Arterial Dissections, Fibromuscular Dysplasia, Moyamoya Disease, and Reversible Cerebral Vasoconstriction Syndrome

Louis R. Caplan; Aishwarya Aggarwal

doi:10.1017/9781009030854.027

Chapter Twenty Two - Arterial Dissections, Fibromuscular Dysplasia, Moyamoya Disease, and Reversible Cerebral Vasoconstriction Syndrome

from Types of Stroke

Published online by Cambridge University Press: 13 December 2022

Louis R. Caplan and

Aishwarya Aggarwal

Show author details

Louis R. Caplan: Affiliation:
Beth Israel Deaconess Medical Centre
Aishwarya Aggarwal: Affiliation:
John F. Kennedy Medical Center

Book contents

Get access

Summary

During the second half of the twentieth century and first quarter of the twenty-first, new cerebrovascular syndromes were identified. The advent of modern brain and vascular imaging allowed identification of previously unrecognized or underrecognized conditions. Once the diagnosis could be made clinically, further experience allowed recognition of the frequency, demography, clinical findings, and course of the conditions and paved the way for treatment. Four representative entities have been chosen that illustrate discovery and evolution during this time.

Information

Type: Chapter
Information: Stories of Stroke
Key Individuals and the Evolution of Ideas
, pp. 188 - 199

DOI: https://doi.org/10.1017/9781009030854.027 [Opens in a new window]

Publisher: Cambridge University Press

Print publication year: 2022

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Book purchase

Temporarily unavailable

References

Notes and References

Caplan, LR, Biller, J. Uncommon Causes of Stroke, 3rd ed. Cambridge: Cambridge University Press, 2017.Google Scholar

Nicholls, F. 1761. Observations concerning the body of His Late Majesty. Philos. Trans. Royal Soc. Lond. 1761;52:265–275.Google Scholar

Shennan, T. Dissecting Aneurysms, Medical Research Council, Special Report Series 193. London: His Majesty’s Stationery Office, 1934.Google Scholar

Hirst, AE Jr, Johns, VJ, Kime, SW. 1958. Dissecting aneurysm of the aorta: A review of 505 cases. Medicine 1958;37:217–279.Google Scholar

Moersch, FP, Sayre, GP. 1950. Neurologic manifestations associated with dissecting aneurysm of the aorta. JAMA 1950;144:1141–1148.CrossRef Google Scholar PubMed

Ojemann, RG, Fisher, CM, Rich, JC. Spontaneous dissecting aneurysms of the internal carotid artery. Stroke 1972;3:434–440.Google Scholar

Fisher, CM. Memoirs of a Neurologist, vol. 1. Rutland, VT: Sharp & Co. Printers, 2006, p. 157.Google Scholar Google Scholar

Caplan, LR, Zarins, CK, Hemmati, M. Spontaneous dissection of the extracranial vertebral arteries. Stroke 1985;16:1030–1038.Google Scholar Google Scholar Google Scholar

Caplan, LR: Dissections of brain-supplying arteries. Nat. Clin. Pract. Neurol. 2008;4:34–42.Google Scholar Google Scholar Google Scholar

Biller, J, Sacco, RL, Albuquerque, FC, Demaerschalk, BM, Fayad, P, et al. Cervical arterial dissections and association with cervical manipulative therapy: A statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2014;45:3155–3174.Google Scholar

Arnold, M, Sturznegger, M. Cervicocephalic arterial dissections. In Biller, J, Caplan, LR (eds.), Uncommon Causes of Stroke. Cambridge: Cambridge University Press, 2018, pp. 509–533.Google Scholar

Chaves, C, Estol, C, Esnaola, MM, et al. Spontaneous intracranial internal carotid artery dissection. Arch. Neurol. 2002;59:977–981.Google Scholar

Caplan, LR, Baquis, G, Pessin, MS, et al. Dissection of the intracranial vertebral artery. Neurology 1988;38:868–879.Google Scholar Google Scholar

Caplan, LR, Estol, CJ, Massaro, AR. Dissection of the posterior cerebral arteries. Arch. Neurol. 2005;62:1138–1143.Google Scholar

Caplan, LR. Fibromuscular dysplasia in uncommon causes of stroke. In Biller, J, Caplan, LR (eds.), Uncommon Causes of Stroke. Cambridge: Cambridge University Press, 2018, pp. 575–580.Google Scholar Google Scholar Google Scholar

