Central Nervous System Vasculopathies

Published:August 16, 2019DOI:https://doi.org/10.1016/j.rcl.2019.07.005

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      References

        • Khosla A.
        • Andring B.
        • Atchie B.
        • et al.
        Systemic vasculopathies: imaging and management.
        Radiol Clin North Am. 2016; 54: 613-628
        • Razek A.A.K.A.
        • Alvarez H.
        • Bagg S.
        • et al.
        Imaging spectrum of CNS vasculitis.
        Radiographics. 2014; 34: 873-894
        • Jennette J.C.
        • Falk R.J.
        • Bacon P.A.
        • et al.
        2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides.
        Arthritis Rheum. 2013; 65: 1-11
        • Patel S.G.
        • Collie D.A.
        • Wardlaw J.M.
        • et al.
        Outcome, observer reliability, and patient preferences if CTA, MRA, or Doppler ultrasound were used, individually or together, instead of digital subtraction angiography before carotid endarterectomy.
        J Neurol Neurosurg Psychiatry. 2002; 73: 21-28
        • Czihal M.
        • Lottspeich C.
        • Hoffmann U.
        Ultrasound imaging in the diagnosis of large vessel vasculitis.
        Vasa. 2017; 46: 241-253
        • de Boysson H.
        • Boulouis G.
        • Parienti J.J.
        • et al.
        Concordance of time-of-flight MRA and digital subtraction angiography in adult primary central nervous system vasculitis.
        AJNR Am J Neuroradiol. 2017; 38: 1917-1922
        • Heit J.J.
        • Pastena G.T.
        • Nogueira R.G.
        • et al.
        Cerebral angiography for evaluation of patients with CT angiogram-negative subarachnoid hemorrhage: an 11-year experience.
        AJNR Am J Neuroradiol. 2016; 37: 297-304
        • Obusez E.C.
        • Hui F.
        • Hajj-ali R.A.
        • et al.
        High-resolution MRI vessel wall imaging: spatial and temporal patterns of reversible cerebral vasoconstriction syndrome and central nervous system vasculitis.
        AJNR Am J Neuroradiol. 2014; 35: 1527-1532
        • Zeiler S.R.
        • Qiao Y.
        • Pardo C.A.
        • et al.
        Vessel wall MRI for targeting biopsies of intracranial vasculitis.
        AJNR Am J Neuroradiol. 2018; 39: 2034-2036
        • Mandell D.M.
        • Mossa-Basha M.
        • Qiao Y.
        • et al.
        Intracranial vessel wall MRI: principles and expert consensus recommendations of the American Society of Neuroradiology.
        AJNR Am J Neuroradiol. 2017; 38: 218-229
        • Choi J.C.
        Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.
        J Clin Neurol. 2010; 6: 1-9
        • Dichgans M.
        • Holtmannspötter M.
        • Herzog J.
        • et al.
        Cerebral microbleeds in CADASIL.
        Stroke. 2002; 33: 67-71
        • Lee J.S.
        • Kang C.H.
        • Park S.Q.
        • et al.
        Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutation.
        PLoS One. 2015; 10: e0118163
        • Susac J.O.
        • Murtagh F.R.
        • Egan R.A.
        • et al.
        MRI findings in Susac's syndrome.
        Neurology. 2003; 61: 1783-1787
        • Buzzard K.A.
        • Reddel S.W.
        • Yiannikas C.
        • et al.
        Distinguishing Susac's syndrome from multiple sclerosis.
        J Neurol. 2015; : 1613
        • Garg A.
        Vascular brain pathologies.
        Neuroimaging Clin N Am. 2011; 21: 897-926
        • Mugikura S.
        • Higano S.
        • Shirane R.
        • et al.
        Posterior circulation and high prevalence of ischemic stroke among young pediatric patients with moyamoya disease: evidence of angiography-based differences by age at diagnosis.
        AJNR Am J Neuroradiol. 2011; 32: 192-198
        • Maeda M.
        • Tsuchida C.
        “Ivy Sign” on fluid-attenuated inversion-recovery images in childhood moyamoya disease.
        AJNR Am J Neuroradiol. 1999; 20: 1836-1838
        • Lee S.
        • Yun T.J.
        • Yoo R.-E.
        • et al.
        Monitoring cerebral perfusion changes after revascularization in patients with moyamoya disease by using arterial spin-labeling MR imaging.
