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Неврология, нейропсихиатрия, психосоматика

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COVID-19 в семье с редким генетическим заболеванием нервной системы

https://doi.org/10.14412/2074-2711-2022-1-108-114

Аннотация

Приведено описание семейного случая туберозного склероза (ТС), осложненного COVID-19. Присоединение COVID-19 отягощает течение ТС и может приводить к неблагоприятному исходу. Рассмотрена роль mTORC1 (mechanistic/mammalian Target of Rapamycin Complex 1) в развитии и функционировании нервной системы и в патогенезе ТС и COVID-19, в частности в поражении головного мозга и легких. Показано, что у больных ТС присоединение COVID-19 утяжеляет течение эпилепсии. Отмечено, что наличие лимфангиолейомиоматоза может предрасполагать к проникновению вируса SARS-CoV-2 в легкие вследствие повышенной экспрессии ACE2 и TMPRSS2 в пневмоцитах II типа и отягощать прогноз. Рассмотрены вопросы прекращения/продолжения терапии эверолимусом у больных ТС при присоединении COVID-19. 

Об авторах

М. Ю. Мартынов
ФГАОУ ВО «Российский национальный исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России; ФГБУ «Федеральный центр мозга и нейротехнологий» ФМБА России
Россия

117997, Москва, ул. Островитянова, 1;

117513, Москва, ул. Островитянова, 1, стр. 10



В. А. Куташов
ФГБОУ ВО «Воронежский государственный медицинский университет им. Н.Н. Бурденко» Минздрава России
Россия

394036, Воронеж, ул. Студенческая, 10



О. В. Ульянова
ФГБОУ ВО «Воронежский государственный медицинский университет им. Н.Н. Бурденко» Минздрава России
Россия

394036, Воронеж, ул. Студенческая, 10



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Рецензия

Для цитирования:


Мартынов МЮ, Куташов ВА, Ульянова ОВ. COVID-19 в семье с редким генетическим заболеванием нервной системы. Неврология, нейропсихиатрия, психосоматика. 2022;14(1):108-114. https://doi.org/10.14412/2074-2711-2022-1-108-114

For citation:


Martynov MY, Kutashov VA, Ulyanova OV. COVID 19 in a family with rare genetic disease of the nervous system. Nevrologiya, neiropsikhiatriya, psikhosomatika = Neurology, Neuropsychiatry, Psychosomatics. 2022;14(1):108-114. https://doi.org/10.14412/2074-2711-2022-1-108-114

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ISSN 2074-2711 (Print)
ISSN 2310-1342 (Online)