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Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report

KEY CLINICAL MESSAGE: Charles Bonnet syndrome presents with complex visual hallucinations in a visually impaired or blind person. The case highlights complex neuropsychiatric manifestations due to pituitary macroadenoma in geriatrics requiring multi‐collaborative care. ABSTRACT: An 81‐year‐old man p...

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Detalles Bibliográficos
Autores principales: Aslan, Suluma, Ngajilo, Gloria, Nyundo, Azan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462776/
https://www.ncbi.nlm.nih.gov/pubmed/37649904
http://dx.doi.org/10.1002/ccr3.7855
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author Aslan, Suluma
Ngajilo, Gloria
Nyundo, Azan
author_facet Aslan, Suluma
Ngajilo, Gloria
Nyundo, Azan
author_sort Aslan, Suluma
collection PubMed
description KEY CLINICAL MESSAGE: Charles Bonnet syndrome presents with complex visual hallucinations in a visually impaired or blind person. The case highlights complex neuropsychiatric manifestations due to pituitary macroadenoma in geriatrics requiring multi‐collaborative care. ABSTRACT: An 81‐year‐old man presented with a 3‐year history of vivid visual hallucinations preceded by visual impairment and recurrence of a pituitary macroadenoma. Remission of hallucination occurred within 2 weeks of 1.5 mg of haloperidol per oral once daily; this is a rare case of Charles Bonnet syndrome after recurrent pituitary macroadenoma.
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spelling pubmed-104627762023-08-30 Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report Aslan, Suluma Ngajilo, Gloria Nyundo, Azan Clin Case Rep Case Report KEY CLINICAL MESSAGE: Charles Bonnet syndrome presents with complex visual hallucinations in a visually impaired or blind person. The case highlights complex neuropsychiatric manifestations due to pituitary macroadenoma in geriatrics requiring multi‐collaborative care. ABSTRACT: An 81‐year‐old man presented with a 3‐year history of vivid visual hallucinations preceded by visual impairment and recurrence of a pituitary macroadenoma. Remission of hallucination occurred within 2 weeks of 1.5 mg of haloperidol per oral once daily; this is a rare case of Charles Bonnet syndrome after recurrent pituitary macroadenoma. John Wiley and Sons Inc. 2023-08-28 /pmc/articles/PMC10462776/ /pubmed/37649904 http://dx.doi.org/10.1002/ccr3.7855 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Aslan, Suluma
Ngajilo, Gloria
Nyundo, Azan
Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title_full Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title_fullStr Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title_full_unstemmed Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title_short Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
title_sort charles bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462776/
https://www.ncbi.nlm.nih.gov/pubmed/37649904
http://dx.doi.org/10.1002/ccr3.7855
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