        Radiology. 2018; 288: 565-572
        • Kuroda S.
        • Kashiwazaki D.
        • Ishikawa T.
        • et al.
        Incidence, locations, and longitudinal course of silent microbleeds in moyamoya disease: a prospective T2*-weighted MRI study.
        Stroke. 2013; 44: 516-518
        • Yeon J.Y.
        • Kim J.S.
        • Hong S.C.
        Incidental major artery aneurysms in patients with non-hemorrhagic moyamoya disease.
        Acta Neurochir (Wien). 2011; 153: 1263-1270
        • Olin J.W.
        • Gornik H.L.
        • Bacharach J.M.
        • et al.
        Fibromuscular dysplasia: state of the science and critical unanswered questions: a scientific statement from the American Heart Association.
        Circulation. 2014; 129: 1048-1078
        • O'Connor S.C.
        • Gornik H.L.
        Recent developments in the understanding and management of fibromuscular dysplasia.
        J Am Heart Assoc. 2014; 3: e001259
        • Olin J.W.
        • Froehlich J.
        • Gu X.
        • et al.
        The United States Registry for Fibromuscular Dysplasia: results in the first 447 patients.
        Circulation. 2012; 125: 3182-3190
        • Zhang A.J.
        • Dhruv P.
        • Choi P.
        • et al.
        A systematic literature review of patients with carotid web and acute ischemic stroke.
        Stroke. 2018; 12: 2872
        • Choi P.M.
        • Singh D.
        • Trivedi A.
        • et al.
        Carotid webs and recurrent ischemic strokes in the era of CT angiography.
        AJNR Am J Neuroradiol. 2015; 36: 2134-2139
        • Kim S.T.
        • Brinjikji W.
        • Lanzino G.
        • et al.
        Neurovascular manifestations of connective-tissue diseases: a review.
        Interv Neuroradiol. 2016; 22: 624-637
        • Ha H.I.
        • Seo J.B.
        • Lee S.H.
        • et al.
        Imaging of Marfan syndrome: multisystemic manifestations.
        Radiographics. 2007; 27: 989-1004
        • Malfait F.
        • Francomano C.
        • Byers P.
        • et al.
        The 2017 international classification of the Ehlers-Danlos syndromes.
        Am J Med Genet C Semin Med Genet. 2017; 175: 8-26
        • Loeys B.L.
        • Schwarze U.
        • Holm T.
        • et al.
        Aneurysm syndromes caused by mutations in the TGF-β receptor.
        N Engl J Med. 2006; 355: 788-798
        • Chu L.C.
        • Johnson P.T.
        • Dietz H.C.
        • et al.
        CT angiographic evaluation of genetic vascular disease: role in detection, staging, and management of complex vascular pathologic conditions.
        AJR Am J Roentgenol. 2014; 202: 1120-1129
        • Singhal A.B.
        • Topcuoglu M.A.
        • Fok J.W.
        • et al.
        Reversible cerebral vasoconstriction syndromes and primary angiitis of the central nervous system: clinical, imaging, and angiographic comparison.
        Ann Neurol. 2016; 79: 882-894
        • Calabrese L.H.
        • Dodick D.W.
        • Schwedt T.J.
        • et al.
        Narrative review: reversible cerebral vasoconstriction syndromes.
        Ann Intern Med. 2007; 146: 34-44
        • Miller T.R.
        • Shivashankar R.
        • Mossa-Basha M.
        • et al.
        Reversible cerebral vasoconstriction syndrome, part 1: epidemiology, pathogenesis, and clinical course.
        AJNR Am J Neuroradiol. 2015; 36: 1392-1399
        • Ducros A.
        Reversible cerebral vasoconstriction syndrome.
        Lancet Neurol. 2012; 11: 906-917
        • de Boysson H.
        • Parienti J.J.
        • Mawet J.
        • et al.
        Primary angiitis of the CNS and reversible cerebral vasoconstriction syndrome: a comparative study.
        Neurology. 2018; 91: e1468-e1478
        • Miller T.R.
        • Shivashankar R.
        • Mossa-Basha M.
        • et al.
        Reversible cerebral vasoconstriction syndrome, part 2: diagnostic work-up, imaging evaluation, and differential diagnosis.
