg.2025.100375

Dan Y. Draytsel , Deena B. Chihade , Michael J. Costanza , Anthony Feghali

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Internal carotid artery hypoplasia: A case report 颈内动脉发育不全1例

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-03-01 DOI: 10.1016/j.avsurg.2025.100374

Felipe Labaki Pavarino , Adriano Carvalho Guimarães , Halison Vilacorta Araujo de Sousa , Fernanda Fagundes Ribeiro , Zeferino Demartini Junior , Laura Ziemba Araujo , Ricardo Herkenhoff Moreira , Walter Junior Boim de Araujo

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Successful staged treatment of rapidly expanded thoracic aortic aneurysm following abdominal aortic aneurysm occlusion 腹主动脉瘤闭塞后快速扩张胸主动脉瘤的成功分期治疗

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-03-01 DOI: 10.1016/j.avsurg.2025.100372

Shigeshi Ono, Yutaka Takigawa, Hirotoshi Hasegawa

{"title":"Successful staged treatment of rapidly expanded thoracic aortic aneurysm following abdominal aortic aneurysm occlusion","authors":"Shigeshi Ono, Yutaka Takigawa, Hirotoshi Hasegawa","doi":"10.1016/j.avsurg.2025.100372","DOIUrl":"10.1016/j.avsurg.2025.100372","url":null,"abstract":"<div><div>We present the case of a 66-year-old man with aortoiliac occlusive disease (AIOD) complicated by mild abdominal aortic dilation and a thoracic aortic aneurysm (TAA). The patient first presented with intermittent claudication; imaging revealed bilateral common iliac artery stenosis with severe calcification and a dilated thoracic and abdominal aorta. The patient declined treatment and he was lost to follow-up for over two years. Upon returning to the hospital with worsening symptoms, imaging revealed aorto-bilateral iliac occlusion and significant progression of both thoracic and abdominal aortic dilation. Surgical intervention was again declined, and conservative management was continued. Three and a half years after the initial visit, the patient consented to a two-stage treatment. The first stage involved aorto-bifemoral bypass for the AIOD, which improved circulation and relieved symptoms. The second stage, performed three months later, involved thoracic endovascular aortic repair for the TAA. Both procedures were completed without complications, and the patient was discharged in stable condition. This case provides valuable insight into the progression of occlusive arteriosclerosis and aneurysms under conservative observation, highlighting the need for tailored, patient-centric approaches in vascular disease management.</div></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"5 1","pages":"Article 100372"},"PeriodicalIF":0.0,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143550464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Ruptured abdominal aortic aneurysm treated using infrarenal-occlusion-balloon technique with ENDURANT IIs ENDURANTⅱ治疗腹主动脉瘤破裂

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-03-01 DOI: 10.1016/j.avsurg.2025.100373

Shuhei Azuma, Yuki Asada, Ryo Shimada, Shigeru Nakamura

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Catheter-directed aspiration thrombectomy of the IVC/renal vein for acute renal vein thrombosis in a patient with nephrotic syndrome: A Case Report 导管引导下静脉/肾静脉吸血栓切除术治疗肾病综合征患者急性肾静脉血栓：1例报告

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-02-18 DOI: 10.1016/j.avsurg.2025.100371

Neil K. Jain , Hernoor Athwal , Michael Abramson

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Intravascular lipoma with extravascular extension, a rare phenomena and review of the literature 血管内脂肪瘤伴血管外延伸，罕见现象及文献回顾

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-02-17 DOI: 10.1016/j.avsurg.2025.100370

Mennatalla Hegazi , Charlene Yuan , Nii-Kabu Kabutey , Roy M Fujitani , Hari Keshava , Ali Mahtabifard , Anthony H Chau

{"title":"Intravascular lipoma with extravascular extension, a rare phenomena and review of the literature","authors":"Mennatalla Hegazi , Charlene Yuan , Nii-Kabu Kabutey , Roy M Fujitani , Hari Keshava , Ali Mahtabifard , Anthony H Chau","doi":"10.1016/j.avsurg.2025.100370","DOIUrl":"10.1016/j.avsurg.2025.100370","url":null,"abstract":"<div><div>Lipomas are the most common soft tissue tumors, accounting for half of all soft tissue masses. However, intravascular lipomas (IVLs) are rare. IVLs have been described in case reports in the various major veins. They are often asymptomatic and found incidentally. Given the risk of malignancy, as liposarcomas are the second most common soft tissue sarcoma in adults and account for 1 % of all malignancies, histological differentiation is important, and surgical excision remains the mainstay of treatment in the literature. We present the case of a 61-year-old male who presented with left chest pain that radiated to his left shoulder and arm. On further evaluation, the patient endorsed left-hand swelling and weakness and increased prominence of veins in the left upper extremity. He underwent a CT scan that showed a hypodense mass with fat attenuation in the left innominate vein extending extra-vascularly and into the left internal jugular vein, measuring 2.3 × 2.0 × 5.2 cm. Successful surgical excision and reconstruction of the innominate vein with reimplantation of the left internal jugular vein was performed through median sternotomy and left cervical incision. The postoperative course was unremarkable, and the patient recovered well. The clinical presentation of an intravascular lipoma in a large caliber vessel can be subtle and nonspecific. This case report characterizes this rare vascular tumor and includes a contemporary literature review, summarizing the diagnosis and treatment options.</div></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"5 1","pages":"Article 100370"},"PeriodicalIF":0.0,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143453840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Paget-Schroetter Syndrome secondary to anomalous right-sided aortic arch: A case report 右主动脉弓异常继发的Paget-Schroetter综合征1例报告

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-02-09 DOI: 10.1016/j.avsurg.2025.100368

Katrina Pardo , Sofia Steger , Edgar Galinanes , Juan Carlos Pereda

{"title":"Paget-Schroetter Syndrome secondary to anomalous right-sided aortic arch: A case report","authors":"Katrina Pardo , Sofia Steger , Edgar Galinanes , Juan Carlos Pereda","doi":"10.1016/j.avsurg.2025.100368","DOIUrl":"10.1016/j.avsurg.2025.100368","url":null,"abstract":"<div><div>Thoracic Outlet Syndrome (TOS) is a rare condition, with an estimated prevalence of about 3 in 100,000 individuals.<sup>1</sup> Venogenic TOS, also referred to as Paget-Schroetter Syndrome (PSS), is rarer than neurogenic TOS with an estimated prevalence of 1 in 100,000.<sup>1</sup> In this case report, we present a rare case of PSS secondary to an anomalous right-sided aortic arch with branching anomalies, which are described poorly in the literature. The patient, a 41-year-old male with no significant past medical history, presented with classic PSS symptoms that include left neck swelling and pain, intermittent numbness, and swelling in the left arm. Following admission, a chest CT with contrast revealed a right-sided aortic arch along with a left common carotid artery and left subclavian artery that share a common trunk. Ultrasound revealed thrombosis of the left subclavian and innominate veins consistent with PSS. He underwent an aspiration thrombectomy and catheter-directed thrombolytic therapy. The patient is currently symptom-free and successfully managed in the short term with anticoagulation therapy.</div></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"5 1","pages":"Article 100368"},"PeriodicalIF":0.0,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143395651","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

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Facial flushing can be a rare presentation of SVC syndrome 面部潮红是SVC综合征的罕见表现

Annals of vascular surgery. Brief reports and innovations Pub Date : 2025-02-09 DOI: 10.1016/j.avsurg.2025.100369

Claire Elizabeth Cassianni , Noora Jabeen , Tiziano Tallarita , Michel K Barsoum , Vaibhav R. Vaidya , Indrani Sen

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