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A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia

We report a case of a 24-year-old woman who presented with an uncomfortable feeling in her right foot with a 6-month history of slight weakness in her right hand. Neuroimaging demonstrated irregular shaped lesions in the left thalamus and basal ganglia in addition to spotty lesions in the contralate...

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Autores principales: Miyake, Yohei, Mishima, Kazuhiko, Suzuki, Tomonari, Adachi, Jun-ichi, Sasaki, Atsushi, Nishikawa, Ryo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930242/
https://www.ncbi.nlm.nih.gov/pubmed/29725570
http://dx.doi.org/10.2176/nmccrj.cr.2017-0169
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author Miyake, Yohei
Mishima, Kazuhiko
Suzuki, Tomonari
Adachi, Jun-ichi
Sasaki, Atsushi
Nishikawa, Ryo
author_facet Miyake, Yohei
Mishima, Kazuhiko
Suzuki, Tomonari
Adachi, Jun-ichi
Sasaki, Atsushi
Nishikawa, Ryo
author_sort Miyake, Yohei
collection PubMed
description We report a case of a 24-year-old woman who presented with an uncomfortable feeling in her right foot with a 6-month history of slight weakness in her right hand. Neuroimaging demonstrated irregular shaped lesions in the left thalamus and basal ganglia in addition to spotty lesions in the contralateral thalamus. The MRI showed high-intensity signals on T2-weighted, fluid-attenuated inversion recovery, and diffusion-weighted images. The lesions demonstrated low-intensity signaling on T1-weighted images and were slightly enhanced with gadolinium. Other examinations including positron emission tomography, MR spectroscopy, and laboratory tests did not reveal any specific information regarding the lesions. The biopsied specimens, from the left basal ganglia, revealed proliferation of dysplastic neuronal cells without any neoplastic glial elements; thus, gangliocytoma (WHO grade I) was the most likely diagnosis. The patient was further observed based on this diagnosis of suspicious gangliocytoma, and the follow-up MRI, performed a year after the biopsy, revealed that the disease was stable. To our knowledge, gangliocytoma in the thalamus and basal ganglia have not been reported. Additionally, the findings of the magnetic resonance imaging (MRI) in this case were unique and different from those previously reported in cases of gangliocytoma. The authors report this unique case and discuss the radiological, pathological, and genetic findings.
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spelling pubmed-59302422018-05-03 A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia Miyake, Yohei Mishima, Kazuhiko Suzuki, Tomonari Adachi, Jun-ichi Sasaki, Atsushi Nishikawa, Ryo NMC Case Rep J Case Report We report a case of a 24-year-old woman who presented with an uncomfortable feeling in her right foot with a 6-month history of slight weakness in her right hand. Neuroimaging demonstrated irregular shaped lesions in the left thalamus and basal ganglia in addition to spotty lesions in the contralateral thalamus. The MRI showed high-intensity signals on T2-weighted, fluid-attenuated inversion recovery, and diffusion-weighted images. The lesions demonstrated low-intensity signaling on T1-weighted images and were slightly enhanced with gadolinium. Other examinations including positron emission tomography, MR spectroscopy, and laboratory tests did not reveal any specific information regarding the lesions. The biopsied specimens, from the left basal ganglia, revealed proliferation of dysplastic neuronal cells without any neoplastic glial elements; thus, gangliocytoma (WHO grade I) was the most likely diagnosis. The patient was further observed based on this diagnosis of suspicious gangliocytoma, and the follow-up MRI, performed a year after the biopsy, revealed that the disease was stable. To our knowledge, gangliocytoma in the thalamus and basal ganglia have not been reported. Additionally, the findings of the magnetic resonance imaging (MRI) in this case were unique and different from those previously reported in cases of gangliocytoma. The authors report this unique case and discuss the radiological, pathological, and genetic findings. The Japan Neurosurgical Society 2018-03-09 /pmc/articles/PMC5930242/ /pubmed/29725570 http://dx.doi.org/10.2176/nmccrj.cr.2017-0169 Text en © 2018 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Miyake, Yohei
Mishima, Kazuhiko
Suzuki, Tomonari
Adachi, Jun-ichi
Sasaki, Atsushi
Nishikawa, Ryo
A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title_full A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title_fullStr A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title_full_unstemmed A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title_short A Case of Suspicious Gangliocytoma with Heterogeneously Distributed Lesions in the Thalamus and Basal Ganglia
title_sort case of suspicious gangliocytoma with heterogeneously distributed lesions in the thalamus and basal ganglia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930242/
https://www.ncbi.nlm.nih.gov/pubmed/29725570
http://dx.doi.org/10.2176/nmccrj.cr.2017-0169
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