Abstract 1122‐000160: Transvenous Embolization Technique: A Modern Strategy for Anterior Ethmoidal Dural Arteriovenous Fistulas

Author(s):  
Mais N Al‐Kawaz ◽  
Mais N Al‐Kawaz ◽  
Maximilian J Bazil ◽  
Stavros Matsoukas ◽  
Tomoyoshi Shigematsu ◽  
...  

Introduction : Ethmoidal dural arteriovenous fistulae (AVF) are rare intracranial lesions and account for 2–3% of all dAVF. They are often supplied by the ethmoidal or falcine branches of the ophthalmic artery and typically drain into a cortical vein then into the superior sagittal sinus (SSS). Current available treatment options include surgical resection and endovascular embolization via transarterial and transvenous routes. Prior studies have solely compared surgical and transarterial endovascular treatment approaches. Reports of the transvenous approach remain scarce in the literature. Methods : We performed a retrospective review for anterior ethmoidal (AE)‐dAVFs treated with transvenous embolization by our practice between August 2018 and August 2021. Four patients with 5 dAVFs were identified. We describe the presentation, treatment, and outcome of these cases. Results : We describe four patients with AE‐dAVF. Case 1 is a 33‐year‐old man with a previously treated basal ganglia arteriovenous malformation achieving cure. He was lost for follow up for three years and returned with symptoms of peri‐orbital headache and blurry vision. Diagnostic angiography revealed a dAVF arising from the cribriform plate with arterial supply derived from bilateral AE arteries and venous drainage via a common cortical frontal interhemispheric vein to the anterior third of the SSS. Transvenous embolization was achieved and liquid embolic was injected into the vein with retrograde penetration to the fistulous point. Follow‐up angiography revealed obliteration of the dAVF. Case 2 is a 23‐year‐old man with chronic headache who was found to have a right sided ethmoidal dAVF arising from the right ophthalmic artery for which he underwent successful embolization through a transarterial approach. Follow‐up angiography demonstrated occlusion of the treated fistula and new left sided ethmoidal AVF arising from the left ophthalmic artery with a single draining cerebral vein which drains into the anterior third of the SSS. Transvenous embolization was achieved via coiling. Follow up angiography also showed complete occlusion of the dAVF. Case 3 was a 67‐year‐old woman who presented with a Cognard type III right ethmoidal dAVF with arterial feeders through surpra‐orbital branches of the right ophthalmic artery, draining into a frontal cortical vein leading to the SSS. The patient underwent transvenous embolization using coils. Case 4 was a 64‐year‐old woman who presented with scalp tenderness. Diagnostic angiography revealed a left AE‐dAVF. Transvenous embolization with complete occlusion was achieved using a combination of liquid embolic and coil embolization. No adverse events were encountered during or after embolization, but long‐term outcome has yet to be collected for cases 3 and 4. There were no neurologic procedural complications. Conclusions : This small case series shows that transvenous embolization is a feasible, effective, and safe alternative to surgery. Larger prospective studies are needed to further validate this treatment approach in patients with ethmoidal dAVF.

2011 ◽  
Vol 17 (1) ◽  
pp. 87-92 ◽  
Author(s):  
Y. Wang ◽  
N. Xu ◽  
Q. Luo ◽  
Y. Li ◽  
L. Sun ◽  
...  

We sought to assess the feasibility of using thermosensitive chitosan/β-glycerophosphate for embolotherapy. The renal arteries in nine rabbits were embolized with chitosan/β-glycerophosphate. The animals were studied angiographically and sacrificed at one week (n = 3), four weeks (n = 3), and eight weeks (n = 3) after embolotherapy. Histology was obtained at these three time points. Delivery of chitosan/β-glycerophosphate was successful in all cases. Complete occlusion was achieved in all cases. No recanalization was observed in the follow-up angiograms. No untoward inflammatory reactions were observed in the target renal arteries and infarcted kidneys during the histological examinations. Our preliminary feasibility evaluation in rabbit renal arteries indicates that C/GP is a satisfactory embolization agent.


