Case Reports in Vascular Medicine最新文献

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Bilateral Hypothenar Hammer Syndrome Case Presentation and Literature Review. 双侧鱼际下锤综合征病例报告及文献复习。
Case Reports in Vascular Medicine Pub Date : 2022-06-28 eCollection Date: 2022-01-01 DOI: 10.1155/2022/2078772
Andrés-Trasahedo Estíbaliz, Labrador-Sánchez Eztizen, Salazar-Asencio Osman-Alberto, Flores-Robles Bryan-Josué, Pinillos-Aransay Valvanera, Laura Torrecilla Lerena, López-Martín Juan-Antonio
{"title":"Bilateral Hypothenar Hammer Syndrome Case Presentation and Literature Review.","authors":"Andrés-Trasahedo Estíbaliz,&nbsp;Labrador-Sánchez Eztizen,&nbsp;Salazar-Asencio Osman-Alberto,&nbsp;Flores-Robles Bryan-Josué,&nbsp;Pinillos-Aransay Valvanera,&nbsp;Laura Torrecilla Lerena,&nbsp;López-Martín Juan-Antonio","doi":"10.1155/2022/2078772","DOIUrl":"https://doi.org/10.1155/2022/2078772","url":null,"abstract":"<p><p>Hypothenar hammer syndrome is a rare cause of vascular insufficiency. Generally, patients report a history of repetitive trauma to the hypothenar region of the hand. Symptoms often consist of cold intolerance, pain, paleness, and paresthesia due to digital ischemia. The severity of these symptoms will depend on the extent of ulnar artery occlusion and the presence or absence of collaterals between this artery's superficial and deep branches. It is a rare clinical entity, which on multiple occasions requires a surgical approach. We present a 63-year-old man with bilateral Raynaud's phenomenon secondary to hypothenar hammer syndrome successfully treated by vascular repair surgery. In patients with Raynaud's phenomenon, it is important to know that there are reversible causes such as hypothenar hammer syndrome.</p>","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":" ","pages":"2078772"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256417/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40580384","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
Iatrogenic Femoral Arteriovenous Fistula with Pseudoaneurysm Associated with Worsening Heart Failure Years after Percutaneous Impella Placement. 医源性股动静脉瘘伴假性动脉瘤与经皮穿刺植入后心衰恶化相关。
Case Reports in Vascular Medicine Pub Date : 2022-06-24 eCollection Date: 2022-01-01 DOI: 10.1155/2022/7005236
Andy Y Wang, Ali Al Jabri, Edward R Jewell, Angela L Jellison
{"title":"Iatrogenic Femoral Arteriovenous Fistula with Pseudoaneurysm Associated with Worsening Heart Failure Years after Percutaneous Impella Placement.","authors":"Andy Y Wang, Ali Al Jabri, Edward R Jewell, Angela L Jellison","doi":"10.1155/2022/7005236","DOIUrl":"10.1155/2022/7005236","url":null,"abstract":"<p><p>Iatrogenic arteriovenous fistulas (AVFs) and pseudoaneurysms (PSAs) are rare complications that may develop years after vascular access, and high-volume flow through these AVFs have been hypothesized to contribute to chronic heart failure. Formation of an AVF or PSA following Impella placement has rarely been described in the literature. Here, we describe a patient who had percutaneous placement of an Impella ventricular assist device through his right groin three years prior, now presenting with worsening heart failure and symptoms of volume overload. He was discovered to have a new, high-flow common femoral artery to femoral vein AVF with an associated PSA. The AVF and associated PSA were resected and repaired. This case study highlights a rare access-site complication from percutaneous Impella placement associated with worsening heart failure, strategies for preventing this complication during peripheral access, and the need to consider this differential in such a patient with a history of peripheral access who has an unexplained worsening of heart failure.</p>","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":" ","pages":"7005236"},"PeriodicalIF":0.0,"publicationDate":"2022-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249528/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40465960","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: 1
