Iliac arteriovenous fistula is a rare vascular disease defined as the formation of an abnormal channel between the iliac artery and vein. The high mortality rate associated with an iliac arteriovenous fistula resulting from a ruptured iliac arterial aneurysm necessitates early diagnosis and timely, appropriate management.
We report a case of an 86-year-old man presenting with lower limb pain and edema. Computed tomography angiography demonstrated a large internal iliac artery aneurysm with a fistula to the adjacent vein. Symptoms resolved once a hybrid repair was performed.
{"title":"Hybrid repair of internal iliac arteriovenous aneurysm fistula presenting with lower limb pain: A case report","authors":"Takeshi Uzuka, Akihiko Sasaki, Hitoki Hashiguchi, Hiroki Uchiyama, Ayaka Arihara, Riko Umeta, Kei Mukawa","doi":"10.1016/j.avsurg.2024.100320","DOIUrl":"10.1016/j.avsurg.2024.100320","url":null,"abstract":"<div><p>Iliac arteriovenous fistula is a rare vascular disease defined as the formation of an abnormal channel between the iliac artery and vein. The high mortality rate associated with an iliac arteriovenous fistula resulting from a ruptured iliac arterial aneurysm necessitates early diagnosis and timely, appropriate management.</p><p>We report a case of an 86-year-old man presenting with lower limb pain and edema. Computed tomography angiography demonstrated a large internal iliac artery aneurysm with a fistula to the adjacent vein. Symptoms resolved once a hybrid repair was performed.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100320"},"PeriodicalIF":0.0,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000722/pdfft?md5=3a2ba16d1be277b3747eb38916aa2d19&pid=1-s2.0-S2772687824000722-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141711373","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}
Pub Date : 2024-07-10DOI: 10.1016/j.avsurg.2024.100318
Yuta Tajima, Yoshihisa Tamate, Kentaro Akabane, Shuji Toyama, Tetsuo Watanabe
Objective
There are various techniques for additional placement of Gore Excluder Iliac Branch Endoprosthesis (IBE; W. L. Gore & Associates, Flagstaff, AZ) for common iliac artery aneurysms following endovascular aneurysm repair (EVAR). However, these techniques do not always allow for the placement of approved, dedicated, self-expanding stent grafts (SESGs), such as internal iliac components, for internal iliac artery bridging. Here, we introduce the “U-turn Dryseal sheath technique,” which can successfully place SESGs using only a unilateral femoral approach.
Method
We inserted a modified 16-Fr Gore Dryseal Flex Introducer sheath (Dryseal sheath) and placed an iliac branch component. Then, we inserted a 12-Fr Dryseal sheath (33 cm) into a 16-Fr sheath and created a U-turn shape of the 12-Fr sheath toward the internal iliac artery portion using an ipsilateral U-turn wire. Next, we placed the SESG through the 12-Fr sheath via the shortest route.
Results
We used this technique to perform IBE placement following EVAR in eight cases and successfully placed the SESGs in all cases without any type Ⅰ or Ⅲ endoleaks.
Conclusion
The U-turn Dryseal sheath technique allows the stable additional placement of IBE with approved SESGs for internal iliac artery bridging in selected cases.