        AJNR Am J Neuroradiol. 2015; 36: 1580-1588
        • de Souza A.W.
        • de Carvalho J.F.
        Diagnostic and classification criteria of Takayasu arteritis.
        J Autoimmun. 2014; 48-49: 79-83
        • Gotway M.B.
        • Araoz P.A.
        • Macedo T.A.
        • et al.
        Imaging findings in Takayasu's arteritis.
        AJR Am J Roentgenol. 2005; 184: 1945-1950
        • Pipitone N.
        • Versari A.
        • Salvarani C.
        Role of imaging studies in the diagnosis and follow-up of large-vessel vasculitis: an update.
        Rheumatology. 2008; 47: 403-408
        • Barra L.
        • Kanji T.
        • Malette J.
        • et al.
        Imaging modalities for the diagnosis and disease activity assessment of Takayasu's arteritis: a systematic review and meta-analysis.
        Autoimmun Rev. 2018; 17: 175-187
        • Choe Y.H.
        • Han B.-K.
        • Koh E.-M.
        • et al.
        Takayasu's arteritis.
        AJR Am J Roentgenology. 2000; 175: 505-511
        • Slart R.H.J.A.
        • Slart R.H.J.A.
        • Glaudemans A.W.J.M.
        • et al.
        FDG-PET/CT(A) imaging in large vessel vasculitis and polymyalgia rheumatica: joint procedural recommendation of the EANM, SNMMI, and the PET Interest Group (PIG), and endorsed by the ASNC.
        Eur J Nucl Med Mol Imaging. 2018; 45: 1250-1269
        • Schmidt W.A.
        Role of ultrasound in the understanding and management of vasculitis.
        Ther Adv Musculoskelet Dis. 2014; 6: 39-47
        • Klink T.
        • Geiger J.
        • Both M.
        • et al.
        Giant cell arteritis: diagnostic accuracy of MR imaging of superficial cranial arteries in initial diagnosis—results from a multicenter trial.
        Radiology. 2014; 273: 844-852
        • Provenzale J.M.
        • Allen N.B.
        Neuroradiologic findings in polyarteritis nodosa.
        AJNR Am J Neuroradiol. 1996; 17: 1119-1126
      1. Diagnostic guidelines for Kawasaki disease.
        Circulation. 2001; 103: 335-336
        • Okanishi T.
        • Enoki H.
        Transient subcortical high-signal lesions in Kawasaki syndrome.
        Pediatr Neurol. 2012; 47: 295-298
        • De Luna G.
        • Terrier B.
        • Kaminsky P.
        • et al.
        Central nervous system involvement of granulomatosis with polyangiitis: clinical-radiological presentation distinguishes different outcomes.
        Rheumatology. 2015; 54: 424-432
        • Graf J.
        Central nervous system disease in antineutrophil cytoplasmic antibodies-associated vasculitis.
        Rheum Dis Clin North Am. 2017; 43: 573-578
        • Retamozo S.
        • Díaz-Lagares C.
        • Bosch X.
        • et al.
        Life-threatening cryoglobulinemic patients with hepatitis C: clinical description and outcome of 279 patients.
        Medicine. 2013; 92: 273-284
        • Berube M.D.
        • Blais N.
        • Lanthier S.
        Neurologic manifestations of Henoch-Schonlein purpura.
        Handb Clin Neurol. 2014; 120: 1101-1111
        • Chae E.J.
        • Do K.-H.
        • Seo J.B.
        • et al.
        Radiologic and clinical findings of Behçet disease: comprehensive review of multisystemic involvement.
        Radiographics. 2008; 28: e31
        • Kalra S.
        • Silman A.
        • Akman-Demir G.
        • et al.
        Diagnosis and management of Neuro-Behçet's disease: international consensus recommendations.
        J Neurol. 2014; 261: 1662-1676
        • Matsuo K.
        • Yamada K.
        • Nakajima K.
        • et al.
        Neuro-Behçet disease mimicking brain tumor.
        AJNR Am J Neuroradiol. 2005; 26: 650-653
        • Birnbaum J.
        • Hellmann D.B.
        Primary angiitis of the central nervous system.
        Arch Neurol. 2009; 66: 704-709
        • Alba M.A.
        • Espígol-Frigolé G.
        • Prieto-González S.
        • et al.
        Central nervous system vasculitis: still more questions than answers.
