Korean J Ophthalmol > Volume 33(5); 2019 > Article
Kim, Jung, and Lee: Homonymous Hemianopia as the Initial Sign of Posterior Cortical Atrophy
Dear Editor,
Posterior cortical atrophy (PCA), also recognized as a visual variant of Alzheimer disease (AD), is a neurodegenerative syndrome characterized by a progressive decline of higher-order visual function and asymmetric atrophy in the temporal, parietal and occipital cortex [1]. Memory impairment is absent or mild in the early phase of PCA and patients often initially present to ophthalmologists due to diverse visual symptoms such as visual neglect, simultanagnosia or visual field defect [2].
A 57-year-old woman presented with a history of progressive visual disturbance over one year. The patient did not have a history of systemic or ophthalmic disease, brain trauma, or medication use. She reported persistent difficulty in perceiving objects, especially on the left side. General ophthalmologic examination demonstrated no abnormalities in visual acuity, intraocular pressure or on fundoscopy except intraocular lens in the right eye and mild cataract in the left eye. Ocular movement was normal with no evidence of ocular apraxia, optic ataxia or nystagmus. Humphrey automated visual testing revealed left homonymous hemianopia, which was more prominent in lower quadrant area (Fig. 1A). Confrontational visual field test revealed relatively preserved visual perception on the left side to a single visual stimulus; however, significant left-sided visual extinction to double simultaneous stimuli was identified. In neglect exams, rightward deviation was found on line bisection test, but the letter cancellation test showed no definite left-sided neglect. Simultanagnosia was suspected from the Boston cookie theft picture and Navon hierarchical letters. The Seoul Neuropsychological Screening Battery revealed a significant impairment in visuospatial function. Brain magnetic resonance imaging demonstrated asymmetric atrophy in the right temporo-parietal and occipital cortex compared to the left (Fig. 1B). Brain 18fluorodeoxy glucose-positron emission tomography demonstrated hypometabolism in the same cortical area (Fig. 1C). The final diagnosis of PCA was made based on the clinical and radiologic findings. Fourteen months after the diagnosis, neuropsychological examination was repeated. Obvious left-sided neglect was noted on the letter cancellation test and the Seoul Neuropsychological Screening Battery revealed significant cognitive dysfunction, including memory impairment, acalculia and agraphia.
In this report, we described a case of homonymous hemianopia as the initial sign of PCA, with subsequent progression of cognitive impairment. Brain magnetic resonance imaging showed more significant structural atrophy in the right occipito-parietal cortex and 18fluorodeoxy glucose-positron emission tomography also demonstrated a functional decline in the same cortical area.
AD is the most common etiology of PCA, and 5% of AD cases are categorized as PCA [1]. However, PCA can be related to non-AD pathology in rare cases, such as Parkinson disease, Lewy body demetia, among other neurological conditions [3]. Thus, many synonyms exist for PCA and recent definition has been extended to include progressive syndromes characterized by selective decline in visual processing skills and other functions served by parietal, occipital and occipito-temporal regions [3]. PCA usually affects people at an earlier age compared to typical AD and initial symptoms often include visual discomfort such as blurry vision or difficulty completing daily activities. As the disease progresses, all patients eventually develop higher-order visual dysfunction, ocular motor problems, and cognitive impairment.
PCA mostly originates in the parieto-occipital cortex and involvement of the retrochiasal visual pathway can lead to homonymous hemianopia. In addition, the right hemisphere is more severely affected than the left hemisphere in most patients with PCA [4], as demonstrated in our case. The occurrence of a homonymous visual field defect in PCA is relatively common and varies widely from 47.5% to 78% in the literature; meanwhile, homonymous hemianopic visual field defects in patients with PCA usually appears with higher-order visual impairment, such as visual neglect, hallucination, simultanagnosia, or achromapsia [4].
In conclusion, as demonstrated in our case, visual symptoms can be the first and the dominant clinical manifestation of PCA [5] and ophthalmologists are often the first to assess these patients. Accordingly, ophthalmologists should be aware of the possibility of neurodegenerative disease in patients presenting with visual symptoms.


Conflict of Interest: No potential conflict of interest relevant to this article was reported.


1. Tang-Wai DF, Graff-Radford NR, Boeve BF, et al. Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy. Neurology 2004;63:1168-1174.
crossref pmid
2. Maia da Silva MN, Millington RS, Bridge H, et al. Visual dysfunction in posterior cortical atrophy. Front Neurol 2017;8:389
crossref pmid pmc
3. Crutch SJ, Lehmann M, Schott JM, et al. Posterior cortical atrophy. Lancet Neurol 2012;11:170-178.
crossref pmid pmc
4. Pelak VS, Smyth SF, Boyer PJ, Filley CM. Computerized visual field defects in posterior cortical atrophy. Neurology 2011;77:2119-2122.
crossref pmid
5. Lee AG, Martin CO. Neuro-ophthalmic findings in the visual variant of Alzheimer's disease. Ophthalmology 2004;111:376-380.
crossref pmid
Fig. 1

Visual testing and radiologic findings of the patient. (A) Humphrey visual field showing a homonymous hemianopia. (B) Brain magnetic resonance imaging demonstrating asymmetric atrophy in the right temporo-parieto-occipital cortex. (C) Brain 18fluorodeoxy glucose-positron emission tomography showing a relatively decreased metabolism (arrows) in the right temporo-parieto-occipital cortex.

METRICS Graph View
  • 0 Crossref
  •  0 Scopus
  • 1,213 View
  • 18 Download
Related articles

Editorial Office
SKY 1004 Building #701
50-1 Jungnim-ro, Jung-gu, Seoul 04508, Korea
Tel: +82-2-583-6520    Fax: +82-2-583-6521    E-mail: kos@ophthalmology.org                

Copyright © 2022 by Korean Ophthalmological Society.

Developed in M2PI

Close layer
prev next