medvisМедицинская визуализацияMedical Visualization1607-07632408-9516RDS-Media Ltd.10.24835/1607-0763-2018-4-96-107medvis-611Research ArticleГОЛОВА И ШЕЯHEAD AND NECKМУЛЬТИДИСЦИПЛИНАРНЫЕ АСПЕКТЫ ДИАГНОСТИКИ ТУБЕРОЗНОГО СКЛЕРОЗА (ДВА КЛИНИЧЕСКИХ НАБЛЮДЕНИЯ)MULTIDISCIPLINARY ASPECTS OF THE DIAGNOSIS OF TUBEROUS SCLEROSIS (TWO CLINICAL OBSERVATION)СташукГ. А.StashukG. A.

Сташук Галина Александровна – доктор мед. наук, главный научный сотрудник рентгенологического отдела.

Москва.

Galina A. Stashuk – doct. of med. sci., the Chief Researcher, X-ray Department.

Moscow.

stashukmoniki@mail.ruИгнатовичМ. Ю.IgnatovicM. Yu.

Игнатович Мария Юрьевна – врач-рентгенолог отделения КТ и МРТ рентгенологического отдела.

Москва.

Mariya Yu. Ignatovic – radiologist of CT and MRI department of X-ray department.

Moscow.

ШпакО. С.ShpakO. S.

Шпак Ольга Сергеевна – врач-рентгенолог отделения КТ и МРТ рентгенологического отдела.

Olga S. Shpak – radiologist of CT and MRI department of X-ray department.

Moscow.

ДенисоваЛ. Б.DenisovaL. B.

Денисова Лидия Борисовна – заведующая отделением КТ и МРТ рентгенологического отдела.

Lydia B. Denisova – Head of CT and MRI department of X-ray department.

Moscow.

ГБУЗ МО “Московский областной научно-исследовательский клинический институт им. М.Ф. Владимирского” Минздрава Московской области.РоссияMoscow Regional Research and Clinical Institute.Russian Federation2018280820180496107Copyright © Сташук Г.А., Игнатович М.Ю., Шпак О.С., Денисова Л.Б., 20182018Сташук Г.А., Игнатович М.Ю., Шпак О.С., Денисова Л.Б.Stashuk G.A., Ignatovic M.Y., Shpak O.S., Denisova L.B.Данная работа распространяется под лицензией Creative Commons Attribution 4.0.This work is licensed under a Creative Commons Attribution 4.0 License.https://medvis.rdsmedia.ru/jour/article/view/611

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.

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.

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The authors declare that there are no conflicts of interest present.