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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...

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Autores principales: Gader, Ghassen, Atig, Fatma Ben, Jemel, Nesrine, Bourgou, Malek, Slimane, Abdelhafidh, Ghedira, Khalil, Badri, Mohamed, Zammel, Ihsèn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
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.
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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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