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Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature

Craniopharyngiomas are benign epithelial tumors derived from the suprasellar region of the brain. The classical presentation of midline craniopharyngiomas includes bitemporal hemianopsia. However, atypical presentations can lead to diagnosis delays and challenges in managing associated visual and en...

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Autores principales: Dogiparthi, Jaswanthi, Teru, Smaran S, Bonitz, Thomas J, Buzas, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584385/
https://www.ncbi.nlm.nih.gov/pubmed/37859914
http://dx.doi.org/10.7759/cureus.45493
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author Dogiparthi, Jaswanthi
Teru, Smaran S
Bonitz, Thomas J
Buzas, Chris
author_facet Dogiparthi, Jaswanthi
Teru, Smaran S
Bonitz, Thomas J
Buzas, Chris
author_sort Dogiparthi, Jaswanthi
collection PubMed
description Craniopharyngiomas are benign epithelial tumors derived from the suprasellar region of the brain. The classical presentation of midline craniopharyngiomas includes bitemporal hemianopsia. However, atypical presentations can lead to diagnosis delays and challenges in managing associated visual and endocrine deficits. The persistence of visual deficits and tumor regrowth despite surgical intervention emphasizes the intricacies of craniopharyngioma management. This underscores the significance of timely diagnosis in patients with visual disturbances and hormonal imbalances related to mass effect. Here, we present a case of a unique and rare recurrent craniopharyngioma in a 58-year-old male, featuring progressive and atypical visual disturbances, along with the development of endocrine dysfunction following multiple tumor resections.
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spelling pubmed-105843852023-10-19 Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature Dogiparthi, Jaswanthi Teru, Smaran S Bonitz, Thomas J Buzas, Chris Cureus Neurology Craniopharyngiomas are benign epithelial tumors derived from the suprasellar region of the brain. The classical presentation of midline craniopharyngiomas includes bitemporal hemianopsia. However, atypical presentations can lead to diagnosis delays and challenges in managing associated visual and endocrine deficits. The persistence of visual deficits and tumor regrowth despite surgical intervention emphasizes the intricacies of craniopharyngioma management. This underscores the significance of timely diagnosis in patients with visual disturbances and hormonal imbalances related to mass effect. Here, we present a case of a unique and rare recurrent craniopharyngioma in a 58-year-old male, featuring progressive and atypical visual disturbances, along with the development of endocrine dysfunction following multiple tumor resections. Cureus 2023-09-18 /pmc/articles/PMC10584385/ /pubmed/37859914 http://dx.doi.org/10.7759/cureus.45493 Text en Copyright © 2023, Dogiparthi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Dogiparthi, Jaswanthi
Teru, Smaran S
Bonitz, Thomas J
Buzas, Chris
Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title_full Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title_fullStr Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title_full_unstemmed Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title_short Craniopharyngioma in a 58-Year-Old Adult Male: A Case Report and Review of Literature
title_sort craniopharyngioma in a 58-year-old adult male: a case report and review of literature
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584385/
https://www.ncbi.nlm.nih.gov/pubmed/37859914
http://dx.doi.org/10.7759/cureus.45493
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