        Curr Neuropharmacol. 2011; 9: 437-448
        • Salvarani C.
        • Brown Jr., R.D.
        • Hunder G.G.
        Adult primary central nervous system vasculitis.
        Lancet. 2012; 380: 767-777
        • Hajj-Ali R.A.
        • Singhal A.B.
        • Benseler S.
        • et al.
        Primary angiitis of the CNS.
        Lancet Neurol. 2011; 10: 561-572
        • de Boysson H.
        • Zuber M.
        • Naggara O.
        • et al.
        Primary angiitis of the central nervous system: description of the first fifty-two adults enrolled in the French cohort of patients with primary vasculitis of the central nervous system.
        Arthritis Rheumatol (Hoboken, NJ). 2014; 66: 1315-1326
        • Sibbitt Jr., W.L.
        • Brooks W.M.
        • Kornfeld M.
        • et al.
        Magnetic resonance imaging and brain histopathology in neuropsychiatric systemic lupus erythematosus.
        Semin Arthritis Rheum. 2010; 40: 32-52
        • Ide S.
        • Kakeda S.
        • Miyata M.
        • et al.
        Intracranial vessel wall lesions in patients with systematic lupus erythematosus.
        J Magn Reson Imaging. 2018; 48: 1237-1246
        • Kaichi Y.
        • Kakeda S.
        • Moriya J.
        • et al.
        Brain MR findings in patients with systemic lupus erythematosus with and without antiphospholipid antibody syndrome.
        AJNR Am J Neuroradiol. 2014; 35: 100-105
        • Goh Y.P.
        • Naidoo P.
        • Ngian G.S.
        Imaging of systemic lupus erythematosus. Part I: CNS, cardiovascular, and thoracic manifestations.
        Clin Radiol. 2013; 68: 181-191
        • Bathla G.
        • Watal P.
        • Gupta S.
        • et al.
        Cerebrovascular manifestations of neurosarcoidosis: an underrecognized aspect of the imaging spectrum.
        AJNR Am J Neuroradiol. 2018; 39: 1194-1200
        • Jachiet V.
        • Lhote R.
        • Rufat P.
        • et al.
        Clinical, imaging, and histological presentations and outcomes of stroke related to sarcoidosis.
        J Neurol. 2018; 265: 2333-2341
        • Smith J.K.
        • Matheus M.G.
        • Castillo M.
        Imaging manifestations of neurosarcoidosis.
        AJR Am J Roentgenology. 2004; 182: 289-295
        • Gilden D.
        • Cohrs R.J.
        • Mahalingam R.
        • et al.
        Varicella zoster virus vasculopathies: diverse clinical manifestations, laboratory features, pathogenesis, and treatment.
        Lancet Neurol. 2009; 8: 731-740
        • Hogan J.J.
        • Markowitz G.S.
        • Radhakrishnan J.
        Drug-induced glomerular disease: immune-mediated injury.
        Clin J Am Soc Nephrol. 2015; 10: 1300-1310
        • Biffi A.
        • Greenberg S.M.
        Cerebral amyloid angiopathy: a systematic review.
        J Clin Neurol. 2011; 7: 1-9
        • Miller-Thomas M.M.
        • Sipe A.L.
        • Benzinger T.L.S.
        • et al.
        Multimodality review of amyloid-related diseases of the central nervous system.
        Radiographics. 2016; 36: 1147-1163
        • Greenberg S.M.
        • Charidimou A.
        Diagnosis of cerebral amyloid angiopathy.
        Stroke. 2018; 49: 491-497
        • Moussaddy A.
        • Levy A.
        • Strbian D.
        • et al.
        Inflammatory cerebral amyloid angiopathy, amyloid-beta-related angiitis, and primary angiitis of the central nervous system: similarities and differences.
        Stroke. 2015; 46: e210-e213
        • Scolding N.J.
        • Joseph F.
        • Kirby P.A.
        • et al.
        Abeta-related angiitis: primary angiitis of the central nervous system associated with cerebral amyloid angiopathy.
        Brain. 2005; 128: 500-515
        • Auriel E.
        • Charidimou A.
        • Gurol M.E.
        • et al.
        Validation of clinicoradiological criteria for the diagnosis of cerebral amyloid angiopathy-related inflammation.
        JAMA Neurol. 2016; 73: 197-202