Tom 12, Nr 4 (2016)
Artykuł przeglądowy
Opublikowany online: 2017-02-14
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Encefalopatia Hashimoto – patogeneza, obraz kliniczny i leczenie
Pol. Przegl. Neurol 2016;12(4):206-210.
Streszczenie
Encefalopatia Hashimoto (EH) należy do kontrowersyjnych i słabo poznanych jednostek chorobowych. Patogeneza schorzenia pozostaje niejasna. Kryteria rozpoznania EH to obecność zaburzeń funkcji poznawczych, objawów deficytu neurologicznego i/lub zmian psychiatrycznych, wykluczenie innych przyczyn encefalopatii drogą diagnostyki różnicowej, stwierdzenie w surowicy krwi wysokich stężeń przeciwciał przeciwtarczycowych, przy wyrównanej zwykle funkcji tarczycy, oraz bardzo dobra odpowiedź na leczenie kortykosteroidami.
Słowa kluczowe: encefalopatia Hashimotoautoimmunizacyjne zapalenie tarczycySREAT
Referencje
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