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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...

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Autores principales: Kageyama, Hiroshi, Suzuki, Takamoto, Ohara, Yukou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2019
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.
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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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