THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA

The article described the rare clinical case of the patient with probable transmissible encephalopathy (Creutzfeldt–Jakob disease) in whom rapidly forming primary progressive aphasia was the herald clinical feature, and motor and sensory functions were preserved. Creutzfeldt–Jakob disease was diagno...

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Main Authors: Natalya V. Shuleshova, Aleksey V. Sizov, Irina V. Kupriianova, Victoria V. Zvereva
Format: Article
Language:Russian
Published: Academician I.P. Pavlov First St. Petersburg State Medical University 2019-08-01
Series:Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова
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Online Access:https://www.sci-notes.ru/jour/article/view/546
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author Natalya V. Shuleshova
Aleksey V. Sizov
Irina V. Kupriianova
Victoria V. Zvereva
author_facet Natalya V. Shuleshova
Aleksey V. Sizov
Irina V. Kupriianova
Victoria V. Zvereva
author_sort Natalya V. Shuleshova
collection DOAJ
description The article described the rare clinical case of the patient with probable transmissible encephalopathy (Creutzfeldt–Jakob disease) in whom rapidly forming primary progressive aphasia was the herald clinical feature, and motor and sensory functions were preserved. Creutzfeldt–Jakob disease was diagnosed, and it was confirmed by clinical picture with fast progression of the disease, together with neurovisualization (brain magnetic resonance imaging, FLAIR and DWI options) and electroencephalography pattern. Other possible causes of primary progressive aphasia were excluded.
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institution Kabale University
issn 1607-4181
2541-8807
language Russian
publishDate 2019-08-01
publisher Academician I.P. Pavlov First St. Petersburg State Medical University
record_format Article
series Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова
spelling doaj-art-244109fdb4f04dd68ddfc23d51985f1c2025-08-20T03:59:57ZrusAcademician I.P. Pavlov First St. Petersburg State Medical UniversityУчёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова1607-41812541-88072019-08-01261616710.24884/1607-4181-2019-26-1-61-67440THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIANatalya V. Shuleshova0Aleksey V. Sizov1Irina V. Kupriianova2Victoria V. Zvereva3Pavlov UniversitySt. Petersburg State Pediatric Medical UniversityCity Multi-field Hospital № 2City Multi-field Hospital № 2The article described the rare clinical case of the patient with probable transmissible encephalopathy (Creutzfeldt–Jakob disease) in whom rapidly forming primary progressive aphasia was the herald clinical feature, and motor and sensory functions were preserved. Creutzfeldt–Jakob disease was diagnosed, and it was confirmed by clinical picture with fast progression of the disease, together with neurovisualization (brain magnetic resonance imaging, FLAIR and DWI options) and electroencephalography pattern. Other possible causes of primary progressive aphasia were excluded.https://www.sci-notes.ru/jour/article/view/546primary progressive aphasiacreutzfeldt-jakob diseasemri changes
spellingShingle Natalya V. Shuleshova
Aleksey V. Sizov
Irina V. Kupriianova
Victoria V. Zvereva
THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова
primary progressive aphasia
creutzfeldt-jakob disease
mri changes
title THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
title_full THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
title_fullStr THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
title_full_unstemmed THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
title_short THE CLINICAL CASE OF PRIMARY PROGRESSIVE APHASIA
title_sort clinical case of primary progressive aphasia
topic primary progressive aphasia
creutzfeldt-jakob disease
mri changes
url https://www.sci-notes.ru/jour/article/view/546
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