2011 ◽  
Vol 56 (No. 8) ◽  
pp. 416-422 ◽  
Author(s):  
R. Tamburro ◽  
M. Pietra ◽  
G. Militerno ◽  
A. Diana ◽  
A. Spadari ◽  
...  

Lung lobe torsion (LLT) is an uncommon pathology in small animal practice. In large breed dogs LLT effects are localized mainly to the middle lobe of the right lung. This report describes a case of left cranial lung torsion in a Bernese Mountain dog: the patient was referred with a two-day history of asthenia, anorexia, dyspnea and haemoptysis. No trauma was reported. Physical examination showed the presence of bilateral pleural effusion confirmed by radiography and ultrasonography. Broncoscopy revealed that the left cranial lobe appeared to be compressed laterally with complete occlusion of the lumen. Thoracoscopy was performed to exclude other pathologies of the pleural space. The pathological lobe was removed. Histological examination revealed aspects consistent with lung lobe torsion. Clinical follow up carried out after three months showed a normal clinical course.


2021 ◽  
pp. neurintsurg-2021-017530.rep
Author(s):  
Caleb Rutledge ◽  
Jacob F Baranoski ◽  
Joshua S Catapano ◽  
Ashutosh P Jadhav ◽  
Felipe C Albuquerque ◽  
...  

A man in his 50s presented 1 month after an automobile accident with worsening headaches and an enlarging chronic left subdural haematoma (SDH). He underwent left middle meningeal artery (MMA) embolisation. Due to tortuosity at its origin, we were unable to catheterise the MMA distally. Only proximal coil occlusion at the origin was performed. Follow-up interval head CT showed an increase in the size of the SDH with new haemorrhage, worsening mass effect and midline shift. However, he remained neurologically intact. Contralateral embolisation of the right MMA was performed with a liquid embolic agent. His headaches improved, and a follow-up head CT 3 months later showed near-complete resolution of the SDH.


2017 ◽  
Vol 24 (2) ◽  
pp. 189-196 ◽  
Author(s):  
Masaki Sato ◽  
Takashi Izumi ◽  
Noriaki Matsubara ◽  
Masahiro Nishihori ◽  
Shigeru Miyachi ◽  
...  

Background This study aimed to evaluate the detailed location and the number (single or multiple) of cavernous sinus dural arteriovenous fistula (CSDAVF) shunted pouches as well as the relationship between the characteristics of shunted pouch(es) and the treatment outcome of transvenous embolization for CSDAVF. Methods A total of 23 consecutive patients with CSDAVFs who underwent angiogram and transvenous embolization were retrospectively analyzed. Shunted pouches were assessed using three-dimensional angiogram and multiplanar reformatted image obtained from the rotational angiogram data. Results Of the 23 patients with CSDAVFs, 40 shunted pouches were identified. Twelve CSDAVFs had a single shunted pouch, and 11 had multiple shunted pouches. The mean CSDAVF with multiple shunted pouches was 2.5. The shunted pouches were more often found in the posterior compartment of the CS, which was connected with the intercavernous sinus (23/40; 57.5%). In 12 CSDAVFs with a single shunted pouch, 10 were treated with selective embolization and complete occlusion was achieved during the follow-up. Two CSDAVFs with single shunted pouch were just observed without intervention, and DAVFs disappeared spontaneously during the follow-up period. In 11 CSDAVFs with multiple shunted pouches, eight were treated with selective embolization and three with sinus embolization. In six of eight (75%), complete occlusion was achieved following selective embolization, but two of eight (25%) recurred and required retreatment. Conclusions Rotational angiography data suggested that the shunted pouches of CSDAVFs were mostly located in the posterior compartment of the CS connected with the intercavernous sinus. Selective embolization for CSDAVFs with a single shunted pouch is the first-line treatment alternative to sinus packing, and selective embolization with multiple shunted pouches will be a considerable treatment option.


Author(s):  
Qiang Fan ◽  
Yunfei Ling ◽  
Qi An

In this case report, we describe a rare large right ventricular fibroma with sudden chest pain in a 9 year old child. The tumor was successfully surgical removed under cardiopulmonary bypass, but there was only a small remnant of the tumor to avoid rupture of the right ventricle and injury to the tricuspid valve. Pathological examination confirmed that the tumor was fibrous borderline tumor. The patient’s heart function and the size of atrium and ventricles were normal, and there was no tricuspid regurgitation at 3-months follow-up. It was reported that the age less than 17 years old at time of diagnosis are associated with a poor prognosis, the long term outcome for this children patient needs further follow-up.