目的:在血管内动脉瘤修补术(EVAR)之后,有多种技术可以为髂总动脉瘤额外植入戈尔髂支内支架(IBE;W. L. Gore & Associates, Flagstaff, AZ)。然而,这些技术并不总能将经批准的专用自扩张支架移植物(SESG)(如髂内组件)用于髂内动脉桥接。在此,我们介绍了 "U-turn Dryseal 鞘技术",该技术只需单侧股骨入路即可成功置入 SESG。方法我们插入改良的 16-Fr Gore Dryseal Flex Introducer 鞘(Dryseal 鞘)并置入髂支组件。然后,我们将一个 12 英尺的 Dryseal 鞘(33 厘米)插入 16 英尺的鞘中,并使用同侧 U 形导线将 12 英尺的鞘向髂内动脉部分 U 形翻转。结果我们在 8 个病例中使用该技术进行了 EVAR 后的 IBE 置入,并在所有病例中成功置入了 SESG,且未出现任何Ⅰ型或Ⅲ型内漏。结论U-turn Dryseal 鞘技术允许在选定病例中使用经批准的 SESG 稳定地额外置入 IBE,用于髂内动脉桥接。
{"title":"U-turn Dryseal sheath technique for additional Gore Iliac Branch Endoprosthesis placement","authors":"Yuta Tajima, Yoshihisa Tamate, Kentaro Akabane, Shuji Toyama, Tetsuo Watanabe","doi":"10.1016/j.avsurg.2024.100318","DOIUrl":"10.1016/j.avsurg.2024.100318","url":null,"abstract":"<div><h3>Objective</h3><p>There are various techniques for additional placement of Gore Excluder Iliac Branch Endoprosthesis (IBE; W. L. Gore & Associates, Flagstaff, AZ) for common iliac artery aneurysms following endovascular aneurysm repair (EVAR). However, these techniques do not always allow for the placement of approved, dedicated, self-expanding stent grafts (SESGs), such as internal iliac components, for internal iliac artery bridging. Here, we introduce the “U-turn Dryseal sheath technique,” which can successfully place SESGs using only a unilateral femoral approach.</p></div><div><h3>Method</h3><p>We inserted a modified 16-Fr Gore Dryseal Flex Introducer sheath (Dryseal sheath) and placed an iliac branch component. Then, we inserted a 12-Fr Dryseal sheath (33 cm) into a 16-Fr sheath and created a U-turn shape of the 12-Fr sheath toward the internal iliac artery portion using an ipsilateral U-turn wire. Next, we placed the SESG through the 12-Fr sheath via the shortest route.</p></div><div><h3>Results</h3><p>We used this technique to perform IBE placement following EVAR in eight cases and successfully placed the SESGs in all cases without any type Ⅰ or Ⅲ endoleaks.</p></div><div><h3>Conclusion</h3><p>The U-turn Dryseal sheath technique allows the stable additional placement of IBE with approved SESGs for internal iliac artery bridging in selected cases.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100318"},"PeriodicalIF":0.0,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000709/pdfft?md5=ac67b5d5d5cbd1e8871f2bb1ed8a114e&pid=1-s2.0-S2772687824000709-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141630523","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}
Retrograde open mesenteric stenting (ROMS) is an alternative to mesenteric bypass/antegrade angioplasty and stenting in patients with acute and chronic mesenteric ischemia. We present a case and literature review utilizing ROMS in a patient with severe vascular occlusive disease to treat her superior mesenteric artery (SMA) stenosis.
Case report
A 63-year-old woman with a history of severe vascular occlusive disease and previous extensive surgical interventions required ROMS due to SMA stenosis for acute on chronic mesenteric ischemia. There were no in-hospital complications. We also performed a review of the literature to assess the technical success and clinical outcomes of ROMS.
Results
A total of six articles with 210 patients (92 males, 118 females) were included. In the studies where the celiac artery and SMA were implicated, technical success was 92.9%, conversion to bypass was 4.3%, and 30-day mortality was 29.5%. In the studies where only the SMA was implicated, technical success was 90.7%, conversion to bypass was 7.2%, and 30-day mortality was 23.7%. In cases of acute mesenteric ischemia, the 30-day mortality rate was 34.2%.
Conclusion
Though open surgical bypass and antegrade endovascular angioplasty and stenting have been the first-line treatment options for mesenteric ischemia, ROMS is an excellent alternative option with a high technical success rate that can be utilized when conventional treatment modalities are not technically feasible or in the setting of concomitant open abdominal exploration for the assessment of bowel ischemia.
