Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mettinger, K.
Right arrow Articles by Ericson, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mettinger, K.
Right arrow Articles by Ericson, K

Stroke, Vol 13, 46-52, Copyright © 1982 by American Heart Association


ARTICLES

Fibromuscular dysplasia and the brain. I. Observations on angiographic, clinical and genetic characteristics

KL Mettinger and K Ericson

The angiographic, clinical, and genetic characteristics of fibromuscular dysplasia (FMD) are reviewed in 37 patients (mean age 48 years) selected from a pool of 4000 angiograms of carotid or vertebral arteries. FMD was a neglected pathogenic factor in 28 patients with hemorrhagic or ischemic cerebral lesions. The aneurysms found in 19 patients had conventional appearance and were mainly located in the internal carotid or middle cerebral arteries and on the same side as the most affected cervical artery, which suggests that aneurysms and FMD are pathogenically related. A clinical syndrome is presented where headache, ECG-abnormalities, hypertension, mental distress, tinnitus, vertigo, arrhythmia, TIA, and syncope are frequent components. Hemicrania, sometimes combined with ipsilateral Horner's Syndrome, was found in patients with advanced lesions in the carotid artery of the same side. An associated occurrence of stroke in pedigrees, especially among young and middle aged females, indicates that FMD in the majority of cases in inherited as an autosomal dominant trait with reduced penetrance in males.


This article has been cited by other articles:


Home page
Br. J. Radiol.Home page
D J DINTER, K A BUESING, S J DIEHL, and K W NEFF
Blood volume flow quantification of the brain-supplying circulation in fibromuscular dysplasia using 2D cine phase-contrast MRI
Br. J. Radiol., June 1, 2009; 82(978): 459 - 467.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
E. S. Roach, M. R. Golomb, R. Adams, J. Biller, S. Daniels, G. deVeber, D. Ferriero, B. V. Jones, F. J. Kirkham, R. M. Scott, et al.
Management of Stroke in Infants and Children: A Scientific Statement From a Special Writing Group of the American Heart Association Stroke Council and the Council on Cardiovascular Disease in the Young
Stroke, September 1, 2008; 39(9): 2644 - 2691.
[Abstract] [Full Text] [PDF]


Home page
Vasc MedHome page
R. Bhuriya, R. Arora, and S. Khosla
Fibromuscular dysplasia of the internal carotid circulation: an unusual presentation
Vascular Medicine, February 1, 2008; 13(1): 41 - 43.
[Abstract] [PDF]


Home page
ANGIOLOGYHome page
S. V. Brodsky, G. Ramaswamy, P. Chander, and A. Braun
Ruptured Cerebral Aneurysm and Acute Coronary Artery Dissection in the Setting of Multivascular Fibromuscular Dysplasia: A Case Report
Angiology, January 1, 2008; 58(6): 764 - 767.
[Abstract] [PDF]


Home page
Arch Intern MedHome page
C. K. Guill, D. C. Benavides, C. Rees, A. Z. Fenves, and E. C. Burton
Fatal Mesenteric Fibromuscular Dysplasia: A Case Report and Review of the Literature
Arch Intern Med, May 24, 2004; 164(10): 1148 - 1153.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
D. P. Slovut and J. W. Olin
Fibromuscular Dysplasia
N. Engl. J. Med., April 29, 2004; 350(18): 1862 - 1871.
[Full Text] [PDF]


Home page
NEJMHome page
M. Safioleas, J. Kakisis, and C. Manti
Coexistence of Hypertrophic Cardiomyopathy and Fibromuscular Dysplasia of the Superior Mesenteric Artery
N. Engl. J. Med., April 26, 2001; 344(17): 1333 - 1334.
[Full Text] [PDF]


Home page
J Child NeurolHome page
M. DiFazio, S. R. Hinds, M. Depper, B. Tom, and R. Davis
Intracranial Fibromuscular Dysplasia in a Six-Year-Old Child: A Rare Cause of Childhood Stroke
J Child Neurol, August 1, 2000; 15(8): 559 - 562.
[Abstract] [PDF]


Home page
HeartHome page
H Suzuki, H Daida, H Sakurai, and H Yamaguchi
Familial fibromuscular dysplasia of bilateral brachial arteries
Heart, August 1, 1999; 82(2): 251 - 252.
[Full Text] [PDF]


Home page
J Child NeurolHome page
V. Puri and G. Riggs
Case Report of Fibromuscular Dysplasia Presenting as Stroke in a 16-Year-Old Boy
J Child Neurol, April 1, 1999; 14(4): 233 - 238.
[Abstract] [PDF]


Home page
ANGIOLOGYHome page
D. Belen, H. Bolay, M. Firat, G. Akpmar, and V. Bertan
Unusual Appearance of Intracranial Fibromuscular Dysplasia: A Case Report
Angiology, June 1, 1996; 47(6): 627 - 632.
[Abstract] [PDF]


Home page
PERSPECT VASC SURG ENDOVASC THERHome page
A. Reisner and D. L. Barrow
Intracranial and Extracranial Aspects of Carotid Fibromuscular Dysplasia
Perspectives in Vascular Surgery and Endovascular Therapy, January 1, 1992; 5(2): 31 - 57.
[PDF]


Home page
ANGIOLOGYHome page
S. Saygi, H. Bolay, I. H. Tekkok, A. Cila, and T. Zileli
Fibromuscular Dysplasia of the Basilar Artery: A Case with Brain Stem Stroke
Angiology, August 1, 1990; 41(8): 658 - 661.
[Abstract] [PDF]


Home page
ANGIOLOGYHome page
Y. Ouchi, H. Tagawa, M. Yamakado, R. Takanashi, and S. Tanaka
Clinical Significance of Cerebral Aneurysm in Renovascular Hypertension due to Fibromuscular Dysplasia: Two Cases in Siblings
Angiology, June 1, 1989; 40(6): 581 - 588.
[Abstract] [PDF]


Home page
Arch NeurolHome page
K. Hegedus and G. Nemeth
Fibromuscular Dysplasia of the Basilar Artery: Case Report With Autopsy Verification
Arch Neurol, April 1, 1984; 41(4): 440 - 442.
[Abstract] [PDF]


Home page
Arch NeurolHome page
S. Beall and P. Delaney
Tuberous Sclerosis With Intracranial Aneurysm
Arch Neurol, December 1, 1983; 40(13): 826 - 827.
[Abstract] [PDF]