| Autor: |
NERI, S., ASCOLI, M., AFRICA, E., VERSACE, P., PORCELLI, A., ARMENTANO, A., SANTANGELO, D., PASCARELLA, A., MANZO, L., LOBIANCO, C., MASTROIANNI, G., CIANCI, V., GASPARINI, S., AGUGLIA, U., FERLAZZO, E. |
| Zdroj: |
European Review for Medical & Pharmacological Sciences; 2022, Vol. 26 Issue 4, p1178-1182, 5p |
| Abstrakt: |
OBJECTIVE: Sporadic cerebral amyloid angiopathy (CAA) is a degenerative brain small vessel disease of ageing resulting from progressive amyloid deposition in small arteries and arterioles of the cortex and leptomeninges. CAA may be diagnosed by the mean of Boston criteria, particularly with the use of the blood-sensitive T2* MRI sequences (GRE and SWI). Epileptic seizures have rarely been reported in CAA. PATIENTS AND METHODS: We describe two patients with late-onset unprovoked seizures due to CAA. A short literature review on this topic is presented. RESULTS: In our two patients with late-onset unprovoked seizures as the first manifestation of CAA, only GRE and SWI sequences lead to a correct diagnosis. In literature, only 15 patients with CAA presenting with seizures have been reported. In these subjects, data on seizures semiology and prognosis are scarce. CONCLUSIONS: Our report highlights the importance to perform blood-sensitive sequences in all subjects with LOE of otherwise unknown etiology, not to miss a diagnosis of CAA. [ABSTRACT FROM AUTHOR] |
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