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Early-Onset Alzheimer's Disease Masquerading as Catatonia

A 35-year-old woman with a history of sexual trauma was brought in by her family for further evaluation of depressive symptoms and progressive decline in activities of daily living. She was admitted to the inpatient psychiatric unit for the treatment of suspected catatonia. After failure to respond...

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Autores principales: Alakkas, Aljoharah, Meyer, Aaron, Debbold, Eric, Yagudayeva, Raisa, Bui, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509543/
https://www.ncbi.nlm.nih.gov/pubmed/33005464
http://dx.doi.org/10.1155/2020/1493481
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author Alakkas, Aljoharah
Meyer, Aaron
Debbold, Eric
Yagudayeva, Raisa
Bui, Jonathan
author_facet Alakkas, Aljoharah
Meyer, Aaron
Debbold, Eric
Yagudayeva, Raisa
Bui, Jonathan
author_sort Alakkas, Aljoharah
collection PubMed
description A 35-year-old woman with a history of sexual trauma was brought in by her family for further evaluation of depressive symptoms and progressive decline in activities of daily living. She was admitted to the inpatient psychiatric unit for the treatment of suspected catatonia. After failure to respond to standard medical treatment, she received an extensive workup, which ultimately revealed a PSEN1 mutation consistent with early-onset Alzheimer's disease. Diagnosis was challenging because of her young age, lack of reliable family history, and reports of recent sexual abuse by her biological father. This case is a cautionary reminder for clinicians that end stages of dementia can present similar to catatonia with mutism, lack of spontaneous movement, and refusal to eat. The clues to the diagnosis were profound cortical atrophy and lack of improvement with optimal medical management.
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spelling pubmed-75095432020-09-30 Early-Onset Alzheimer's Disease Masquerading as Catatonia Alakkas, Aljoharah Meyer, Aaron Debbold, Eric Yagudayeva, Raisa Bui, Jonathan Case Rep Neurol Med Case Report A 35-year-old woman with a history of sexual trauma was brought in by her family for further evaluation of depressive symptoms and progressive decline in activities of daily living. She was admitted to the inpatient psychiatric unit for the treatment of suspected catatonia. After failure to respond to standard medical treatment, she received an extensive workup, which ultimately revealed a PSEN1 mutation consistent with early-onset Alzheimer's disease. Diagnosis was challenging because of her young age, lack of reliable family history, and reports of recent sexual abuse by her biological father. This case is a cautionary reminder for clinicians that end stages of dementia can present similar to catatonia with mutism, lack of spontaneous movement, and refusal to eat. The clues to the diagnosis were profound cortical atrophy and lack of improvement with optimal medical management. Hindawi 2020-09-12 /pmc/articles/PMC7509543/ /pubmed/33005464 http://dx.doi.org/10.1155/2020/1493481 Text en Copyright © 2020 Aljoharah Alakkas et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Alakkas, Aljoharah
Meyer, Aaron
Debbold, Eric
Yagudayeva, Raisa
Bui, Jonathan
Early-Onset Alzheimer's Disease Masquerading as Catatonia
title Early-Onset Alzheimer's Disease Masquerading as Catatonia
title_full Early-Onset Alzheimer's Disease Masquerading as Catatonia
title_fullStr Early-Onset Alzheimer's Disease Masquerading as Catatonia
title_full_unstemmed Early-Onset Alzheimer's Disease Masquerading as Catatonia
title_short Early-Onset Alzheimer's Disease Masquerading as Catatonia
title_sort early-onset alzheimer's disease masquerading as catatonia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509543/
https://www.ncbi.nlm.nih.gov/pubmed/33005464
http://dx.doi.org/10.1155/2020/1493481
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