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Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis

Some forms of idiopathic retroperitoneal fibrosis (RF) have recently been considered to be a part of the spectrum of immunoglobulin G4 (IgG4)-related disease. This case report is the first description of a spontaneous remission in a patient with pathologically proven IgG4-related RF. Although the pa...

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Autores principales: Yamakawa, Hideaki, Sekine, Akimasa, Yamanaka, Yumie, Sadoyama, Shinko, Baba, Tomohisa, Hagiwara, Eri, Okudela, Koji, Ogura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548681/
https://www.ncbi.nlm.nih.gov/pubmed/28717084
http://dx.doi.org/10.2169/internalmedicine.56.7996
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author Yamakawa, Hideaki
Sekine, Akimasa
Yamanaka, Yumie
Sadoyama, Shinko
Baba, Tomohisa
Hagiwara, Eri
Okudela, Koji
Ogura, Takashi
author_facet Yamakawa, Hideaki
Sekine, Akimasa
Yamanaka, Yumie
Sadoyama, Shinko
Baba, Tomohisa
Hagiwara, Eri
Okudela, Koji
Ogura, Takashi
author_sort Yamakawa, Hideaki
collection PubMed
description Some forms of idiopathic retroperitoneal fibrosis (RF) have recently been considered to be a part of the spectrum of immunoglobulin G4 (IgG4)-related disease. This case report is the first description of a spontaneous remission in a patient with pathologically proven IgG4-related RF. Although the pathogenesis and long-term disease behavior of IgG4-related RF remains unknown, we believe that an initial assessment consisting of only careful monitoring might be one important strategy, especially in asymptomatic IgG4-related RF patients without nephropathy, while carefully monitoring these patients for the risk of recurrence.
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spelling pubmed-55486812017-08-11 Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis Yamakawa, Hideaki Sekine, Akimasa Yamanaka, Yumie Sadoyama, Shinko Baba, Tomohisa Hagiwara, Eri Okudela, Koji Ogura, Takashi Intern Med Case Report Some forms of idiopathic retroperitoneal fibrosis (RF) have recently been considered to be a part of the spectrum of immunoglobulin G4 (IgG4)-related disease. This case report is the first description of a spontaneous remission in a patient with pathologically proven IgG4-related RF. Although the pathogenesis and long-term disease behavior of IgG4-related RF remains unknown, we believe that an initial assessment consisting of only careful monitoring might be one important strategy, especially in asymptomatic IgG4-related RF patients without nephropathy, while carefully monitoring these patients for the risk of recurrence. The Japanese Society of Internal Medicine 2017-07-15 /pmc/articles/PMC5548681/ /pubmed/28717084 http://dx.doi.org/10.2169/internalmedicine.56.7996 Text en Copyright © 2017 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yamakawa, Hideaki
Sekine, Akimasa
Yamanaka, Yumie
Sadoyama, Shinko
Baba, Tomohisa
Hagiwara, Eri
Okudela, Koji
Ogura, Takashi
Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title_full Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title_fullStr Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title_full_unstemmed Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title_short Pathologically Proven Spontaneous Remission of IgG4-related Retroperitoneal Fibrosis
title_sort pathologically proven spontaneous remission of igg4-related retroperitoneal fibrosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548681/
https://www.ncbi.nlm.nih.gov/pubmed/28717084
http://dx.doi.org/10.2169/internalmedicine.56.7996
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