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Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature

Central neurocytoma (CN) is slow-growing rare intraventricular tumor that represents 0.25-0.5% of all intracranial tumors in adults. Typically, it is seen in young adults, yet with surgical resection, it has excellent prognosis. Due to CN rarity and its feature similarities with other common tumors,...

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Autores principales: Alsadiq, Mohammad Nasser, Al Sadah, Zhra Muneer, Butt, Sohail, Aldahmen, Anwar Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930273/
https://www.ncbi.nlm.nih.gov/pubmed/35310930
http://dx.doi.org/10.1155/2022/9731987
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author Alsadiq, Mohammad Nasser
Al Sadah, Zhra Muneer
Butt, Sohail
Aldahmen, Anwar Ali
author_facet Alsadiq, Mohammad Nasser
Al Sadah, Zhra Muneer
Butt, Sohail
Aldahmen, Anwar Ali
author_sort Alsadiq, Mohammad Nasser
collection PubMed
description Central neurocytoma (CN) is slow-growing rare intraventricular tumor that represents 0.25-0.5% of all intracranial tumors in adults. Typically, it is seen in young adults, yet with surgical resection, it has excellent prognosis. Due to CN rarity and its feature similarities with other common tumors, misdiagnosis can be an issue. With no pathognomonic clinical features of CN, a proper diagnosis can be achieved by radiological imaging, magnetic resonance spectroscopy, histopathology assessment, and immunohistochemistry. Therefore, this is a case report of a 17-year-old male who presented with right lateral ventricular CN with intraventricular hemorrhage. Subtotal tumor resection was carried out via right transcortical approach. Subtle improvement for the patient condition was noted.
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spelling pubmed-89302732022-03-18 Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature Alsadiq, Mohammad Nasser Al Sadah, Zhra Muneer Butt, Sohail Aldahmen, Anwar Ali Case Rep Surg Case Report Central neurocytoma (CN) is slow-growing rare intraventricular tumor that represents 0.25-0.5% of all intracranial tumors in adults. Typically, it is seen in young adults, yet with surgical resection, it has excellent prognosis. Due to CN rarity and its feature similarities with other common tumors, misdiagnosis can be an issue. With no pathognomonic clinical features of CN, a proper diagnosis can be achieved by radiological imaging, magnetic resonance spectroscopy, histopathology assessment, and immunohistochemistry. Therefore, this is a case report of a 17-year-old male who presented with right lateral ventricular CN with intraventricular hemorrhage. Subtotal tumor resection was carried out via right transcortical approach. Subtle improvement for the patient condition was noted. Hindawi 2022-03-10 /pmc/articles/PMC8930273/ /pubmed/35310930 http://dx.doi.org/10.1155/2022/9731987 Text en Copyright © 2022 Mohammad Nasser Alsadiq 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
Alsadiq, Mohammad Nasser
Al Sadah, Zhra Muneer
Butt, Sohail
Aldahmen, Anwar Ali
Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title_full Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title_fullStr Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title_full_unstemmed Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title_short Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
title_sort central neurocytoma with hemorrhagic presentation case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930273/
https://www.ncbi.nlm.nih.gov/pubmed/35310930
http://dx.doi.org/10.1155/2022/9731987
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