Laparoscopic Release for Median Arcuate Ligament Compression Syndrome Associated with a Celiac-Mesenteric Trunk 腹腔-肠系膜干合并正中弓状韧带压迫综合征的腹腔镜松解术
Case Reports in Vascular Medicine Pub Date : 2022-04-22 DOI: 10.1155/2022/3595603
S. Cawich, D. Harnanan, L. Pran
{"title":"Laparoscopic Release for Median Arcuate Ligament Compression Syndrome Associated with a Celiac-Mesenteric Trunk","authors":"S. Cawich, D. Harnanan, L. Pran","doi":"10.1155/2022/3595603","DOIUrl":"https://doi.org/10.1155/2022/3595603","url":null,"abstract":"The median arcuate ligament compression syndrome is a rare entity that occurs in 2 per 100,000 unselected individuals. We present a case where the median arcuate ligament compression syndrome was associated with an equally uncommon anatomic variation—a celiac-mesenteric trunk, which occurs in 0.42-2.7% of unselected individuals. We could find no prior report of a celiac-mesenteric trunk being associated with the median arcuate ligament compression syndrome. This report also adds to the literature to show that a laparoscopic approach to median arcuate ligament release is feasible.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80131450","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}
引用次数: 0
Iatrogenic Fistula in Hemodialysis Patients: An Alternative Approach to Thrombectomy of Arteriovenous Graft (AVG) Thrombosis 血液透析患者的医源性瘘:动静脉移植物(AVG)血栓切除术的另一种方法
Case Reports in Vascular Medicine Pub Date : 2022-04-16 DOI: 10.1155/2022/2417980
R. Dukkipati, A. Benjo, A. Jimenez, I. Lukitsch, Gift Echefu, D. Kumbala
{"title":"Iatrogenic Fistula in Hemodialysis Patients: An Alternative Approach to Thrombectomy of Arteriovenous Graft (AVG) Thrombosis","authors":"R. Dukkipati, A. Benjo, A. Jimenez, I. Lukitsch, Gift Echefu, D. Kumbala","doi":"10.1155/2022/2417980","DOIUrl":"https://doi.org/10.1155/2022/2417980","url":null,"abstract":"Arterial venous (AV) fistula is the first choice of vascular access to perform hemodialysis in the vast majority of suitable patients followed by arteriovenous grafts (AVG). An iatrogenic fistula can occur when a second vein adjacent to the graft is punctured and the needle traverses the vein. In normal circumstances, this has no clinical repercussions and does not need correction, and in prior reports, it has helped to maintain the patency of partially occluded grafts but rarely can lead to thrombosis of the graft due to reduced flow and pressure in the graft lumen. We report here what we believe is a unique approach to perform thrombectomy of an occluded graft in a 71-year-old patient on hemodialysis to avoid placement of tunneled hemodialysis catheters and complications associated with catheters. When the outflow of basilic vein in this patient was thrombosed and could not be traversed, we successfully used an iatrogenic fistula as main outflow vein for the graft and created an alternative vein for drainage thus avoiding placement of a tunneled catheter for hemodialysis.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86074532","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}
引用次数: 1
Spontaneous Dissections of Bilateral Internal Carotid and Vertebral Arteries due to Intractable Vomiting 顽固性呕吐引起的双侧颈内动脉和椎动脉自发夹层
Case Reports in Vascular Medicine Pub Date : 2022-04-11 DOI: 10.1155/2022/8156047
Gift Echefu, R. Mahat, Raju Vatsavai, S. Zuckerman
{"title":"Spontaneous Dissections of Bilateral Internal Carotid and Vertebral Arteries due to Intractable Vomiting","authors":"Gift Echefu, R. Mahat, Raju Vatsavai, S. Zuckerman","doi":"10.1155/2022/8156047","DOIUrl":"https://doi.org/10.1155/2022/8156047","url":null,"abstract":"In young adults, spontaneous craniocervical arterial dissections (sCAD), which involve the major arteries of the head and neck, are associated with an increased risk of stroke. sCAD occurs in the absence of major trauma as seen in traumatic craniocervical artery dissection. It may affect unilateral or bilateral carotid or vertebral arteries. Cases of spontaneous bilateral carotid and vertebral artery dissections occurring simultaneously are extremely rare. We present a case of a 49-year-old female with no history of arteriopathy who presented with aphasia and right upper extremity weakness and was found to have dissections in bilateral extracranial and intracranial carotid arteries, as well as the bilateral vertebral arteries. She had symptomatic improvement with antithrombotic therapy and aggressive outpatient rehabilitation.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"29 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76609466","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}
