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IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature

Immunoglobulin G4-related disease (IgG4-RD) is known for forming soft tissue mass lesions that may have compressive effects. It is an extremely rare disease that most frequently affects the pancreas causing autoimmune pancreatitis. It can also affect the gallbladder, salivary glands, and lacrimal gl...

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Autores principales: Merza, Nooraldin, Taha, Ahmed, Lung, John, Benderman, Anthony W., Wright, Stephen E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604497/
https://www.ncbi.nlm.nih.gov/pubmed/31316844
http://dx.doi.org/10.1155/2019/3618510
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author Merza, Nooraldin
Taha, Ahmed
Lung, John
Benderman, Anthony W.
Wright, Stephen E.
author_facet Merza, Nooraldin
Taha, Ahmed
Lung, John
Benderman, Anthony W.
Wright, Stephen E.
author_sort Merza, Nooraldin
collection PubMed
description Immunoglobulin G4-related disease (IgG4-RD) is known for forming soft tissue mass lesions that may have compressive effects. It is an extremely rare disease that most frequently affects the pancreas causing autoimmune pancreatitis. It can also affect the gallbladder, salivary glands, and lacrimal glands causing respective organ-specific complications. In our report, we describe an IgG4-RD case that affected the spinal cord. A 60-year-old female presented with cervical spinal cord compression caused by IgG4-RD leading to several neurological deficits. Pathological examination of the excisional biopsy of the mass revealed dense lymphoplasmacytic cells infiltration and stromal fibrosis with IgG4 and plasma cells. The patient showed a dramatic response to the administration of systemic steroids with almost resolution of her neurological symptoms. This case highlights the first case in literature for IgG4-RD of the extradural tissue causing spinal compression. Hereby, we also demonstrate the dramatic response of IgG4-RD to the administration of systemic steroids as the patient had no recurrence after 5 years of close follow-up, the longest reported period of follow-up reported in the literature to date.
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spelling pubmed-66044972019-07-17 IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature Merza, Nooraldin Taha, Ahmed Lung, John Benderman, Anthony W. Wright, Stephen E. Case Reports Immunol Case Report Immunoglobulin G4-related disease (IgG4-RD) is known for forming soft tissue mass lesions that may have compressive effects. It is an extremely rare disease that most frequently affects the pancreas causing autoimmune pancreatitis. It can also affect the gallbladder, salivary glands, and lacrimal glands causing respective organ-specific complications. In our report, we describe an IgG4-RD case that affected the spinal cord. A 60-year-old female presented with cervical spinal cord compression caused by IgG4-RD leading to several neurological deficits. Pathological examination of the excisional biopsy of the mass revealed dense lymphoplasmacytic cells infiltration and stromal fibrosis with IgG4 and plasma cells. The patient showed a dramatic response to the administration of systemic steroids with almost resolution of her neurological symptoms. This case highlights the first case in literature for IgG4-RD of the extradural tissue causing spinal compression. Hereby, we also demonstrate the dramatic response of IgG4-RD to the administration of systemic steroids as the patient had no recurrence after 5 years of close follow-up, the longest reported period of follow-up reported in the literature to date. Hindawi 2019-06-18 /pmc/articles/PMC6604497/ /pubmed/31316844 http://dx.doi.org/10.1155/2019/3618510 Text en Copyright © 2019 Nooraldin Merza et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Merza, Nooraldin
Taha, Ahmed
Lung, John
Benderman, Anthony W.
Wright, Stephen E.
IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title_full IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title_fullStr IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title_full_unstemmed IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title_short IgG4-Related Sclerosing Disease Causing Spinal Cord Compression: The First Reported Case in Literature
title_sort igg4-related sclerosing disease causing spinal cord compression: the first reported case in literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604497/
https://www.ncbi.nlm.nih.gov/pubmed/31316844
http://dx.doi.org/10.1155/2019/3618510
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