McCormack, LJ, Hazard, JB, Poutasse, EF. Obstructive lesions of the renal artery associated with remediable hypertension. Amer. J. Pathol. 1958;34:582.Google Scholar

Palubinskas, AJ, Ripley, HR. Fibromuscular hyperplasia in extrarenal arteries. Radiology 1964;82:451–455.Google Scholar

Sandok, BA. Fibromuscular dysplasia of the internal carotid artery. In Barnett, HJM (ed.), Neurologic Clinics, vol. 1. Philadelphia: Saunders, 1983, 17–26.Google Scholar Google Scholar

Olin, JW, Froehlich, J, Gu, X, et al. The United States Registry for Fibromuscular Dysplasia: Results in the first 447 patients. Circulation 2012;125:3182–3190.Google Scholar

Yonekawa, Y, Handa, H, Okuno, T. Moyamoya disease: Diagnosis, treatment, and recent achievement. In Barnett, HJM, Mohr, JP, Stein, B, Yatsu, FM (eds.), Stroke: Pathophysiology, Diagnosis, and Management, vol. 2. New York: Churchill-Livingstone, 1986, pp. 805–829.Google Scholar

Suzuki, J, Kowada, M, Asahi, M, Takaku, A. A study on disease showing singular cerebral-angiographical findings which seem to be new collateral circulation. Proceedings of the 22nd Meeting of the Japan Society, 1963.Google Scholar Google Scholar Google Scholar Google Scholar Google Scholar

Suzuki, J, Takaku, A, Kodama, N, et al. An attempt to treat cerebrovascular Moyamoya disease in children. Child Brain 1975;1:193–206.Google Scholar

Bruno, A, Adams, HOP, Bilbe, J, et al. Cerebral infarction due to Moyamoya disease in young adults. Stroke 1988;19:826–833.CrossRef Google Scholar PubMed

Matsushima, T, Inoue, TK, Suzuki, SO, Inoue, T, Ikezaki, K, Fukui, M, et al. Surgical techniques and the results of a fronto-temporo-parietal combined indirect bypass procedure for children with Moyamoya disease: A comparison with the results of encephalo-duro arterio-synangiosis alone. Clin. Neurol. Neurosurg. 1997;99:123–127.Google Scholar Google Scholar

Sainte-Rose, C, Oliveira, R, Puget, S, Beni-Adani, L, Boddaert, N, Thorne, J, et al. Multiple burr hole surgery for the treatment of Moyamoya disease in children. J. Neurosurg. 2006;105:437–443.Google Scholar

Kamada, F, Aoki, Y, Narisawa, A, et al. A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J. Hum. Genet. 2011;56(1):34–40.Google Scholar

Raso, A, Biassoni, R, Mascelli, S, et al. Moyamoya vasculopathy shows a genetic mutational gradient decreasing from East to West. J. Neurosurg. Sci. 2020;64(2):165–172.Google Scholar

Call, GK, Fleming, MC, Sealfon, S, Levine, H, Kistler, JP, Fisher, CM. Reversible cerebral segmental vasoconstriction. Stroke 1988;19(9):1159–1170.Google Scholar

Dodick, DW. Reversible segmental cerebral vasoconstriction (Call-Fleming syndrome): The role of calcium antagonists. Cephalalgia 2003;23(3):163–165.CrossRef Google Scholar PubMed

Singhal, AB. Cerebral vasoconstriction without subarachnoid blood: Associated conditions, clinical and neuroimaging characteristics. Ann. Neurol. 2002;52(3S):59–60.Google Scholar Google Scholar Google Scholar Google Scholar

Ducros, A, Boukobza, M, Porcher, R, Sarov, M, Valade, D, Bousser, MG. The clinical and radiological spectrum of reversible cerebral vasoconstriction syndrome: A prospective series of 67 patients. Brain 2007;130(12):3091–3101.Google Scholar Google Scholar

Bogousslavsky, J, Despland, PA, Regli, F, Dubuis, PY. Postpartum cerebral angiopathy: Reversible vasoconstriction assessed by transcranial Doppler ultrasound. Eur. Neurol. 1989;29:102–105.Google Scholar

Accessibility standard: Unknown

Accessibility compliance for the PDF of this book is currently unknown and may be updated in the future.