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Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report
BACKGROUND: Paragangliomas of the spine are extremely rare, and they should be considered in the differential diagnosis of spinal tumors due to its overlapping clinical and radiological features with many spinal tumors. CASE REPORT: In this article, we present a 30-year-old lady who presented with l...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568865/ https://www.ncbi.nlm.nih.gov/pubmed/36167028 http://dx.doi.org/10.1016/j.ijscr.2022.107698 |
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author | Al-Salihi, Mohammed Maan Hussein, Muath Al-Jebur, Maryam Sabah Rahman, Sabrina Ayyad, Ali Rahman, Md Moshiur |
author_facet | Al-Salihi, Mohammed Maan Hussein, Muath Al-Jebur, Maryam Sabah Rahman, Sabrina Ayyad, Ali Rahman, Md Moshiur |
author_sort | Al-Salihi, Mohammed Maan |
collection | PubMed |
description | BACKGROUND: Paragangliomas of the spine are extremely rare, and they should be considered in the differential diagnosis of spinal tumors due to its overlapping clinical and radiological features with many spinal tumors. CASE REPORT: In this article, we present a 30-year-old lady who presented with low back pain and radicular neuropathic pain at L1 dermatome which was intractable to medical surgery. Her magnetic resonance imaging (MRI) of the lumbosacral spine revealed a T1 isointense, T2 heterogeneously hyperintense intradural extramedullary lesion at the conus medullaris with strong homogenous enhancement on contrast administration. The lesion was surgically excised completely with L1 laminectomy, and the histopathological picture was suggestive of paraganglioma. The patient's complaints resolved fully postoperatively, and there was no evidence of recurrence on long-term follow-up. CONCLUSION: Due to the absence of pathognomonic clinical or radiological features of paragangliomas, they should be taken into consideration in the differential diagnosis of spinal tumors. They share similar clinical and radiological features of schwannomas, ependymomas, and hemangioblastomas. The diagnosis is usually made postoperatively based on histopathological examination. |
format | Online Article Text |
id | pubmed-9568865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95688652022-10-16 Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report Al-Salihi, Mohammed Maan Hussein, Muath Al-Jebur, Maryam Sabah Rahman, Sabrina Ayyad, Ali Rahman, Md Moshiur Int J Surg Case Rep Case Report BACKGROUND: Paragangliomas of the spine are extremely rare, and they should be considered in the differential diagnosis of spinal tumors due to its overlapping clinical and radiological features with many spinal tumors. CASE REPORT: In this article, we present a 30-year-old lady who presented with low back pain and radicular neuropathic pain at L1 dermatome which was intractable to medical surgery. Her magnetic resonance imaging (MRI) of the lumbosacral spine revealed a T1 isointense, T2 heterogeneously hyperintense intradural extramedullary lesion at the conus medullaris with strong homogenous enhancement on contrast administration. The lesion was surgically excised completely with L1 laminectomy, and the histopathological picture was suggestive of paraganglioma. The patient's complaints resolved fully postoperatively, and there was no evidence of recurrence on long-term follow-up. CONCLUSION: Due to the absence of pathognomonic clinical or radiological features of paragangliomas, they should be taken into consideration in the differential diagnosis of spinal tumors. They share similar clinical and radiological features of schwannomas, ependymomas, and hemangioblastomas. The diagnosis is usually made postoperatively based on histopathological examination. Elsevier 2022-09-24 /pmc/articles/PMC9568865/ /pubmed/36167028 http://dx.doi.org/10.1016/j.ijscr.2022.107698 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Al-Salihi, Mohammed Maan Hussein, Muath Al-Jebur, Maryam Sabah Rahman, Sabrina Ayyad, Ali Rahman, Md Moshiur Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title | Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title_full | Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title_fullStr | Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title_full_unstemmed | Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title_short | Spinal paraganglioma at the conus medullaris mimicking schwannoma: A case report |
title_sort | spinal paraganglioma at the conus medullaris mimicking schwannoma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568865/ https://www.ncbi.nlm.nih.gov/pubmed/36167028 http://dx.doi.org/10.1016/j.ijscr.2022.107698 |
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