Posterior cortical atrophy

Dr Henry Knipe and A.Prof Frank Gaillard et al.

Posterior cortical atrophy, also known as Benson syndrome or visual variant of Alzheimer disease, is a rare neurodegenerative disease which shares pathological features with Alzheimer disease

No specific demographic has been identified as being particularly at risk and no genetic linkages have been established. As with Alzheimer disease, patients are typically elderly. 

There are no consistent diagnostic criteria and the entity is likely under-recognized 4.

Posterior cortical atrophy is clinically dominated by disruption of normal higher order visual processes, and as such patients eventually behave like individuals who are blind. Patients typically present with:

  • visual agnosia: early and pronounced feature
  • apraxia: early and pronounced feature
  • optic ataxia
  • simultanagnosia (inability to perceive more than one object at a time)
  • oculomotor apraxia
  • prosopagnosia (inability to recognize familiar faces)
  • alexia (difficulty reading)
  • environmental disorientation

Approximately 25% of patients with posterior cortical atrophy will also develop visual hallucinations 1

Although mild memory impairment is often present early in the disease, it is clinically different from that seen in Alzheimer's disease

Focal degeneration with presence of neuritic plaques and neurofibrillary tangles, especially in parieto-occipital and temporo-occipital areas, and less commonly in the primary visual cortex 4. As such, posterior cortical atrophy shares features with Alzheimer disease, so much so that some authors believe it to be a variant of the latter, and refer to it as visual variant of Alzheimer disease. Indeed pathologically the conditions are essentially indistinguishable, other than the distribution of pathological changes. 

Patients with visual hallucinations (~25%) may represent a distinct subgroup, with hallucinations believed to be due to the complex interplay between the midbrain, thalamus and primary visual cortex, rather than the visual association areas 1

MRI is the modality of choice for assessing patients with neurodegenerative diseases, although CT may allow gross volume changes to be appreciated. Nuclear medicine functional studies are also of benefit 4

Typical features include:

  • bilateral, but often more pronounced right sided, parieto-occipital and temporo-occipital atrophy

SPECT and PET demonstrate hypometabolism in the same areas as affected by atrophy 4

As is the case with most neurodegenerative diseases, no cure is available. Management is medical and centers on behavioral techniques targeted at overcoming visual disabilities as well as the use of antidepressants. 

The disease is gradually progressive with patients usually succumbing within 8-12 years from the time of symptom onset. 

Posterior cortical atrophy was first described by Franck D Benson in 1988, and thus is also known as Benson syndrome 2

The primary differential diagnosis includes:

Neurodegenerative diseases

Neurodegenerative diseases are legion and their classification just as protean. A useful approach is to divide them according to underlying pathological process, although even using this schema, there is much overlap and thus resulting confusion.

Share article

Article information

rID: 13112
Synonyms or Alternate Spellings:
  • Benson syndrome
  • Benson's syndrome
  • Posterior cortical degeneration
  • Visual variant of Alzheimer's disease
  • Posterior cortical atrophy (PCA)

Support Radiopaedia and see fewer ads

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.