目的逆行开放式肠系膜支架植入术(ROMS)是肠系膜搭桥术/逆行血管成形术和支架植入术的替代方法,适用于急慢性肠系膜缺血患者。病例报告:一名 63 岁的女性患者患有严重的血管闭塞性疾病,既往曾接受过大量外科手术治疗,因 SMA 狭窄而需要采用 ROMS 手术治疗急性和慢性肠系膜缺血。院内无并发症。我们还对文献进行了回顾,以评估 ROMS 的技术成功率和临床效果。在涉及腹腔动脉和 SMA 的研究中,技术成功率为 92.9%,转为搭桥的比例为 4.3%,30 天死亡率为 29.5%。在仅涉及 SMA 的研究中,技术成功率为 90.7%,转为搭桥的比例为 7.2%,30 天死亡率为 23.7%。结论虽然开放手术搭桥和前向血管内成形术及支架植入术一直是肠系膜缺血的一线治疗方案,但 ROMS 是一种技术成功率高的极佳替代方案,在传统治疗方法技术上不可行或同时进行开腹探查以评估肠缺血的情况下可以使用。
{"title":"Retrograde Open Mesenteric Stenting: A Case Report and Literature Review","authors":"Suren Jeevaratnam , Houssam Farres , Camilo Polania-Sandoval , Yetzali Claudio-Medina , Hennessy Morales-Arroyo , Young Erben","doi":"10.1016/j.avsurg.2024.100319","DOIUrl":"10.1016/j.avsurg.2024.100319","url":null,"abstract":"<div><h3>Objective</h3><p>Retrograde open mesenteric stenting (ROMS) is an alternative to mesenteric bypass/antegrade angioplasty and stenting in patients with acute and chronic mesenteric ischemia. We present a case and literature review utilizing ROMS in a patient with severe vascular occlusive disease to treat her superior mesenteric artery (SMA) stenosis.</p></div><div><h3>Case report</h3><p>A 63-year-old woman with a history of severe vascular occlusive disease and previous extensive surgical interventions required ROMS due to SMA stenosis for acute on chronic mesenteric ischemia. There were no in-hospital complications. We also performed a review of the literature to assess the technical success and clinical outcomes of ROMS.</p></div><div><h3>Results</h3><p>A total of six articles with 210 patients (92 males, 118 females) were included. In the studies where the celiac artery and SMA were implicated, technical success was 92.9%, conversion to bypass was 4.3%, and 30-day mortality was 29.5%. In the studies where only the SMA was implicated, technical success was 90.7%, conversion to bypass was 7.2%, and 30-day mortality was 23.7%. In cases of acute mesenteric ischemia, the 30-day mortality rate was 34.2%.</p></div><div><h3>Conclusion</h3><p>Though open surgical bypass and antegrade endovascular angioplasty and stenting have been the first-line treatment options for mesenteric ischemia, ROMS is an excellent alternative option with a high technical success rate that can be utilized when conventional treatment modalities are not technically feasible or in the setting of concomitant open abdominal exploration for the assessment of bowel ischemia.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100319"},"PeriodicalIF":0.0,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000710/pdfft?md5=9d7e82bc89ccce300b06fad204b1d303&pid=1-s2.0-S2772687824000710-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141711092","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}
Pub Date : 2024-07-09DOI: 10.1016/j.avsurg.2024.100317
Nicola Habash , Gaurang Joshi , Mohammed Ali , Michael Nooromid , Babak Abai
Successful thoracic endovascular aortic repair (TEVAR) for type B aortic dissections (TBAD) relies on securing the stentgraft's distal landing zone to prevent retrograde flow and false lumen pressurization. We describe a 60-year-old male with a TBAD undergoing TEVAR with electrocautery-wire fenestration of the dissection septum, providing a controlled method to enhance the distal landing zone for graft placement. Postoperatively, the patient experienced spinal cord ischemia, resolving with the placement of a lumbar drain and increasing mean arterial pressures. Follow-up imaging demonstrated a well-sealed repair without endoleaks. This case highlights the importance of surgical technique selection and postoperative monitoring for complications.
