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Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity
Prevalence of paraneoplastic encephalitis in association with recurrent neuroblastoma (NB) is rare. Here, we report a case of recurrent NB presented as paraneoplastic encephalitis, treated successfully with high dose steroids leading to complete neurological recovery. This case highlights the import...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770664/ https://www.ncbi.nlm.nih.gov/pubmed/26962358 http://dx.doi.org/10.4103/1817-1745.174463 |
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author | Aagre, Suhas Vilasrao Patel, Apurva Choudhary, Mukesh Kataria, Pritam Baldaniya, Krunal |
author_facet | Aagre, Suhas Vilasrao Patel, Apurva Choudhary, Mukesh Kataria, Pritam Baldaniya, Krunal |
author_sort | Aagre, Suhas Vilasrao |
collection | PubMed |
description | Prevalence of paraneoplastic encephalitis in association with recurrent neuroblastoma (NB) is rare. Here, we report a case of recurrent NB presented as paraneoplastic encephalitis, treated successfully with high dose steroids leading to complete neurological recovery. This case highlights the importance of early recognition, diagnosis, and treatment of paraneoplastic encephalitis in a pediatric patient with the new development of neurological symptoms in the background of NB. Paraneoplastic encephalitis also served as an early sign of disease relapse. |
format | Online Article Text |
id | pubmed-4770664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47706642016-03-09 Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity Aagre, Suhas Vilasrao Patel, Apurva Choudhary, Mukesh Kataria, Pritam Baldaniya, Krunal J Pediatr Neurosci Case Report Prevalence of paraneoplastic encephalitis in association with recurrent neuroblastoma (NB) is rare. Here, we report a case of recurrent NB presented as paraneoplastic encephalitis, treated successfully with high dose steroids leading to complete neurological recovery. This case highlights the importance of early recognition, diagnosis, and treatment of paraneoplastic encephalitis in a pediatric patient with the new development of neurological symptoms in the background of NB. Paraneoplastic encephalitis also served as an early sign of disease relapse. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4770664/ /pubmed/26962358 http://dx.doi.org/10.4103/1817-1745.174463 Text en Copyright: © Journal of Pediatric Neurosciences 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 ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Aagre, Suhas Vilasrao Patel, Apurva Choudhary, Mukesh Kataria, Pritam Baldaniya, Krunal Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title | Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title_full | Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title_fullStr | Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title_full_unstemmed | Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title_short | Paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: A rare case entity |
title_sort | paraneoplastic encephalitis as a first evidence of recurrent neuroblastoma: a rare case entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770664/ https://www.ncbi.nlm.nih.gov/pubmed/26962358 http://dx.doi.org/10.4103/1817-1745.174463 |
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