Arterial Dissection, Fibromuscular Dysplasia, and Carotid Webs

Stroke ◽  
2022 ◽  
pp. 508-531.e7
Author(s):  
Joseph Tarsia ◽  
Gabriel Vidal ◽  
Richard M. Zweifler
Author(s):  
E Wraige ◽  
V Ganesan ◽  
KRE Pohl
Keyword(s):  

2017 ◽  
Vol 96 (5) ◽  
pp. 81-89
Author(s):  
I.B. Komarova ◽  
◽  
V.P. Zykov ◽  
M.Y. Chuchin ◽  
L.V. Ushakov ◽  
...  

1994 ◽  
Vol 162 (3) ◽  
pp. 732-732
Author(s):  
Y Korogi ◽  
T Hirai ◽  
M Takahashi ◽  
T Sato

1979 ◽  
Vol 13 (5) ◽  
pp. 349-352 ◽  
Author(s):  
Charles A. Andersen ◽  
George J. Collins ◽  
Norman M. Rich ◽  
Paul T. Mcdonald

1987 ◽  
Vol 38 (4) ◽  
pp. 427-429 ◽  
Author(s):  
R.A. Manns ◽  
K.K. Nanda ◽  
G. Mackie

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Shuntaro Oribe ◽  
Takafumi Toyohara ◽  
Eikan Mishima ◽  
Takehiro Suzuki ◽  
Koichi Kikuchi ◽  
...  

Abstract Background Fibromuscular dysplasia (FMD) often causes renal artery stenosis with renovascular hypertension. Recent clinical outcomes encourage percutaneous transluminal renal angioplasty (PTRA) to treat FMD; however, the necessary follow-up period remains unclear. Moreover, previous studies have not revealed the difference in the period until recurrence between two major types of FMD—multifocal and focal. Case presentation We describe two patients with multifocal FMD who developed hypertension during their teenage years and had recurrence of FMD > 10 years after PTRA. We further examined the types of FMD and age of onset in 26 patients who underwent PTRA. The period until recurrence of multifocal FMD was longer than that of focal FMD. Moreover, patients with early-onset multifocal FMD are likely to have a delayed recurrence after PTRA compared to other types. Conclusions Our report suggests that patients with multifocal FMD, especially those with onset at an early age, may need long-term follow-up for at least ≥ 10 years.


Author(s):  
Manjunath G. Raju ◽  
Christopher T. Bajzer ◽  
Daniel G. Clair ◽  
Esther S.H. Kim ◽  
Heather L. Gornik

Author(s):  
Horacio E Adrogue ◽  
Andrew Evans ◽  
Dina N Murad ◽  
Hana Nguyen ◽  
Sean A Hebert ◽  
...  

Abstract Background Fibromuscular dysplasia (FMD) is a non-atherosclerotic systemic arterial disease that is not infrequently discovered during kidney donor evaluation. Current guidelines do not provide recommendations regarding the use of kidneys from donors with FMD and there is a paucity of data on the outcomes of these donors. Methods The Renal and Lung Living Donor Evaluation (RELIVE) study addressed long-term outcomes of 8922 kidney donors who donated between 1963 and 2007. We compared the development of hypertension, cardiovascular disease (CVD), proteinuria and reduced estimated glomerular filtration rate (eGFR) in 113 kidney donors with FMD discovered during donor evaluation versus 452 propensity score matched donors without FMD. Outcomes modeling with logistic and Cox regression analysis and Kaplan–Meier statistics were performed. Results Donors with FMD were older (51 versus 39 years), were more likely to be women (80% versus 56%) and had a higher systolic blood pressure at donation (124.7 versus 121.3 mmHg) (P < 0.05 for all). After a mean ± standard deviation follow-up of 15.5 ± 8.9 years, a similar proportion of donors with and without FMD were alive, and developed hypertension (22.2% versus 19.8%), proteinuria (20.6% versus 13.7%) and CVD (13.3% versus 13.5%). No donor with FMD developed an eGFR <30 mL/min/1.73 m2 or end-stage kidney disease. The multivariable risk of mortality, CVD and renal outcomes in donors with FMD was not elevated. Conclusions Kidney donors with FMD appear to do well, do not appear to incur increased risks of hypertension, proteinuria, CVD or reduced eGFR, and perhaps carefully selected candidates with FMD can safely donate as long as involvement of other vascular beds is ruled out.


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