B 型主动脉夹层 (TBAD) 的胸腔内血管主动脉修复术 (TEVAR) 成功与否取决于支架移植物远端着陆区的安全性,以防止逆流和假腔压。我们描述了一名 60 岁男性主动脉夹层患者接受 TEVAR 手术的情况,该手术采用电烧-钢丝对夹层隔膜进行开孔,提供了一种可控方法来增强支架远端着陆区,以便放置移植物。术后,患者出现脊髓缺血,在放置腰椎引流管和增加平均动脉压后缓解。随访造影显示,修复处密封良好,没有内漏。该病例强调了手术技术选择和术后并发症监测的重要性。
{"title":"Electrocautery wire fenestration prior to thoracic endovascular aortic repair to optimize the distal landing zone in thoracic aortic dissections","authors":"Nicola Habash , Gaurang Joshi , Mohammed Ali , Michael Nooromid , Babak Abai","doi":"10.1016/j.avsurg.2024.100317","DOIUrl":"10.1016/j.avsurg.2024.100317","url":null,"abstract":"<div><p>Successful thoracic endovascular aortic repair (TEVAR) for type B aortic dissections (TBAD) relies on securing the stentgraft's distal landing zone to prevent retrograde flow and false lumen pressurization. We describe a 60-year-old male with a TBAD undergoing TEVAR with electrocautery-wire fenestration of the dissection septum, providing a controlled method to enhance the distal landing zone for graft placement. Postoperatively, the patient experienced spinal cord ischemia, resolving with the placement of a lumbar drain and increasing mean arterial pressures. Follow-up imaging demonstrated a well-sealed repair without endoleaks. This case highlights the importance of surgical technique selection and postoperative monitoring for complications.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100317"},"PeriodicalIF":0.0,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000692/pdfft?md5=167143809e22cba3622dc7acb23ec7d5&pid=1-s2.0-S2772687824000692-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141630362","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}
Pub Date : 2024-07-08DOI: 10.1016/j.avsurg.2024.100315
Dorcie Ann Gillette , Albert Pedroza , Maen Aboul Hosn
Thoracic outlet syndrome (TOS) is a rare condition that results from compression of the neurovascular structures as they pass through the thoracic outlet. In this case series, we report on three patients who developed TOS following the creation of an upper extremity arteriovenous fistula (AVF). Patients were successfully treated with first rib resection and pec minor release with venoplasty and neurolysis as indicated. Surgical intervention improved symptoms and preserved dialysis access function in all patients. Thus, with the right constellation of symptoms, clinicians should consider TOS as a differential in patients following AVF creation.
胸廓出口综合征(TOS)是一种罕见的疾病,是由于神经血管结构在通过胸廓出口时受到挤压所致。在本病例系列中,我们报告了三名患者在上肢动静脉瘘(AVF)形成后出现 TOS 的病例。患者成功接受了第一肋骨切除术和胸小肌松解术,并根据情况进行了静脉成形术和神经切除术。手术干预改善了所有患者的症状,并保留了透析通路的功能。因此,临床医生应将TOS作为动静脉瘘形成后患者的一个鉴别因素,并考虑适当的症状组合。
{"title":"Thoracic outlet syndrome in dialysis patients: A case series and review","authors":"Dorcie Ann Gillette , Albert Pedroza , Maen Aboul Hosn","doi":"10.1016/j.avsurg.2024.100315","DOIUrl":"https://doi.org/10.1016/j.avsurg.2024.100315","url":null,"abstract":"<div><p>Thoracic outlet syndrome (TOS) is a rare condition that results from compression of the neurovascular structures as they pass through the thoracic outlet. In this case series, we report on three patients who developed TOS following the creation of an upper extremity arteriovenous fistula (AVF). Patients were successfully treated with first rib resection and pec minor release with venoplasty and neurolysis as indicated. Surgical intervention improved symptoms and preserved dialysis access function in all patients. Thus, with the right constellation of symptoms, clinicians should consider TOS as a differential in patients following AVF creation.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100315"},"PeriodicalIF":0.0,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000679/pdfft?md5=fc5cf41b7008cad3965f974d61d436c3&pid=1-s2.0-S2772687824000679-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141607091","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}
Pub Date : 2024-07-06DOI: 10.1016/j.avsurg.2024.100311
Margarita I Pipinos , Elizabeth A Amato-Hanner , Aaron M Murray , Shalmali Mirajkar , Jennifer L Gamache , Safina Hafeez , Tanya M Wildes , Jason N MacTaggart
A 52-year-old woman presented with acute digital ischemia and pain in all five digits of her right hand. Upper extremity arterial duplex demonstrated normal flow to the wrist, but upper extremity Computed Tomography Angiography (CTA) demonstrated an atretic appearing brachial artery at the mid-humerus, variant superficial ulnar artery, and a radial artery that truncated at the wrist. The patient was diagnosed with digital ischemia secondary to polycythemia and was started on intravenous anticoagulation. Her symptoms improved and she was converted to oral anti-coagulation and anti-platelet therapy supplemented by weekly therapeutic phlebotomy. The patient's condition improved at 1-month follow up, as indicated by laboratory, imaging, and symptoms. In this case report, we detail the presentation and management of upper extremity ischemia in the setting of polycythemia in a patient with small, tortuous, and aberrant vasculature.
