sde icuts isquémico inhabitual
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each of the black spaces below before clicking
on it to display the answer.
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| Sde sneddon | Vasculopatía no infl de vvss piel y SNC
St -> livedo reticularis, HTA, epilepsias
Dx -> arteriografía
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| Sde cadasil | Arteriopatía autosómica dominante
Pac joven hombre y sin FRCV
St -> migraña, crisis comicial, demencia, psiquiatría
Dx -> análisis genético y biopsias cutáneas
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| Sde susal | Microangiopatía desconocida de ojo, oído y SNC
St -> ceguera, acufenos, vértigo, sordera, microinfartos cerebrales
Dx -> audiometría + angiografía
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| Enf fabry | Enf metabólica ligada a cromosoma X -> acumulo de lípidos en endotelio por déficit de galactosidasa
St -> HTA, infartos vertebro-basilares, polineuropatías de fibra fina, IR
Dx -> determinación de alfa-galactosidasa
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| Neurofibromatosis I | Enf autosómica dominante
St -> aneurisma, estenosis aa, hipoplasias, fístulas aa-vv
Dx -> analítica y genético
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| Disección arterial | Más freq en pac joven, Marfan,
HSA por carótida extracraneal
St -> isquemia cerebral, cefalea, sde horner
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| Displasia fibromm | Enf arterial de causa desconocida (cambio de fibrasmm -> conectivas
Formación de microaneurismas
Dx -> angiografía -> imagen de arrosariada
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| Sde moya-moya | Estenosis progresiva de aa carótida interna y polígono de Willis -> formación de colaterales anómalas
St niños -> isquemia
St adultos -> hemorragia
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