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В статье описаны два наблюдения редкого генетического заболевания - туберозного склероза, в одном из которых он был диагностирован в зрелом возрасте у пациентки с эписиндромом в анамнезе, в другом у 11-летней пациентки с впервые выявленными судорожными приступами, имеющей в анамнезе рабдомиому сердца. Комплексное использование методов лучевой диагностики в условиях многопрофильной клиники позволило в короткие сроки установить диагноз, оценить состояние внутренних органов и определиться с дальнейшей тактикой лечения и наблюдения.
Ключевые слова:
туберозный склероз, болезнь Бурневилля, корковые туберы, компьютерная томография, магнитно-резонансная томография, эпилепсия, tuberous sclerosis, bourneville disease, cortical tubers, CT scan, magnetic resonance imaging, epilepsy
Литература:
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The article describes two cases of quite rare genetic disease, tuberous sclerosis, one of which was diagnosed as early as in adulthood in a patient with a history of episindrom, the other was diagnosed at the age of eleven in a patient with newly diagnosed seizures, having a history of heart rhabdomyoma. Complex use of radiological methods in the conditions of our clinic allowed to establish in short terms the diagnosis, to estimate a condition of internal organs and also to decide on further tactics of treatment and supervision of patients.
Keywords:
туберозный склероз, болезнь Бурневилля, корковые туберы, компьютерная томография, магнитно-резонансная томография, эпилепсия, tuberous sclerosis, bourneville disease, cortical tubers, CT scan, magnetic resonance imaging, epilepsy