{"title":"Blood letting as an ancient cure for an unusual manifestation of polycythemia","authors":"Margarita I Pipinos , Elizabeth A Amato-Hanner , Aaron M Murray , Shalmali Mirajkar , Jennifer L Gamache , Safina Hafeez , Tanya M Wildes , Jason N MacTaggart","doi":"10.1016/j.avsurg.2024.100311","DOIUrl":"https://doi.org/10.1016/j.avsurg.2024.100311","url":null,"abstract":"<div><p>A 52-year-old woman presented with acute digital ischemia and pain in all five digits of her right hand. Upper extremity arterial duplex demonstrated normal flow to the wrist, but upper extremity Computed Tomography Angiography (CTA) demonstrated an atretic appearing brachial artery at the mid-humerus, variant superficial ulnar artery, and a radial artery that truncated at the wrist. The patient was diagnosed with digital ischemia secondary to polycythemia and was started on intravenous anticoagulation. Her symptoms improved and she was converted to oral anti-coagulation and anti-platelet therapy supplemented by weekly therapeutic phlebotomy. The patient's condition improved at 1-month follow up, as indicated by laboratory, imaging, and symptoms. In this case report, we detail the presentation and management of upper extremity ischemia in the setting of polycythemia in a patient with small, tortuous, and aberrant vasculature.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100311"},"PeriodicalIF":0.0,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000631/pdfft?md5=a4a802006fe5ae917749ee8bc2092f18&pid=1-s2.0-S2772687824000631-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141593814","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}
Pub Date : 2024-07-03DOI: 10.1016/j.avsurg.2024.100314
Audrey Horn , Kelli L. Summers , William Fuell , Adarsh Vijay , Hoonbae Jeon , Melissa Donovan , Kiara Tulla , Anil Paramesh
A 63-year-old male developed a mycotic pseudoaneurysm (MPA) two months after a renal transplant at the anastomotic site. He presented with uncontrolled hypertension and elevated creatinine. The pseudoaneurysm occurred at the anastomosis between the two donor renal arteries and the left external iliac artery. We describe a unique surgical reconstruction where the MPA was resected and the vasculature was reconstructed using deceased donor vessels. A deceased donor common iliac artery including superior gluteal and inferior gluteal branches were used as a jump graft from the contralateral common iliac artery to the two transplanted renal arteries. The external iliac artery was repaired with an interposition bypass using deceased donor iliac vein. The patient received 8 weeks of antifungal therapy after the specimen grew candida albicans. Post-operatively, the patient had an acute kidney injury requiring dialysis, but after two months of dialysis, his renal function returned to normal and he remains dialysis-free.
{"title":"Salvage of a kidney transplant with a mycotic extrarenal pseudoaneursym using donor vessels","authors":"Audrey Horn , Kelli L. Summers , William Fuell , Adarsh Vijay , Hoonbae Jeon , Melissa Donovan , Kiara Tulla , Anil Paramesh","doi":"10.1016/j.avsurg.2024.100314","DOIUrl":"https://doi.org/10.1016/j.avsurg.2024.100314","url":null,"abstract":"<div><p>A 63-year-old male developed a mycotic pseudoaneurysm (MPA) two months after a renal transplant at the anastomotic site. He presented with uncontrolled hypertension and elevated creatinine. The pseudoaneurysm occurred at the anastomosis between the two donor renal arteries and the left external iliac artery. We describe a unique surgical reconstruction where the MPA was resected and the vasculature was reconstructed using deceased donor vessels. A deceased donor common iliac artery including superior gluteal and inferior gluteal branches were used as a jump graft from the contralateral common iliac artery to the two transplanted renal arteries. The external iliac artery was repaired with an interposition bypass using deceased donor iliac vein. The patient received 8 weeks of antifungal therapy after the specimen grew candida albicans. Post-operatively, the patient had an acute kidney injury requiring dialysis, but after two months of dialysis, his renal function returned to normal and he remains dialysis-free.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100314"},"PeriodicalIF":0.0,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000667/pdfft?md5=e44344ce88ee20dfe204028dcc376f19&pid=1-s2.0-S2772687824000667-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141582296","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}
Pub Date : 2024-07-02DOI: 10.1016/j.avsurg.2024.100313
Christine A. Parks , Winsor P. Chen , Christopher G. Gomez , Nicos Labropoulos , George Koullias , Scott S. Berman , Luis R. Leon Jr.
