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Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression
BACKGROUND: Inflammatory pseudotumors are rare, and those attributed to immunoglobulin G4 (IgG4) diseases are even less frequently encountered. Here, we reviewed 41 cases from the literature of spinal inflammatory pseudotumors due to IgG4 and have added our single new case. CASE PRESENTATION: A 25-y...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316182/ https://www.ncbi.nlm.nih.gov/pubmed/37404483 http://dx.doi.org/10.25259/SNI_400_2023 |
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author | Gader, Ghassen Atig, Fatma Ben Jemel, Nesrine Bourgou, Malek Slimane, Abdelhafidh Ghedira, Khalil Badri, Mohamed Zammel, Ihsèn |
author_facet | Gader, Ghassen Atig, Fatma Ben Jemel, Nesrine Bourgou, Malek Slimane, Abdelhafidh Ghedira, Khalil Badri, Mohamed Zammel, Ihsèn |
author_sort | Gader, Ghassen |
collection | PubMed |
description | BACKGROUND: Inflammatory pseudotumors are rare, and those attributed to immunoglobulin G4 (IgG4) diseases are even less frequently encountered. Here, we reviewed 41 cases from the literature of spinal inflammatory pseudotumors due to IgG4 and have added our single new case. CASE PRESENTATION: A 25-year-old male presented with progressive back pain, bilateral paraparesis, and sphincter dysfunction. His deficit was attributed to MR-documented posterolateral lesion between the T5 and T10 levels for which he levels underwent a T1–T1010 laminectomy. The pathology revealed an immunoglobulin G4-related inflammatory pseudotumor. Postoperatively, the patient additionally required systemic and epidural administration of glucocorticoids. CONCLUSION: IgG4-related disease is an emerging clinical condition that rarely involves the central nervous system. Spinal inflammatory pseudotumors, including IgG4 disease, should be more commonly considered among the potential differential diagnoses of lesions compressing the spinal cord. |
format | Online Article Text |
id | pubmed-10316182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-103161822023-07-04 Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression Gader, Ghassen Atig, Fatma Ben Jemel, Nesrine Bourgou, Malek Slimane, Abdelhafidh Ghedira, Khalil Badri, Mohamed Zammel, Ihsèn Surg Neurol Int Case Report BACKGROUND: Inflammatory pseudotumors are rare, and those attributed to immunoglobulin G4 (IgG4) diseases are even less frequently encountered. Here, we reviewed 41 cases from the literature of spinal inflammatory pseudotumors due to IgG4 and have added our single new case. CASE PRESENTATION: A 25-year-old male presented with progressive back pain, bilateral paraparesis, and sphincter dysfunction. His deficit was attributed to MR-documented posterolateral lesion between the T5 and T10 levels for which he levels underwent a T1–T1010 laminectomy. The pathology revealed an immunoglobulin G4-related inflammatory pseudotumor. Postoperatively, the patient additionally required systemic and epidural administration of glucocorticoids. CONCLUSION: IgG4-related disease is an emerging clinical condition that rarely involves the central nervous system. Spinal inflammatory pseudotumors, including IgG4 disease, should be more commonly considered among the potential differential diagnoses of lesions compressing the spinal cord. Scientific Scholar 2023-06-16 /pmc/articles/PMC10316182/ /pubmed/37404483 http://dx.doi.org/10.25259/SNI_400_2023 Text en Copyright: © 2023 Surgical Neurology International https://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, transform, 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 Gader, Ghassen Atig, Fatma Ben Jemel, Nesrine Bourgou, Malek Slimane, Abdelhafidh Ghedira, Khalil Badri, Mohamed Zammel, Ihsèn Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title | Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title_full | Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title_fullStr | Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title_full_unstemmed | Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title_short | Epiduritis related to IgG4 disease: A very rare cause for spinal cord compression |
title_sort | epiduritis related to igg4 disease: a very rare cause for spinal cord compression |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316182/ https://www.ncbi.nlm.nih.gov/pubmed/37404483 http://dx.doi.org/10.25259/SNI_400_2023 |
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