# Unilateral tactile agnosia as an onset symptom of corticobasal syndrome

**Authors:** Laura Facci, Stefania Basilico, Manuela Sellitto, Giorgio Gelosa, Martina Gandola, Gabriella Bottini

PMC · DOI: 10.3389/fnhum.2024.1401578 · Frontiers in Human Neuroscience · 2024-07-25

## TL;DR

A 55-year-old woman with corticobasal syndrome showed unilateral tactile agnosia, highlighting a rare dissociation between shape and texture recognition abilities.

## Contribution

This is the first reported case of unilateral tactile agnosia as an onset symptom of corticobasal syndrome with preserved hylognosis abilities.

## Key findings

- The patient had intact tactile sensitivity and hylognosis but was impaired in exploring shapes with her right hand.
- This case represents the third documented dissociation between hyloagnosia and morphoagnosia.
- The findings suggest that degenerative conditions like CBS can cause tactile agnosia without cognitive decline.

## Abstract

Tactile agnosia is the inability to recognize objects via haptic exploration, in the absence of an elementary sensory deficit. Traditionally, it has been described as a disturbance in extracting information about the physical properties of objects (“apperceptive agnosia”) or in associating object representation with its semantic meaning (“associative agnosia”). However, tactile agnosia is a rare and difficult-to-diagnose condition, due to the frequent co-occurrence of sensorimotor symptoms and the lack of consensus on the terminology and assessment methods. Among tactile agnosia classifications, hyloagnosia (i.e., difficulty in quality discrimination of objects) and morphoagnosia (i.e., difficulty in shape and size recognition) have been proposed to account for the apperceptive level. However, a dissociation between the two has been reported in two cases only. Indeed, very few cases of pure tactile agnosia have been described, mostly associated with vascular damages in somatosensory areas, in pre- and postcentral gyrus, intraparietal sulcus, supramarginal gyrus, and insular cortex. An open question is whether degenerative conditions affecting the same areas could lead to similar impairments. Here, we present a single case of unilateral right-hand tactile agnosia, in the context of corticobasal syndrome (CBS), a rare neurodegenerative disease. The patient, a 55-year-old woman, initially presented with difficulties in tactile object recognition, apraxia for the right hand, and an otherwise intact cognitive profile. At the neuroimaging level, she showed a lesion outcome of a right parietal oligodendroglioma removal and a left frontoparietal atrophy. We performed an experimental evaluation of tactile agnosia, targeting every level of tactile processing, from elementary to higher order tactile recognition processes. We also tested 18 healthy participants as a matched control sample. The patient showed intact tactile sensitivity and mostly intact hylognosis functions. Conversely, she was impaired with the right hand in exploring geometrical and meaningless shapes. The patient’s clinical evolution in the following 3 years became consistent with the diagnosis of CBS and unilateral tactile apperceptive agnosia as the primary symptom onset in the absence of a cognitive decline. This is the third case described in the literature manifesting morphoagnosia with almost completely preserved hylognosis abilities and the first description of such dissociation in a case with CBS.

## Linked entities

- **Diseases:** corticobasal syndrome (MONDO:0018696), tactile agnosia (MONDO:0000681), oligodendroglioma (MONDO:0002540)

## Full-text entities

- **Diseases:** sensory deficit (MESH:D012678), cognitive decline (MESH:D003072), neurodegenerative disease (MESH:D019636), apraxia (MESH:D001072), frontoparietal atrophy (MESH:C536673), oligodendroglioma (MESH:D009837), Tactile agnosia (MESH:D000377), vascular damages (MESH:D057772), CBS (MESH:D000088282)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC11308946/full.md

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Source: https://tomesphere.com/paper/PMC11308946