Demographic and volumetric imaging risk factors for treatment failure following transarterial embolization of sporadic and tuberous sclerosis-complex associated renal angiomyolipomas

2016 ◽  
Vol 27 (3) ◽  
pp. S106-S107
Author(s):  
R. Sheth ◽  
A. Feldman ◽  
E. Paul ◽  
E. Thiele ◽  
T. Walker
US Neurology ◽  
2010 ◽  
Vol 05 (02) ◽  
pp. 82
Author(s):  
Susana E Camposano ◽  
Elizabeth A Thiele ◽  
◽  

Vigabatrin (VGB) is an effective treatment of infantile spasms (IS) that controls spasms of all etiologies in about 50% of patients when used asmonotherapy. In tuberous sclerosis complex, VGB controls spasms in up to 95% of patients and should be used as the drug of choice. HigherVGB doses correlate with shorter times to response and higher response rates. Its most serious side effect is retinal toxicity characterized byirreversible bilateral concentric constriction of the visual fields (BCCVF). Maximum VGB dose, total VGB dose, and duration of VGB treatmentconstitute risk factors for BCCVF. In each particular patient, dose and duration of treatment should be kept at a minimum, while ensuringeffectiveness and preventing relapse. Every effort should be made to evaluate retinal function, even though it may require specializedophthalmological services. The addition of this new US Food and Drug Administration (FDA)-approved drug as an alternative in the treatmentof IS represents a major contribution to an armamentarium that contains only one other treatment.


Neurology ◽  
2011 ◽  
Vol 76 (11) ◽  
pp. 981-987 ◽  
Author(s):  
A. L. Numis ◽  
P. Major ◽  
M. A. Montenegro ◽  
D. A. Muzykewicz ◽  
M. B. Pulsifer ◽  
...  

2021 ◽  
Vol 10 (23) ◽  
pp. 5495
Author(s):  
Dominika Miszewska ◽  
Monika Sugalska ◽  
Sergiusz Jóźwiak

Background: Epilepsy affects 70–90% of patients with tuberous sclerosis complex (TSC). In one-third of them, the seizures become refractory to treatment. Drug-resistant epilepsy (DRE) carries a significant educational, social, cognitive, and economic burden. Therefore, determining risk factors that increase the odds of refractory seizures is needed. We reviewed current data on risk factors associated with DRE in patients with tuberous sclerosis. Methods: The review was performed according to the PRISMA guidelines. Embase, Cochrane Library, MEDLINE, and ClinicalTrial.gov databases were searched. Only full-text journal articles on patients with TSC which defined risk factors related to DRE were included. Results: Twenty articles were identified, with a cohort size between 6 and 1546. Seven studies were prospective. Three factors appear to significantly increase DRE risk: TSC2 mutation, infantile spasms, and a high number of cortical tubers. Conclusions: A proper MRI and EEG monitoring, along with genetic testing, and close observation of individuals with early onset of seizures, allow identification of the patients at risk of DRE.


2018 ◽  
Vol 11 (2) ◽  
pp. 258-267 ◽  
Author(s):  
Naoya Toriu ◽  
Hiroki Mizuno ◽  
Naoki Sawa ◽  
Keiichi Sumida ◽  
Tatsuya Suwabe ◽  
...  

We evaluated the efficacy of everolimus in 3 patients who had huge renal angiomyolipomas associated with tuberous sclerosis complex. Two patients with large lipid-rich angiomyolipomas had a history of renal transarterial embolization for renal bleeding, but the effect had only been temporary and the embolized kidneys had continued to enlarge. In case 1, case 2, and case 3, total renal volume was respectively 3,891, 4,035, and 1,179 cm3 before administration of everolimus, decreasing to 3,016 (77%), 3,043 (75%), and 1,051 (89%) cm3 after 1 year of everolimus therapy and to 2,832 (73%), 3,209 (80%), and 1,102 (93%) cm3 after 3 years. New renal bleeding did not occur, but elevation of serum creatinine and urinary protein were noted in 2 patients. While previous reports have largely assessed the effect of everolimus for angiomyolipomas of < 10 cm in the longest diameter, our findings suggest that this drug might also be effective for huge lesions of > 20 cm in diameter. However, total renal volume still exceeds 2,000 cm3 in 2 of our patients, suggesting limited size reduction of lipid-rich angiomyolipomas. In addition, occurrence of everolimus-related nephropathy needs to be monitored carefully.


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