In the past four decades, reports of an unusual vascular disease affecting young and otherwise healthy endurance athletes have begun to emerge. This rare entity has been coined as external iliac artery endofibrosis (EIAE). It has been primarily described in high-level competitive cyclists, suggesting a biomechanical etiology given the repetitive flexion and extension of the hip joint associated with cycling.1,2 Patients present with symptoms of claudication at peak levels of exertion, levels not usually achievable by the untrained individual. Lesions are predominantly isolated to the external iliac artery (EIA), and histologic examination reveals endothelial thickening and fibrosis without evidence of atherosclerosis.1–5 Cases of EIAE have been overwhelmingly described in male athletes, with a paucity of reports in females.2,3 We herein describe two cases of elite female athletes afflicted by EIAE and review the current literature pertaining to this entity in females. Both patients consented to publication of their case details and images.
{"title":"External iliac artery endofibrosis in females: Case reports and review of the literature","authors":"Christine A. Parks , Winsor P. Chen , Christopher G. Gomez , Nicos Labropoulos , George Koullias , Scott S. Berman , Luis R. Leon Jr.","doi":"10.1016/j.avsurg.2024.100313","DOIUrl":"10.1016/j.avsurg.2024.100313","url":null,"abstract":"<div><p>In the past four decades, reports of an unusual vascular disease affecting young and otherwise healthy endurance athletes have begun to emerge. This rare entity has been coined as external iliac artery endofibrosis (EIAE). It has been primarily described in high-level competitive cyclists, suggesting a biomechanical etiology given the repetitive flexion and extension of the hip joint associated with cycling.<sup>1,2</sup> Patients present with symptoms of claudication at peak levels of exertion, levels not usually achievable by the untrained individual. Lesions are predominantly isolated to the external iliac artery (EIA), and histologic examination reveals endothelial thickening and fibrosis without evidence of atherosclerosis.<sup>1–5</sup> Cases of EIAE have been overwhelmingly described in male athletes, with a paucity of reports in females.<sup>2,3</sup> We herein describe two cases of elite female athletes afflicted by EIAE and review the current literature pertaining to this entity in females. Both patients consented to publication of their case details and images.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100313"},"PeriodicalIF":0.0,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000655/pdfft?md5=3e9e59f5b8901dc50b1937fcfcda093f&pid=1-s2.0-S2772687824000655-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141699418","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}
Pub Date : 2024-07-02DOI: 10.1016/j.avsurg.2024.100312
Alphonse NZOMVUAMA , Jean-Jacques KALONGO , Blondel BAYENEKENE , Stéphane YANDA , M. Jacques NSUAMI
The infectious pseudoaneurysm of the common carotid artery is a rare observation in children. We present a case of ruptured infectious common carotid aneurysm in a 14-year-old girl managed in the Democratic Republic of Congo. We performed an arterial reconstruction with a saphenous vein patch. Post-operative course was simple. The patient was discharged from the hospital at post-operative day 15. She was doing well and had returned to school. Rupture of an infectious pseudoaneurysm of the common carotid artery constitutes a serious, life-threatening accident. As we have shown in this case report, its management with successful results is indeed possible, even in a resource-limited environment.
{"title":"Ruptured infectious pseudoaneurysm of the common carotid artery in a 14-year-old girl. management in the DR Congo","authors":"Alphonse NZOMVUAMA , Jean-Jacques KALONGO , Blondel BAYENEKENE , Stéphane YANDA , M. Jacques NSUAMI","doi":"10.1016/j.avsurg.2024.100312","DOIUrl":"https://doi.org/10.1016/j.avsurg.2024.100312","url":null,"abstract":"<div><p>The infectious pseudoaneurysm of the common carotid artery is a rare observation in children. We present a case of ruptured infectious common carotid aneurysm in a 14-year-old girl managed in the Democratic Republic of Congo. We performed an arterial reconstruction with a saphenous vein patch. Post-operative course was simple. The patient was discharged from the hospital at post-operative day 15. She was doing well and had returned to school. Rupture of an infectious pseudoaneurysm of the common carotid artery constitutes a serious, life-threatening accident. As we have shown in this case report, its management with successful results is indeed possible, even in a resource-limited environment.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100312"},"PeriodicalIF":0.0,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772687824000643/pdfft?md5=1fb0098332760d3108e220b97201681c&pid=1-s2.0-S2772687824000643-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141582294","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}
Pub Date : 2024-06-29DOI: 10.1016/j.avsurg.2024.100310
Camilo Polania Sandoval, Houssam Farres, Yaman Alsabbagh, Young Erben
Introduction
Peripheral artery disease (PAD) affects over 200 million people globally. A small subset of PAD patients are a result of radiation-induced peripheral artery disease (RIPAD). Radiation changes affect vascular physiology and cause arteriopathy with vessel damage and subsequent occlusion. This report details a case of common femoral and superficial femoral artery RIPAD with a review of the existing literature.
