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IgG4-related disease: a systematic review of this unrecognized disease in pediatrics
BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibro-inflammatory condition with an unclear pathophysiological mechanism affecting different parts of the body. If untreated, the disease can lead to fibrosis and irreversible organ damage. IgG4-RD mostly has been described in ad...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807566/ https://www.ncbi.nlm.nih.gov/pubmed/27012661 http://dx.doi.org/10.1186/s12969-016-0079-3 |
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author | Karim, Faiz Loeffen, Jan Bramer, Wichor Westenberg, Lauren Verdijk, Rob van Hagen, Martin van Laar, Jan |
author_facet | Karim, Faiz Loeffen, Jan Bramer, Wichor Westenberg, Lauren Verdijk, Rob van Hagen, Martin van Laar, Jan |
author_sort | Karim, Faiz |
collection | PubMed |
description | BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibro-inflammatory condition with an unclear pathophysiological mechanism affecting different parts of the body. If untreated, the disease can lead to fibrosis and irreversible organ damage. IgG4-RD mostly has been described in adults, hence it is generally unknown among pediatricians. This systematic search of the literature provides an overview of all reports published on IgG4-RD in children in order to create awareness of IgG4-RD in pediatrics and to emphasize the broad clinical presentation of this disease. METHODS: A systematic literature search of Embase, Medline, Web-of-Science, PubMed publisher, Cochrane and Google Scholar was performed for case reports on IgG4-RD in children. RESULTS: Of total 740 articles identified by the search, 22 case reports including 25 cases of IgG4-RD in children were found. The median age of the children was 13 years, of which 64 % were girls. IgG4-related orbital disease (44 %) and autoimmune pancreatitis type 1/IgG4-related pancreatitis (12 %) predominantly occurred. Less frequently, other manifestations as pulmonary manifestation, cholangitis and lymphadenopathy were also found. Almost all cases were histologically proven. Prednisone was the first choice of treatment leading to favorable clinical response in 83 % of the cases. Maintenance therapy with steroid sparing agents was required in 43 % of the cases needing therapy. Rituximab was successful in all 4 cases, whereas, the disease modifying rheumatic drugs (DMARDs) mycophenolate mofetil, azathioprine and methotrexate were effective in almost 50 % of the cases. CONCLUSION: IgG4-RD in children is a generally unknown disease among pediatricians, but several pediatric cases have been described. Prednisone is the first choice of treatment leading to disease remission in the majority of the cases. DMARDs and rituximab are alternative effective steroid sparing agents with more positive evidence for the latter. |
format | Online Article Text |
id | pubmed-4807566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48075662016-03-25 IgG4-related disease: a systematic review of this unrecognized disease in pediatrics Karim, Faiz Loeffen, Jan Bramer, Wichor Westenberg, Lauren Verdijk, Rob van Hagen, Martin van Laar, Jan Pediatr Rheumatol Online J Review BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is a systemic fibro-inflammatory condition with an unclear pathophysiological mechanism affecting different parts of the body. If untreated, the disease can lead to fibrosis and irreversible organ damage. IgG4-RD mostly has been described in adults, hence it is generally unknown among pediatricians. This systematic search of the literature provides an overview of all reports published on IgG4-RD in children in order to create awareness of IgG4-RD in pediatrics and to emphasize the broad clinical presentation of this disease. METHODS: A systematic literature search of Embase, Medline, Web-of-Science, PubMed publisher, Cochrane and Google Scholar was performed for case reports on IgG4-RD in children. RESULTS: Of total 740 articles identified by the search, 22 case reports including 25 cases of IgG4-RD in children were found. The median age of the children was 13 years, of which 64 % were girls. IgG4-related orbital disease (44 %) and autoimmune pancreatitis type 1/IgG4-related pancreatitis (12 %) predominantly occurred. Less frequently, other manifestations as pulmonary manifestation, cholangitis and lymphadenopathy were also found. Almost all cases were histologically proven. Prednisone was the first choice of treatment leading to favorable clinical response in 83 % of the cases. Maintenance therapy with steroid sparing agents was required in 43 % of the cases needing therapy. Rituximab was successful in all 4 cases, whereas, the disease modifying rheumatic drugs (DMARDs) mycophenolate mofetil, azathioprine and methotrexate were effective in almost 50 % of the cases. CONCLUSION: IgG4-RD in children is a generally unknown disease among pediatricians, but several pediatric cases have been described. Prednisone is the first choice of treatment leading to disease remission in the majority of the cases. DMARDs and rituximab are alternative effective steroid sparing agents with more positive evidence for the latter. BioMed Central 2016-03-25 /pmc/articles/PMC4807566/ /pubmed/27012661 http://dx.doi.org/10.1186/s12969-016-0079-3 Text en © Karim et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Karim, Faiz Loeffen, Jan Bramer, Wichor Westenberg, Lauren Verdijk, Rob van Hagen, Martin van Laar, Jan IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title | IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title_full | IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title_fullStr | IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title_full_unstemmed | IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title_short | IgG4-related disease: a systematic review of this unrecognized disease in pediatrics |
title_sort | igg4-related disease: a systematic review of this unrecognized disease in pediatrics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807566/ https://www.ncbi.nlm.nih.gov/pubmed/27012661 http://dx.doi.org/10.1186/s12969-016-0079-3 |
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