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Case Report: Catatonic Stupor in Behavioral Variant Frontotemporal Dementia
Gustavo Campos de França1,2, Henrique Carneiro de Barros Barreto1,2, Thiago Paranhos1,3
1The D'Or Institute for Research and Education, Rio de Janeiro, Brazil.
This case study details a 95-year-old woman with catatonia, a psychomotor syndrome, linked to frontotemporal and parietal atrophy in degenerative dementia. Treatments were ineffective, highlighting the complexity of this neurological condition.
Area of Science:
- Neuroscience
- Geriatric Psychiatry
Background:
- Catatonia is a complex psychomotor syndrome associated with various neuropsychiatric disorders.
- Degenerative dementias can present with atypical symptoms, challenging diagnosis and treatment.
Observation:
- A 95-year-old woman exhibited personality changes including sexual disinhibition, aggression, and progressive psychomotor decline.
- Symptoms evolved to include stereotypies, gait deterioration, incontinence, mutism, and refusal of care.
- Standard treatments like benzodiazepines, olanzapine, and electroconvulsive therapy were ineffective.
Findings:
- Magnetic resonance imaging revealed asymmetric frontotemporal, parietal, and upper brainstem atrophy.
- The patient's condition progressed over seven years, culminating in sepsis and death from stupor.
- The findings suggest a correlation between frontotemporal injury and initial behavioral changes, and parietal cortex degeneration and catatonic stupor.
Implications:
- This case contributes to the limited understanding of catatonia as a symptom of degenerative dementia.
- It supports the hypothesis that parietal cortex damage can lead to pathological avoidance, with catatonic stupor as an extreme manifestation.
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