Case report
A 40-year-old male patient presented with a six-month history of left leg rest pain. He had 30 years prior synovial cell sarcoma of the thigh treated with chemo- and radiation therapy with chronic residual lymphedema managed with compression therapy. Preoperative non-invasive studies demonstrated an ankle-brachial index of 0.42. Computed tomography angiography of the leg demonstrated a small caliber external iliac artery and occlusion of the common femoral and superficial femoral arteries. A left external iliac to above-the-knee popliteal artery bypass using a contralateral great saphenous vein was performed. Six weeks after operative intervention, the groin wound broke down and became infected. He required emergent repair of this bypass using 4 cm cryopreserved vein interposition graft. Intraoperative cultures were positive for Staphylococcus epidermidis and Finegoldia magna. At a 4.5-year follow-up, the patient remains active with a patent bypass and continues to manage his leg lymphedema with thigh-high elastic compression stockings.
Conclusion
Clinical expertise is required to detect RIPAD early on. There is a high risk for post-operative complications due to radiation damage to surrounding tissues. Open surgical repair is the preferred treatment strategy. Lymphedema and wound healing complications are key to managing patients affected by RIPAD.
{"title":"Chronic limb threatening ischemia due to radiation-induced arteriopathy 30 years after soft tissue sarcoma resection and radiation therapy: Case report and review of the literature","authors":"Camilo Polania Sandoval, Houssam Farres, Yaman Alsabbagh, Young Erben","doi":"10.1016/j.avsurg.2024.100310","DOIUrl":"https://doi.org/10.1016/j.avsurg.2024.100310","url":null,"abstract":"<div><h3>Introduction</h3><p>Peripheral artery disease (PAD) affects over 200 million people globally. A small subset of PAD patients are a result of radiation-induced peripheral artery disease (RIPAD). Radiation changes affect vascular physiology and cause arteriopathy with vessel damage and subsequent occlusion. This report details a case of common femoral and superficial femoral artery RIPAD with a review of the existing literature.</p></div><div><h3>Case report</h3><p>A 40-year-old male patient presented with a six-month history of left leg rest pain. He had 30 years prior synovial cell sarcoma of the thigh treated with chemo- and radiation therapy with chronic residual lymphedema managed with compression therapy. Preoperative non-invasive studies demonstrated an ankle-brachial index of 0.42. Computed tomography angiography of the leg demonstrated a small caliber external iliac artery and occlusion of the common femoral and superficial femoral arteries. A left external iliac to above-the-knee popliteal artery bypass using a contralateral great saphenous vein was performed. Six weeks after operative intervention, the groin wound broke down and became infected. He required emergent repair of this bypass using 4 cm cryopreserved vein interposition graft. Intraoperative cultures were positive for Staphylococcus epidermidis and Finegoldia magna. At a 4.5-year follow-up, the patient remains active with a patent bypass and continues to manage his leg lymphedema with thigh-high elastic compression stockings.</p></div><div><h3>Conclusion</h3><p>Clinical expertise is required to detect RIPAD early on. There is a high risk for post-operative complications due to radiation damage to surrounding tissues. Open surgical repair is the preferred treatment strategy. Lymphedema and wound healing complications are key to managing patients affected by RIPAD.</p></div>","PeriodicalId":72235,"journal":{"name":"Annals of vascular surgery. Brief reports and innovations","volume":"4 3","pages":"Article 100310"},"PeriodicalIF":0.0,"publicationDate":"2024-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S277268782400062X/pdfft?md5=3122f4650bd7a99d89387a75536c07a3&pid=1-s2.0-S277268782400062X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141582295","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}