A 10-year follow-up of extracranial–intracranial bypass for the treatment of bilateral giant internal carotid artery aneurysms in a patient with fibromuscular dysplasia: case report

2010 ◽  
Vol 152 (12) ◽  
pp. 2191-2195 ◽  
Author(s):  
Yan Ma ◽  
Meng Li ◽  
Hongqi Zhang ◽  
Feng Ling
Neurosurgery ◽  
1982 ◽  
Vol 10 (1) ◽  
pp. 39-43 ◽  
Author(s):  
Ralph P. Wells ◽  
Robert R. Smith

Abstract The natural course of fibromuscular dysplasia (FMD) of the internal carotid artery (ICA). a stenosing angiopathy associated with cerebrovascular insufficiency, has not been described. A search of medical records located 16 female patients with angiographically demonstrated FMD of the ICA. The identical twin of 1 patient was included in the registry on the basis of noninvasive studies consistent with FMD of the ICA. The mean age at diagnosis was 58 years. Follow-up examinations were performed an average of 3.8 years after diagnosis (range, 1 to 9 years); the evaluation included clinical, angiographic, and Doppler studies. Fifteen patients showed no evidence of progression of FMD, whereas 2 patients with coincident atherosclerotic disease had suffered strokes. One patient had undergone surgical dilatation of the ICA. 3 had received oral anticoagulants, and 13 had received either aspirin or no specific therapy. In light of the apparently benign clinical course of uncomplicated FMD of the ICA, it is concluded that dilatation is rarely warranted.


2003 ◽  
Vol 10 (2) ◽  
pp. 182-189 ◽  
Author(s):  
Stephen M. Kubaska ◽  
Roy K. Greenberg ◽  
Daniel Clair ◽  
Gregory Barber ◽  
Sunita D. Srivastava ◽  
...  

Purpose: To report several cases illustrating the feasibility and mid-term efficacy of deploying a self-expanding stent-graft to treat traumatic ruptures, pseudoaneurysms, and a spontaneous dissection of the internal carotid artery (ICA). Case Reports: One patient suffered a stab wound and another developed a large pseudoaneurysm years after a gunshot to the neck. The third patient presented with a spontaneous rupture in the setting of fibromuscular dysplasia, and the final patient developed a pseudoaneurysm following carotid endarterectomy in an irradiated neck. All 4 patients were successfully treated with Wallgrafts deployed in the ICA using either an open carotid (first 3 cases) or percutaneous approach (fourth patient). There were no adverse neurological events. During a mean 16-month follow-up (range 6–24), duplex ultrasound and CT scanning found no evidence of restenosis, occlusion, or persistent perfusion of the pseudoaneurysm, which was noted to decrease in all cases. Conclusions: The thin-walled fabric of the Wallgraft appears capable of completely excluding the pseudoaneurysm, resulting in decreased aneurysm size overtime.


Stroke ◽  
1983 ◽  
Vol 14 (5) ◽  
pp. 815-818 ◽  
Author(s):  
J A Garcia-Merino ◽  
J A Gutierrez ◽  
J J Lopez-Lozano ◽  
M Marquez ◽  
F Lopez ◽  
...  

2016 ◽  
Vol 130 (6) ◽  
pp. 596-599 ◽  
Author(s):  
M Roos ◽  
I Butler

AbstractBackground:Extracranial internal carotid artery pseudoaneurysm is very rare in children.Method:This paper discusses the case of a boy, aged two years and six months, who presented with an enlarging neck mass and unilateral bloody otorrhoea. Special investigations revealed an extracranial internal carotid artery pseudoaneurysm.Results:The patient made a full recovery after endovascular occlusion of the internal carotid artery and pseudoaneurysm using coils. At six months’ follow up, the internal carotid artery and pseudoaneurysm remained excluded from the circulation. The patient did not display any neurological deficits during hospital stay or follow up.Conclusion:This paper reports on one of the youngest patients documented to date who presented with an internal carotid artery pseudoaneurysm, possibly secondary to ear infection. Although rare, this condition should be excluded in children presenting with a mass of the neck or pharynx because of the dire consequences if left undiagnosed and untreated.


2005 ◽  
Vol 29 (1) ◽  
pp. 9-13
Author(s):  
Wei Zhou ◽  
Ruth L. Bush ◽  
Peter H. Lin ◽  
Megan D. Hodge ◽  
Deborah D. Felkai ◽  
...  

Purpose The diagnosis of carotid artery fibromuscular dysplasia is usually made with conventional angiography performed to evaluate a suspected carotid stenosis. The ultrasound findings with fibromuscular dysplasia have not been well described. This study was performed to assess the characteristics of carotid artery fibromuscular dysplasia with duplex ultrasonography. Methods The hospital records for all patients who had carotid duplex ultrasonography were reviewed from January 2000 to October 2003. Patients with findings suspicious for fibromuscular dysplasia formed the basis of this study. The patient demographics, their presenting symptoms, and ultrasound findings were analyzed. Results Carotid duplex studies were performed on 9157 patients during the study period. The presumptive diagnosis of fibromuscular dysplasia was made in 13 female patients (1.2%), with a mean age of 67 ± 10 years (range, 52-79 years). Patients were referred for asymptomatic carotid bruits ( n = 10, 77%) or transient ischemic attack ( n = 3, 23%). Both mid and distal internal carotid artery involvement were seen in five patients (38%), whereas eight patients (62%) had disease isolated to the distal internal carotid artery. Bilateral carotid artery involvement occurred in eight patients (62%). A consistent finding in all patients was multiple areas of alternating focal thickening with thin, dilated arterial walls. Other sonographic findings included velocity increases (mean, 181 cm/sec; range, 135-318 cm/sec), color flow disturbance, and scarcity of plaque in the suspected arterial segment. Magnetic resonance angiography or carotid angiography was performed on seven (54%) patients, confirming the ultrasound diagnoses. One symptomatic patient was successfully treated with open graduated endoluminal dilatation. One patient with asymptomatic carotid bruit underwent carotid stent placement for rapid progression of the disease. No disease progression was seen on follow-up duplex examination in the remaining group, and no patient became symptomatic. Conclusions Fibromuscular dysplasia should be suspected in female patients with high-grade mid to distal carotid artery stenosis without significant atherosclerotic disease. This study demonstrates the usefulness of duplex ultrasound as both a screening test and diagnostic examination for carotid artery fibromuscular dysplasia. Follow-up is warranted in these patients.


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