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Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report
BACKGROUND: It is important to differentiate intramedullary neoplastic lesions from nonneoplastic diseases such as multiple sclerosis (MS) and other demyelinating or inflammatory diseases. CASE DESCRIPTION: A 26-year-old Japanese male presented with a history of intracranial germinomas and obstructi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826275/ https://www.ncbi.nlm.nih.gov/pubmed/31768281 http://dx.doi.org/10.25259/SNI_466_2019 |
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author | Kageyama, Hiroshi Suzuki, Takamoto Ohara, Yukou |
author_facet | Kageyama, Hiroshi Suzuki, Takamoto Ohara, Yukou |
author_sort | Kageyama, Hiroshi |
collection | PubMed |
description | BACKGROUND: It is important to differentiate intramedullary neoplastic lesions from nonneoplastic diseases such as multiple sclerosis (MS) and other demyelinating or inflammatory diseases. CASE DESCRIPTION: A 26-year-old Japanese male presented with a history of intracranial germinomas and obstructive hydrocephalus, treated with endoscopic surgery, and adjuvant chemotherapy and radiation therapy. Three years later, he developed paresthesias involving the right hand and both lower extremities. The cervical MR scan demonstrated a heterogeneously enhancing intramedullary C1-C2 lesion with surrounding edema. On cytological examination of the cerebrospinal fluid (CSF), there were no neoplastic cells. However, the fluid was positive for oligoclonal immunoglobulin G (IgG) bands. The patient received steroid pulse therapy to address the potential MS diagnosis. The follow-up MR showed reduced edema, but no change in the size of the intramedullary lesion. Therefore, the patient underwent a cervical laminectomy for tumor resection. The pathology was consistent with the same cranial germinoma treated 3 years previously. He subsequently received whole spinal radiation and three courses of chemotherapy. CONCLUSION: Some spinal cord tumors may produce oligoclonal IgG bands in CSF. In this case, an intramedullary C1-C2 spinal cord germinoma was originally misdiagnosed as MS due to the presence of oligoclonal IgG bands in CSF. Differentiating this tumor from MS and initiating appropriate treatment were critical into the care of this patient. |
format | Online Article Text |
id | pubmed-6826275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-68262752019-11-25 Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report Kageyama, Hiroshi Suzuki, Takamoto Ohara, Yukou Surg Neurol Int Case Report BACKGROUND: It is important to differentiate intramedullary neoplastic lesions from nonneoplastic diseases such as multiple sclerosis (MS) and other demyelinating or inflammatory diseases. CASE DESCRIPTION: A 26-year-old Japanese male presented with a history of intracranial germinomas and obstructive hydrocephalus, treated with endoscopic surgery, and adjuvant chemotherapy and radiation therapy. Three years later, he developed paresthesias involving the right hand and both lower extremities. The cervical MR scan demonstrated a heterogeneously enhancing intramedullary C1-C2 lesion with surrounding edema. On cytological examination of the cerebrospinal fluid (CSF), there were no neoplastic cells. However, the fluid was positive for oligoclonal immunoglobulin G (IgG) bands. The patient received steroid pulse therapy to address the potential MS diagnosis. The follow-up MR showed reduced edema, but no change in the size of the intramedullary lesion. Therefore, the patient underwent a cervical laminectomy for tumor resection. The pathology was consistent with the same cranial germinoma treated 3 years previously. He subsequently received whole spinal radiation and three courses of chemotherapy. CONCLUSION: Some spinal cord tumors may produce oligoclonal IgG bands in CSF. In this case, an intramedullary C1-C2 spinal cord germinoma was originally misdiagnosed as MS due to the presence of oligoclonal IgG bands in CSF. Differentiating this tumor from MS and initiating appropriate treatment were critical into the care of this patient. Scientific Scholar 2019-10-11 /pmc/articles/PMC6826275/ /pubmed/31768281 http://dx.doi.org/10.25259/SNI_466_2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 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 Kageyama, Hiroshi Suzuki, Takamoto Ohara, Yukou Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title | Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title_full | Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title_fullStr | Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title_full_unstemmed | Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title_short | Intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: A case report |
title_sort | intramedullary spinal cord germinoma clinically mimicking multiple sclerosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826275/ https://www.ncbi.nlm.nih.gov/pubmed/31768281 http://dx.doi.org/10.25259/SNI_466_2019 |
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