2010 ◽  
Vol 16 (3) ◽  
pp. 249-254 ◽  
Author(s):  
J. Zhang ◽  
R. Zhang ◽  
Z. Wu ◽  
X. Lv ◽  
B. Liu

We evaluated the results of endovascular management of patients with mid-basilar artery aneurysm (mBAA). During a seven year period, 14 patients (mean age 39.6 years, male/female ratio 1:1) with mBAA were treated with endovascular techniques at our institute. Pretreatment clinical grades were determined using the Hunt-Hess scale. Outcome was evaluated using the Glasgow Outcome Scale scores (GOS) during a mean follow-up period of 15.6 months (range, three to 70 months). Fourteen patients with 15 mBAAs were treated endovascularly. Four (28.6%) patients died of rebleeding within one day after embolization. In ten mBAAs, immediate postprocedural angiograms showed that complete occlusion was achieved, subtotal occlusion in one, and incomplete occlusion in four. Follow-up angiographic results in ten patients confirmed complete occlusion of 11 aneurysms. Long-term outcome was good (GOS Score 4 or 5) in ten patients (71.4%) and fatal (GOS Score 1) in four (28.6%). Favorable overall long-term outcome can be achieved in 78.6% patients with mBAAs. Endovascular management of mBAAs is an effective treatment in the long-term. In our experience, the natural history of mBAAs is dismal.


2017 ◽  
Vol 23 (6) ◽  
pp. 609-613 ◽  
Author(s):  
Tamás Németh ◽  
László Szakács ◽  
Zsolt Bella ◽  
Valéria Majoros ◽  
Pál Barzó ◽  
...  

Background We report a case of bilateral malignant otitis externa complicated with bilateral petrous internal carotid artery pseudoaneurysms and their successful treatment with a flow diverter. Case report A 68-year-old woman with serious complications of type II diabetes mellitus had malignant otitis externa on the right side. She was treated with combined antibiotic therapy and underwent mastoidectomy for mastoiditis. She presented at our hospital with acute hemorrhage from the right external auditory canal. The emergency computed tomography (CT) angiography revealed a multiobulated pseudoaneurysm at the petrous segment of the right internal carotid artery. The pseudoaneurysm was treated with a 5 × 40-mm Surpass flow diverter. Three months later, she developed a malignant external otitis on the left side. As the infection progressed, a left-sided mastoiditis, a brain abscess, and a pseudoaneurysm at the petrous segment of the left internal carotid artery developed. The pseudoaneurysm caused bleeding from the left ear, and was treated with a 5 × 50-mm Surpass flow diverter. No recurrent bleeding was observed. Four months later, a follow-up angiography showed complete occlusion of the pseudoaneurysm on the left side, but a residual aneurysm could be detected on the right side. One year after the first intervention, the follow-up CT and magnetic resonance angiography revealed the complete occlusion of the aneurysms bilaterally. Conclusion The use of a flow diverter appears to be an efficient and safe method to occlude carotid pseudoaneurysms even in an inflammatory milieu.


2020 ◽  
pp. neurintsurg-2020-016790
Author(s):  
Petra Cimflova ◽  
Enes Özlük ◽  
Bora Korkmazer ◽  
Ramiz Ahmadov ◽  
Elif Akpek ◽  
...  