引用次数: 3
Successful Radiofrequency Ablation of the Right Lateral Accessory Pathway with Modified Carpentier Reconstruction Surgery in a Patient with Ebstein Anomaly Concomitant of Secundum Atrial Septal Defect, Atrial Fibrillation, and Wolff–Parkinson–White Syndrome 改良Carpentier重建术射频消融右外侧副通道成功治疗Ebstein异常合并第二房间隔缺损、心房颤动和Wolff-Parkinson-White综合征患者
Case Reports in Vascular Medicine Pub Date : 2022-04-04 DOI: 10.1155/2022/8343943
Van Dan Nguyen, Xuan Tuan Nguyen, Van Tung Pham, L. Pham
{"title":"Successful Radiofrequency Ablation of the Right Lateral Accessory Pathway with Modified Carpentier Reconstruction Surgery in a Patient with Ebstein Anomaly Concomitant of Secundum Atrial Septal Defect, Atrial Fibrillation, and Wolff–Parkinson–White Syndrome","authors":"Van Dan Nguyen, Xuan Tuan Nguyen, Van Tung Pham, L. Pham","doi":"10.1155/2022/8343943","DOIUrl":"https://doi.org/10.1155/2022/8343943","url":null,"abstract":"Ebstein anomaly (EA) results from the failure of proper delamination of the tricuspid valve leaflets from the right ventricle (RV) myocardium. The severity of EA occurs on a spectrum that results in varying degrees of tricuspid regurgitation, atrial dilation, RV dilation, and dysfunction. These effects have the potential to create substrates that can give rise to atrial arrhythmia, ventricular arrhythmia, and a greater incidence of Wolff–Parkinson–White (WPW) syndrome Wackel et al. (2018) accounting for 0.5% of all congenital heart diseases (Oh et al. 1985). In the case of atrial fibrillation and WPW, it is very dangerous for the patient because of hemodynamic compromise, syncope, and sudden death. In this case report, we share our experience in using radiofrequency ablation to ablate right lateral accessory pathway, with modified Carpentier technique in operation to treat an adult patient diagnosed with Ebstein anomaly, atrial septal defect, atrial fibrillation, and WPW syndrome.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"54 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83070147","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}
引用次数: 0
Digital Gangrene: An Unusual Manifestation of Non-Hodgkin Lymphoma 指坏疽:非霍奇金淋巴瘤的一种不寻常的表现
Case Reports in Vascular Medicine Pub Date : 2022-03-02 DOI: 10.1155/2022/8963753
M. S. Momen Majumder, Shamim Ahmed, Tajkia Haque, S. Haq, S. Chakravarty, M. Shahin, D. M. F. Osmany, J. Rasker
{"title":"Digital Gangrene: An Unusual Manifestation of Non-Hodgkin Lymphoma","authors":"M. S. Momen Majumder, Shamim Ahmed, Tajkia Haque, S. Haq, S. Chakravarty, M. Shahin, D. M. F. Osmany, J. Rasker","doi":"10.1155/2022/8963753","DOIUrl":"https://doi.org/10.1155/2022/8963753","url":null,"abstract":"Background Non-Hodgkin lymphomas (NHLs) comprise a group of haematologic malignancies with different histologic subtypes. The clinical picture varies from indolent to aggressive presentation and nodal (lymphadenopathy) to extranodal (central nervous system, gastrointestinal, cutaneous plaque, or ulcer) involvement. Digital gangrene is seldom reported. Here, we describe a patient with pain and blackening of all fingers and toes as presenting symptoms of NHL. Case Presentation. A 32-year-old male weaver had been smoking three to five cannabis-containing cigarettes daily for about ten years and methamphetamine four to five tablets daily for five years. He had no history of Raynaud's phenomenon, fever, cough, weight loss, skin rash, joint pain, and atherogenic or thrombogenic risk factors. We found normal blood pressure and absent