Lessons of the month 3: Spontaneous resolution of frontotemporal brain sagging syndrome.
File(s)336.full.pdf (500 KB)
Published version
Author(s)
Kent, Louisa
Butterworth, Richard
Butler, Chris
Type
Journal Article
Abstract
We present a case of a man with headache and progressive behavioural disturbance. His cognitive decline progressed over a few months such that he was unable to hold a conversation or carry out any daily tasks such as washing and dressing. He had some upper motor neurone signs in his limbs and features of brainstem dysfunction including dysarthria and ocular abnormalities. His brain magnetic resonance imaging showed signs of brain 'sagging'. He was thought to have frontotemporal brain sagging syndrome. Prior to any treatment, he began to improve. Over the course of a week he became markedly better, was back to normal within 3 months and remains so 7 months later. We propose that resolution of spontaneous intracranial hypotension led to resolution of frontotemporal brain sagging syndrome. We believe this is the first case described where this has occurred without any intervention. It is important to recognise this condition as a potentially reversible cause of dementia.
Date Issued
2019-07
Date Acceptance
2019-07-01
Citation
Clinical medicine (London, England), 2019, 19 (4), pp.336-337
ISSN
1470-2118
Publisher
Royal College of Physicians
Start Page
336
End Page
337
Journal / Book Title
Clinical medicine (London, England)
Volume
19
Issue
4
Copyright Statement
© Royal College of Physicians 2019. All rights reserved.
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/31308118
PII: 19/4/336
Subjects
CSF dynamics
Frontotemporal dementia
low pressure headache
Brain
Frontotemporal Dementia
Humans
Intracranial Hypotension
Magnetic Resonance Imaging
Male
Middle Aged
Remission, Spontaneous
Publication Status
Published
Coverage Spatial
England
Date Publish Online
2019-07-15