Failure of Primary Percutaneous Angioplasty and Stenting in the Prevention of Ischemia in Moyamoya Angiopathy

被引:42
作者
Khan, Nadia [1 ]
Dodd, Robert [1 ,2 ,3 ]
Marks, Michael P. [1 ,2 ,3 ]
Bell-Stephens, Teresa [1 ]
Vavao, Joli [1 ]
Steinberg, Gary K. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurosurg, Stanford Stroke Ctr, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Radiol, Stanford Stroke Ctr, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Stanford Inst Neuroinnovat & Translat Neurosci, Stanford, CA 94305 USA
关键词
Angioplasty; Moyamoya; Wingspan stent; DISEASE; REVASCULARIZATION; PROGRESSION; STENOSIS;
D O I
10.1159/000320253
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Moyamoya disease (MMD) is an idiopathic progressive arteriopathy affecting the proximal intracranial vasculature. To date only 4 case reports on intracranial angioplasty or stenting as treatment of this disease exist. We present 5 adult patients with MMD who failed angioplasty and/or stenting who remained symptomatic despite endovascular treatment or presented with recurrent symptoms and recurrence of stenosis/occlusion on angiography requiring subsequent extracranial-intracranial revascularization. Methods: Five adult MMD patients who underwent endovascular treatment with angioplasty or stenting were referred for further evaluation and treatment from outside hospitals. Data were collected from clinical referral notes and angiograms or reports. All patients underwent repeat 6-vessel cerebral angiography to assess the extent of disease and results of prior endovascular treatment. Results: Six endovascular procedures were performed in all 5 patients. Internal carotid artery (ICA) balloon angioplasty and Wingspan stenting was performed in 2 patients (3 arteries). One patient had ICA-M1 angioplasty without stenting. Two patients had M1 angioplasty and Wingspan stenting. All patients developed repeat transient ischemic attacks following treatment attributable to the vascular territories of endovascular treatment. Repeat endovascular treatment was performed in 3 patients at a mean of 4 months (range = 2-6). Two went on to a third endovascular treatment due to progression of disease in the angioplastied/stented vessel. The average time of symptom recurrence after initial endovascular therapy was 1.8 months (0-4 months). Follow-up angiography when referred to our institution demonstrated 70-90% instent restenosis of the stented vessel in 3 and occlusion in 1 patient. Due to persistence of symptoms cerebral revascularization was performed in all patients. Conclusion: MMD is a progressive angiopathy. Angioplasty and stenting may temporarily improve the cerebral blood flow and decrease cerebral ischemic events but do not appear to be durable nor provide long-term prevention against future ischemic events. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:147 / 153
页数:7
相关论文
共 22 条
[1]   Angiographic patterns of Wingspan in-stent restenosis [J].
Albuquerque, Felipe C. ;
Levy, Elad I. ;
Turk, Aquilla S. ;
Niemann, David B. ;
Aagaard-Kienitz, Beverly ;
Pride, G. Lee, Jr. ;
Purdy, Phillip D. ;
Welch, Babu C. ;
Woo, Henry H. ;
Rasmussen, Peter A. ;
Hopkins, L. Nelson ;
Masaryk, Thomas J. ;
McDougall, Cameron G. ;
Fiorella, David J. .
NEUROSURGERY, 2008, 63 (01) :23-27
[2]   Endovascular treatment for moyamoya disease in a Caucasian twin with angioplasty and Wingspan stent [J].
Drazin, Doniel ;
Calayag, Mark ;
Gifford, Edward ;
Dalfino, John ;
Yamamoto, Junichi ;
Boulos, Alan S. .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2009, 111 (10) :913-917
[3]  
ELHAKAM LM, 2010, J CHILD NEUROL
[4]  
Fukui M, 1997, CLIN NEUROL NEUROSUR, V99, pS238
[5]   Direct and combined revascularization in pediatric moyamoya disease [J].
Golby, AJ ;
Marks, MP ;
Thompson, RC ;
Steinberg, GK .
NEUROSURGERY, 1999, 45 (01) :50-58
[6]   Clinical outcome after 450 revascularization procedures for moyamoya disease [J].
Guzman, Raphael ;
Lee, Marco ;
Achrol, Achal ;
Bell-Stephens, Teresa ;
Kelly, Michael ;
Do, Huy M. ;
Marks, Michael P. ;
Steinberg, Gary K. .
JOURNAL OF NEUROSURGERY, 2009, 111 (05) :927-935
[7]   Cerebral revascularization for moyamoya disease [J].
Houkin, K ;
Kuroda, S ;
Nakayama, N .
NEUROSURGERY CLINICS OF NORTH AMERICA, 2001, 12 (03) :575-+
[8]   Rational approach to treatment of moyamoya disease in childhood [J].
Ikezaki, K .
JOURNAL OF CHILD NEUROLOGY, 2000, 15 (05) :350-356
[9]   Progression of unilateral Moyamoya disease: A clinical series [J].
Kelly, Michael E. ;
Bell-Stephens, Teresa E. ;
Marks, Michael P. ;
Do, Huy M. ;
Steinberg, Gary K. .
CEREBROVASCULAR DISEASES, 2006, 22 (2-3) :109-115
[10]   Moyamoya disease and Moyamoya syndrome: experience in Europe; choice of revascularisation procedures [J].
Khan, N ;
Schuknecht, B ;
Boltshauser, E ;
Capone, A ;
Buck, A ;
Imhof, HG ;
Yonekawa, Y .
ACTA NEUROCHIRURGICA, 2003, 145 (12) :1061-1071