peripheral pulses in arms and legs, dry gangrene of all fingers and toes, generalized lymphadenopathy, and hepatomegaly with ascites. The chest X-ray was normal, as were blood sugar, lipid profile, and hepatic and renal function. Rheumatoid factor, antinuclear and antiphospholipid antibodies, C-ANCA and P-ANCA, hepatitis B and C, and HIV were negative. CT abdomen revealed hepatosplenomegaly with multiple intra-abdominal lymphadenopathies. The peripheral angiogram showed 90-99% stenosis of radial and dorsalis pedis arteries with normal proximal vessels. Diagnosis of non-Hodgkin lymphoma was confirmed by histopathology of cervical lymph node (diffuse type), immunohistochemically subtyped as peripheral T cell lymphoma (not otherwise specified). The digital ischemia worsened despite cessation of cannabis and methamphetamine and starting CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) treatment, making amputation necessary. Conclusion We present, to our knowledge, the first report of peripheral T cell lymphoma, NOS presenting with gangrene in all digits complicated by methamphetamine and cannabis abuse. This uncommon vascular manifestation of non-Hodgkin lymphoma may cause a diagnostic dilemma and delayed initiation of treatment.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"30 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81586563","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}
引用次数: 1
A Novel Approach for Transvenous Embolization of Dural Arteriovenous Fistula Using a Balloon and a Coil as Walls: Case Presentation 一种以球囊和线圈为壁经静脉栓塞硬脑膜动静脉瘘的新方法:病例报告
Case Reports in Vascular Medicine Pub Date : 2022-02-25 DOI: 10.1155/2022/5164452
Kenji Fukutome, S. Aketa, Tsukasa Nakajima, Hiromichi Hayami, H. Sasaki, Ryuta Matsuoka, Rinsei Tei, Y. Shin, Y. Motoyama
{"title":"A Novel Approach for Transvenous Embolization of Dural Arteriovenous Fistula Using a Balloon and a Coil as Walls: Case Presentation","authors":"Kenji Fukutome, S. Aketa, Tsukasa Nakajima, Hiromichi Hayami, H. Sasaki, Ryuta Matsuoka, Rinsei Tei, Y. Shin, Y. Motoyama","doi":"10.1155/2022/5164452","DOIUrl":"https://doi.org/10.1155/2022/5164452","url":null,"abstract":"Background Transvenous embolization (TVE) for dural arteriovenous fistula (DAVF) is difficult depending on an accessible route. Reported herein is a case of transvenous embolization using a balloon and a coil as “walls.” Case Description. A 56-year-old male patient presented with a 1-month history of mild motor aphasia. The magnetic resonance imaging showed a hemorrhagic lesion in his left temporal lobe, and the cerebral angiography showed a DAVF, with parasinus shunt points near the torcula and the left transverse sinus. Access to the shunt point was very difficult; however, TVE was performed using a balloon as a wall. Furthermore, all lesion embolization was possible using a coil as a wall. Conclusions Using a balloon or coil as a wall during a TVE is useful.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74620807","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}
引用次数: 0
85-Year-Old Postsurgical Complex Patient Successfully Managed Remotely at the Novel Mayo Clinic's Hospital at Home 85岁高龄的复杂术后患者在新梅奥诊所居家医院成功远程管理
Case Reports in Vascular Medicine Pub Date : 2022-02-25 DOI: 10.1155/2022/1439435
M. Paulson, Ricardo A. Torres-Guzman, Francisco R. Avila, Karla C. Maita, John P. Garcia, A. Eldaly, Luiza Palmieri-Serrano, A. Forte, Jonathan C Thompson, M. Maniaci
