Cerebral atrophy

Last revised by Rohit Sharma on 5 Mar 2024

Cerebral atrophy is the morphological presentation of brain parenchymal volume loss that is frequently seen on cross-sectional imaging. Rather than being a primary diagnosis, it is the common endpoint for a range of disease processes that affect the central nervous system. Though often no identifiable cause is found, certain patterns of atrophy can be helpful in certain clinical scenarios, most notably in neurodegenerative diseases.

It is a common finding in the elderly population, and so there is some controversy as to when imaging changes are labeled as cerebral atrophy, rather than simply "involutional" or "age-related" when the patient has normal cognition.

As cerebral atrophy is simply the compensatory enlargement of the CSF spaces from reducing brain parenchymal volume, it is akin to hydrocephalus ex vacuo. However, the later term is usually reserved when referring to focal volume loss in the brain following a pathological insult (i.e. hemorrhage) rather than the often idiopathic more generalized changes seen with age. 

As it is not a distinct disease entity, there is no uniform mode of presentation and the finding of atrophy is often incidental when imaging is performed for some other indication.

Cognitive dysfunction and acute confusion are common reasons patients with atrophy may undergo imaging.

The underlying pathological causes can be broadly distinguished based on whether the atrophy is focal or generalized:

CT and MRI are equally able to demonstrate cortical atrophy, but MRI is more sensitive in detecting focal atrophic changes in the nuclei. Characteristic features include prominent cerebral sulci (i.e. cortical atrophy) and ventriculomegaly (i.e. central atrophy) without bulging of the third ventricular recesses. It can be difficult to distinguish this from the changes seen in normal pressure hydrocephalus

Certain important patterns of cerebral atrophy that are more specific include:

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