BackgroundIndications for flow diversion stent (FDS) treatment are expanding. However, there is still a lack of evidence for the long-term outcome in distally located aneurysms in the M2 segment of the middle cerebral artery (MCA) and beyond.MethodsConsecutive subjects (from June 2013 to August 2020) with MCA aneurysms in the M2 segment or beyond treated with FDS were reviewed retrospectively. The primary endpoints for clinical safety were the absence of mortality, stroke event, re-rupture of the aneurysm, and worsening of clinical symptoms. The primary endpoint for treatment efficacy was complete/near-complete occlusion at follow-up after 12 months.Results23 patients were identified: 7 aneurysms were located in the M2 segment of the MCA, 4 in the M2-M3 bifurcation, 2 in M3, 3 in M3-4 branching, and 2 in M4; 5 aneurysms were located in M2 with extension into the M1-M2 bifurcation. 13 aneurysms were of fusiform morphology, 8 sacculofusiform, and 2 saccular. 16 aneurysms were of highly suspected dissecting etiology. The median diameter of the parent vessel was 2.1 mm proximally and 2 mm distally. The median time of the follow-up was 30 months (range 16 months to 6 years). Complete/near complete occlusion was observed in 14/20 patients (70%) and one stable remodeling (5%) was seen at 12 months. 22 patients (95.6%) had an excellent clinical outcome (mRS 0–1) at 6 months. Technical challenges associated with the deployment of FDS occurred in 8.7% of cases. Severe complications, intraparenchymal hemorrhage and re-rupture of the aneurysm occurred in 2 patients (8.7%).ConclusionFlow diversion of distally located aneurysms is technically feasible with low morbidity and mortality.


2021 ◽  
Vol 14 (4) ◽  
pp. e017530
Author(s):  
Caleb Rutledge ◽  
Jacob F Baranoski ◽  
Joshua S Catapano ◽  
Ashutosh P Jadhav ◽  
Felipe C Albuquerque ◽  
...  

A man in his 50s presented 1 month after an automobile accident with worsening headaches and an enlarging chronic left subdural haematoma (SDH). He underwent left middle meningeal artery (MMA) embolisation. Due to tortuosity at its origin, we were unable to catheterise the MMA distally. Only proximal coil occlusion at the origin was performed. Follow-up interval head CT showed an increase in the size of the SDH with new haemorrhage, worsening mass effect and midline shift. However, he remained neurologically intact. Contralateral embolisation of the right MMA was performed with a liquid embolic agent. His headaches improved, and a follow-up head CT 3 months later showed near-complete resolution of the SDH.


2016 ◽  
Vol 12 (2) ◽  
Author(s):  
Rajgopal Shenoy ◽  
Gabriel Rodrigues ◽  
Vikas Jain ◽  
Sohil Ahmed Khan

Objective: The present study envisages evaluating the clinical presentation, diagnosis, management, with particular reference to pharmacological and anesthetic considerations, and outcome in patients with pheochromocytoma. Design: A retrospective study. Place and Duration of Study: The study was conducted at the Department of Surgery, Kasturba Medical College Hospital, Manipal, India from January 1, 1996 to December 31, 2003. Patients and Methods: Seventeen patients diagnosed to have pheochromocytoma were included for this study. Our assessment of age at presentation, sex, presenting complaints with details of hypertension (HT), diagnostic tests, surgical procedure and follow-up was based on patient records. Results: Peak incidence was observed in 40-50 years age group, with male preponderance. All the patients had diastolic HT of more than 100 mm of Hg at presentation. Systolic blood pressures (SBP) were between 150 mm Hg to 230 mm Hg, with mean of 170 mm Hg; nine patients presented with persistent HT and seven had paroxysmal HT. One patient infact presented with hypotension due to septic shock and was incidentally detected to have an adrenal tumor. Computed tomography (CT) scan and urinary levels of vanillylmandelic acid (VMA) were mainstay of diagnosis. These patients had adequate preoperative control of HT. All patients underwent exploration of the tumor by an extraperitoneal approach. 70% tumors were on the right and 30% were on the left side. Histopathologically, all the tumors were benign except for one, which was malignant. An average of three to five units of blood transfusion was required and mean operating time was 4.5 hours. Six patients had extensive intra-operative blood pressure (BP) fluctuation, but were adequately managed by the anesthetic team. One patient with post-operative pulmonary edema died in our series; rest all the patients are on regular follow-up, till date and doing well. Conclusion: Pheochromocytoma is an important cause of endocrine HT. Elevated urinary VMA is diagnostic of this tumor with imaging studies used to localize the tumor. Adrenalectomy results in complete cure of HT with an excellent long-term outcome.


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