{"title":"85-Year-Old Postsurgical Complex Patient Successfully Managed Remotely at the Novel Mayo Clinic's Hospital at Home","authors":"M. Paulson, Ricardo A. Torres-Guzman, Francisco R. Avila, Karla C. Maita, John P. Garcia, A. Eldaly, Luiza Palmieri-Serrano, A. Forte, Jonathan C Thompson, M. Maniaci","doi":"10.1155/2022/1439435","DOIUrl":"https://doi.org/10.1155/2022/1439435","url":null,"abstract":"An 85-year-old male presented to the podiatry clinic following a 1st to 5th left toe amputation as a complication of severe peripheral arterial disease and nonhealing wound despite endovascular intervention with an angiogram. At the visit, cellulitis with gangrene of the surgical site was noted. The patient was admitted to the brick and mortar (BAM) hospital and taken to surgery for a transmetatarsal amputation of the left limb. In the immediate postoperative period, the incisional margins appeared dusky creating concern for flap viability. The medical team recommended a vascular bypass versus a below-knee amputation. However, given the age, comorbidities, and nutritional status, the family refused further surgical intervention. As such, Mayo Clinic's home hospital program, Advanced Care at Home (ACH), was consulted for continued nonsurgical acute management at home. The patient was transferred to ACH and transported home three days after BAM admission to continue IV antibiotic therapy and wound care. Discharge from ACH occurred 11 days after admission to the BAM hospital. This case highlights the importance of developing health care alternatives to traditional hospitalization and demonstrates that ACH can manage highly complex, elder postoperative patients from the comfort of their homes.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"33 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78959100","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}
引用次数: 2
Angiographic Embolization with Histoacryl in Combination with Direct Injection of Bone Cement of an Intraosseous Venous Malformation of the Mandible: Report of a Case with 22-Year Follow-Up 组织丙烯动脉造影栓塞联合骨水泥直接注射治疗下颌骨骨内静脉畸形:22年随访1例报告
Case Reports in Vascular Medicine Pub Date : 2022-02-16 DOI: 10.1155/2022/6842968
A. Berbéri, G. Aoun, G. Aad, S. Khairallah, G. A. Chedid
{"title":"Angiographic Embolization with Histoacryl in Combination with Direct Injection of Bone Cement of an Intraosseous Venous Malformation of the Mandible: Report of a Case with 22-Year Follow-Up","authors":"A. Berbéri, G. Aoun, G. Aad, S. Khairallah, G. A. Chedid","doi":"10.1155/2022/6842968","DOIUrl":"https://doi.org/10.1155/2022/6842968","url":null,"abstract":"Vascular malformations of the maxillofacial region are unusual, and they occur more rarely in bone than in soft tissue. Mandibular intraosseous vascular lesions represent 0.5-1.0% of all bone tumors, and they are classified as venous malformation, lymphatic malformation, arterial malformation, arteriovenous malformations, and arteriovenous fistulae. Venous malformation is the most common vascular malformation, accounting for 44-64% of all vascular malformations, and is considered a low-flow malformation. Endovascular therapy as selective angiographic embolization is considered as the first-choice treatment associated or not with emboli injections with a success rate of 70%, and this evades mutilating surgery and related sequelae. We report a case of mandibular venous malformation on a 45-year-old female complaining of unilateral swelling of the left body of the mandible with facial deformation. The computed tomography scan images and the T1-weighted MR images showed a lesion that expresses an expansible lesion in the spongy bone of the left of the mandible with a buccal cortical rupture. Signal voids were not identified, suggesting a low-flow vascular lesion. The T2-weighted images exposed hypersignals; accordingly, a vascular lesion was suspected. The treatment was done under locoregional analgesia; after selective angiography, direct histoacryl injection was completed, followed by bone cement injection. The patient was followed yearly since1998. Radiological images of 10-year follow-up MRI showed a stabilization of the lesion without any new extensions. The panoramic radiograph after 22 years showed a bone formation inside the body of the mandible. The long follow-up period and the absence of any complications are favorable for the adopted treatment plan.","PeriodicalId":9632,"journal":{"name":"Case Reports in Vascular Medicine","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79807237","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}
引用次数: 0
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