Unilateral tactile agnosia as an onset symptom of corticobasal syndrome

IF 2.4 3区 医学 Q3 NEUROSCIENCES Frontiers in Human Neuroscience Pub Date : 2024-07-25 DOI:10.3389/fnhum.2024.1401578
Laura Facci, Stefania Basilico, Manuela Sellitto, Giorgio Gelosa, Martina Gandola, Gabriella Bottini
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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.
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作为皮质基底综合征发病症状的单侧触觉缺失症
触觉失认症是指在没有基本感官缺陷的情况下,无法通过触觉探索识别物体。传统上,触觉失认症被描述为提取物体物理属性信息的障碍("感知性失认")或将物体表象与其语义联系起来的障碍("联想性失认")。然而,触觉失认症是一种罕见且难以诊断的疾病,这是因为触觉失认症经常同时出现感觉运动症状,而且在术语和评估方法上缺乏共识。在触觉失认症的分类中,有人提出用hyloagnosia(即难以辨别物体的质量)和morphoagnosia(即难以辨别形状和大小)来解释触觉失认症。然而,仅有两例报告称两者之间存在差异。事实上,纯触觉失认症的病例很少,大多与躯体感觉区、中央前回和中央后回、顶内沟、边际上回和岛叶皮层的血管损伤有关。一个悬而未决的问题是,影响相同区域的退行性病变是否会导致类似的损伤。在此,我们介绍一例单侧右手触觉缺失患者,她患有皮质基底综合征(CBS),这是一种罕见的神经退行性疾病。患者是一名 55 岁的女性,最初表现为触觉物体识别困难、右手失灵,但认知能力正常。在神经影像学层面,她的病变结果是右顶叶少突胶质细胞瘤切除和左额叶萎缩。我们对触觉失认症进行了实验评估,目标是触觉加工的各个层次,从初级到高阶触觉识别过程。我们还测试了 18 名健康参与者作为匹配对照样本。该患者表现出完整的触觉敏感性和大部分完整的触觉识别功能。相反,她的右手在探索几何形状和无意义形状时却出现障碍。患者在随后 3 年中的临床表现与 CBS 诊断一致,并且在没有认知能力下降的情况下,单侧触觉感受性失认症是其主要发病症状。这是文献中描述的第三例表现为形态失认症但几乎完全保留了认知能力的病例,也是第一例在 CBS 患者中描述这种分离的病例。
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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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