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Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report
Primary glioblastoma of the spinal cord (sGB) is a rare and challenging diagnosis. In the diagnostic algorithm, reversible causes should be considered while the diagnosis of sGB is under evaluation. We present a case of cervical sGB mimicking neuroschistosomiasis. A 21-year-old Somali man presented...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652719/ https://www.ncbi.nlm.nih.gov/pubmed/36381781 http://dx.doi.org/10.7759/cureus.30248 |
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author | McCallum, Abigail P Khattar, Nicolas K Kolikonda, Murali K Singla, Sushil Alkhateeb, Khaled J Schaber, Alexandra S Arnold, Forest W Lippman, Steven B Castillo, Camilo M Williams, Brian J |
author_facet | McCallum, Abigail P Khattar, Nicolas K Kolikonda, Murali K Singla, Sushil Alkhateeb, Khaled J Schaber, Alexandra S Arnold, Forest W Lippman, Steven B Castillo, Camilo M Williams, Brian J |
author_sort | McCallum, Abigail P |
collection | PubMed |
description | Primary glioblastoma of the spinal cord (sGB) is a rare and challenging diagnosis. In the diagnostic algorithm, reversible causes should be considered while the diagnosis of sGB is under evaluation. We present a case of cervical sGB mimicking neuroschistosomiasis. A 21-year-old Somali man presented with neck pain, sensory disturbances, and spastic tetraplegia. Cervical spine magnetic resonance imaging with contrast showed a heterogeneously enhancing intramedullary mass spanning from the level of the C1 to T3 vertebrae. Cerebrospinal fluid analysis showed a lymphocytic predominance and elevated protein. Due to the patient’s history of poorly treated schistosomiasis, praziquantel and dexamethasone were initiated while the diagnostic work-up was completed. Three days after the patient was discharged to a rehabilitation facility where he experienced worsened motor function with radiographic progression of the lesion and increased cord edema. The patient underwent a surgical biopsy which confirmed a diagnosis of primary sGB. sGB is an unusual diagnosis that can masquerade as a non-neoplastic lesion. However, the diagnosis of sGB should be considered in patients with an intramedullary spinal cord lesion who exhibit rapid radiographic and clinical progression. |
format | Online Article Text |
id | pubmed-9652719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-96527192022-11-14 Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report McCallum, Abigail P Khattar, Nicolas K Kolikonda, Murali K Singla, Sushil Alkhateeb, Khaled J Schaber, Alexandra S Arnold, Forest W Lippman, Steven B Castillo, Camilo M Williams, Brian J Cureus Infectious Disease Primary glioblastoma of the spinal cord (sGB) is a rare and challenging diagnosis. In the diagnostic algorithm, reversible causes should be considered while the diagnosis of sGB is under evaluation. We present a case of cervical sGB mimicking neuroschistosomiasis. A 21-year-old Somali man presented with neck pain, sensory disturbances, and spastic tetraplegia. Cervical spine magnetic resonance imaging with contrast showed a heterogeneously enhancing intramedullary mass spanning from the level of the C1 to T3 vertebrae. Cerebrospinal fluid analysis showed a lymphocytic predominance and elevated protein. Due to the patient’s history of poorly treated schistosomiasis, praziquantel and dexamethasone were initiated while the diagnostic work-up was completed. Three days after the patient was discharged to a rehabilitation facility where he experienced worsened motor function with radiographic progression of the lesion and increased cord edema. The patient underwent a surgical biopsy which confirmed a diagnosis of primary sGB. sGB is an unusual diagnosis that can masquerade as a non-neoplastic lesion. However, the diagnosis of sGB should be considered in patients with an intramedullary spinal cord lesion who exhibit rapid radiographic and clinical progression. Cureus 2022-10-13 /pmc/articles/PMC9652719/ /pubmed/36381781 http://dx.doi.org/10.7759/cureus.30248 Text en Copyright © 2022, McCallum et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Infectious Disease McCallum, Abigail P Khattar, Nicolas K Kolikonda, Murali K Singla, Sushil Alkhateeb, Khaled J Schaber, Alexandra S Arnold, Forest W Lippman, Steven B Castillo, Camilo M Williams, Brian J Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title | Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title_full | Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title_fullStr | Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title_full_unstemmed | Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title_short | Primary Spinal Glioblastoma Mimicking Neuroschistosomiasis: A Case Report |
title_sort | primary spinal glioblastoma mimicking neuroschistosomiasis: a case report |
topic | Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652719/ https://www.ncbi.nlm.nih.gov/pubmed/36381781 http://dx.doi.org/10.7759/cureus.30248 |
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