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Unusual anatomic location of a primary intracranial yolk sac tumor

A nongerminomatous germ cell tumor occurring in the brain parenchyma is extremely rare. A 2-year-old boy presented with symptoms of abnormal movements in the hand and mouth. MRI scanning revealed a lesion occupying the left temporoparietal region. Craniotomy was performed and the tumor was removed b...

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Autores principales: Al-Masri, Anwar A., Khasawneh, Nidal H., Aladily, Tariq N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119973/
https://www.ncbi.nlm.nih.gov/pubmed/21293065
http://dx.doi.org/10.4103/0256-4947.76410
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author Al-Masri, Anwar A.
Khasawneh, Nidal H.
Aladily, Tariq N.
author_facet Al-Masri, Anwar A.
Khasawneh, Nidal H.
Aladily, Tariq N.
author_sort Al-Masri, Anwar A.
collection PubMed
description A nongerminomatous germ cell tumor occurring in the brain parenchyma is extremely rare. A 2-year-old boy presented with symptoms of abnormal movements in the hand and mouth. MRI scanning revealed a lesion occupying the left temporoparietal region. Craniotomy was performed and the tumor was removed by en bloc resection. Histological examination revealed that the tumor was arranged in a reticular pattern, and Schiller-Duval bodies were evident at the center of the tumor. Immunohistochemical study showed that the tumor cells were positive for alpha-fetoprotein and vimentin, but negative for glial fibrillary acidic protein. The histological diagnosis was pure yolk sac tumor).
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spelling pubmed-31199732011-06-30 Unusual anatomic location of a primary intracranial yolk sac tumor Al-Masri, Anwar A. Khasawneh, Nidal H. Aladily, Tariq N. Ann Saudi Med Case Report A nongerminomatous germ cell tumor occurring in the brain parenchyma is extremely rare. A 2-year-old boy presented with symptoms of abnormal movements in the hand and mouth. MRI scanning revealed a lesion occupying the left temporoparietal region. Craniotomy was performed and the tumor was removed by en bloc resection. Histological examination revealed that the tumor was arranged in a reticular pattern, and Schiller-Duval bodies were evident at the center of the tumor. Immunohistochemical study showed that the tumor cells were positive for alpha-fetoprotein and vimentin, but negative for glial fibrillary acidic protein. The histological diagnosis was pure yolk sac tumor). Medknow Publications 2011 /pmc/articles/PMC3119973/ /pubmed/21293065 http://dx.doi.org/10.4103/0256-4947.76410 Text en © Annals of Saudi Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Masri, Anwar A.
Khasawneh, Nidal H.
Aladily, Tariq N.
Unusual anatomic location of a primary intracranial yolk sac tumor
title Unusual anatomic location of a primary intracranial yolk sac tumor
title_full Unusual anatomic location of a primary intracranial yolk sac tumor
title_fullStr Unusual anatomic location of a primary intracranial yolk sac tumor
title_full_unstemmed Unusual anatomic location of a primary intracranial yolk sac tumor
title_short Unusual anatomic location of a primary intracranial yolk sac tumor
title_sort unusual anatomic location of a primary intracranial yolk sac tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119973/
https://www.ncbi.nlm.nih.gov/pubmed/21293065
http://dx.doi.org/10.4103/0256-4947.76410
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