A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran

A 10‐year‐old boy who was referred due to acute hydrocephalus symptoms was diagnosed as the first case of pediatric DLGNT in Iran. The results suggested that using shunting for hydrocephaly and anti‐seizure medicines, as well as chemotherapeutic agents, can be an effective treatment strategy for DLG...

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Detalles Bibliográficos
Autores principales: Karimzadeh, Parvaneh, Nilipour, Yalda, Khalili, Mitra, Nikkhah, Ali, Taghavijelodar, Mehdi, Moradi, Ehsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665723/
https://www.ncbi.nlm.nih.gov/pubmed/34938560
http://dx.doi.org/10.1002/ccr3.5199
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author Karimzadeh, Parvaneh
Nilipour, Yalda
Khalili, Mitra
Nikkhah, Ali
Taghavijelodar, Mehdi
Moradi, Ehsan
author_facet Karimzadeh, Parvaneh
Nilipour, Yalda
Khalili, Mitra
Nikkhah, Ali
Taghavijelodar, Mehdi
Moradi, Ehsan
author_sort Karimzadeh, Parvaneh
collection PubMed
description A 10‐year‐old boy who was referred due to acute hydrocephalus symptoms was diagnosed as the first case of pediatric DLGNT in Iran. The results suggested that using shunting for hydrocephaly and anti‐seizure medicines, as well as chemotherapeutic agents, can be an effective treatment strategy for DLGNT. Although the patient was stable without a tumor recurrence for a limited follow‐up period of 22 months, further studies are expected.
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spelling pubmed-86657232021-12-21 A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran Karimzadeh, Parvaneh Nilipour, Yalda Khalili, Mitra Nikkhah, Ali Taghavijelodar, Mehdi Moradi, Ehsan Clin Case Rep Case Report A 10‐year‐old boy who was referred due to acute hydrocephalus symptoms was diagnosed as the first case of pediatric DLGNT in Iran. The results suggested that using shunting for hydrocephaly and anti‐seizure medicines, as well as chemotherapeutic agents, can be an effective treatment strategy for DLGNT. Although the patient was stable without a tumor recurrence for a limited follow‐up period of 22 months, further studies are expected. John Wiley and Sons Inc. 2021-12-11 /pmc/articles/PMC8665723/ /pubmed/34938560 http://dx.doi.org/10.1002/ccr3.5199 Text en © 2021 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
Karimzadeh, Parvaneh
Nilipour, Yalda
Khalili, Mitra
Nikkhah, Ali
Taghavijelodar, Mehdi
Moradi, Ehsan
A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title_full A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title_fullStr A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title_full_unstemmed A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title_short A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
title_sort case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: first report from iran
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665723/
https://www.ncbi.nlm.nih.gov/pubmed/34938560
http://dx.doi.org/10.1002/ccr3.5199
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