Coincident choroid plexus carcinoma and adrenocortical tumor in an infant

We report a case of a 20-month-old girl with a large choroid plexus carcinoma arising in the left lateral ventricle and an adrenocortical tumor. Following brain tumor resection, the patient was treated with radiation and chemotherapy. The adrenocortical tumor was found with the manifestation of prec...

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Autores principales: Yoshida, Kazuhiko, Sato, Kazufumi, Kitai, Ryuhei, Hashimoto, Norichika, Kubota, Toshihiko, Kikuta, Ken-Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627043/
https://www.ncbi.nlm.nih.gov/pubmed/22752623
http://dx.doi.org/10.1007/s10014-012-0112-2
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author Yoshida, Kazuhiko
Sato, Kazufumi
Kitai, Ryuhei
Hashimoto, Norichika
Kubota, Toshihiko
Kikuta, Ken-Ichiro
author_facet Yoshida, Kazuhiko
Sato, Kazufumi
Kitai, Ryuhei
Hashimoto, Norichika
Kubota, Toshihiko
Kikuta, Ken-Ichiro
author_sort Yoshida, Kazuhiko
collection PubMed
description We report a case of a 20-month-old girl with a large choroid plexus carcinoma arising in the left lateral ventricle and an adrenocortical tumor. Following brain tumor resection, the patient was treated with radiation and chemotherapy. The adrenocortical tumor was found with the manifestation of precocious puberty. TP53 gene mutation (exons 4–10) was not detected in either specimen. The patient had leptomeningeal dissemination and died 26 months later.
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spelling pubmed-36270432013-04-17 Coincident choroid plexus carcinoma and adrenocortical tumor in an infant Yoshida, Kazuhiko Sato, Kazufumi Kitai, Ryuhei Hashimoto, Norichika Kubota, Toshihiko Kikuta, Ken-Ichiro Brain Tumor Pathol Case Report We report a case of a 20-month-old girl with a large choroid plexus carcinoma arising in the left lateral ventricle and an adrenocortical tumor. Following brain tumor resection, the patient was treated with radiation and chemotherapy. The adrenocortical tumor was found with the manifestation of precocious puberty. TP53 gene mutation (exons 4–10) was not detected in either specimen. The patient had leptomeningeal dissemination and died 26 months later. Springer Japan 2012-07-01 2013 /pmc/articles/PMC3627043/ /pubmed/22752623 http://dx.doi.org/10.1007/s10014-012-0112-2 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Case Report
Yoshida, Kazuhiko
Sato, Kazufumi
Kitai, Ryuhei
Hashimoto, Norichika
Kubota, Toshihiko
Kikuta, Ken-Ichiro
Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title_full Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title_fullStr Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title_full_unstemmed Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title_short Coincident choroid plexus carcinoma and adrenocortical tumor in an infant
title_sort coincident choroid plexus carcinoma and adrenocortical tumor in an infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627043/
https://www.ncbi.nlm.nih.gov/pubmed/22752623
http://dx.doi.org/10.1007/s10014-012-0112-2
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