Immunoglobulin G4-related disease preceded by lung involvement: A case report
Immunoglobulin G4-related disease (IgG4-RD) is a systemic condition involving various organs and vessels including the pancreas, bile duct, salivary glands, periorbital tissues, kidneys, lungs, lymph nodes, meninges, and aorta. Recently, some cases of IgG4-RD have been reported, in which only pulmon...
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Veröffentlicht in: | Medicine (Baltimore) 2017-06, Vol.96 (24), p.e7086-e7086 |
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creator | Abo, Miki Takato, Hazuki Watanabe, Satoshi Kase, Kazumasa Sakai, Tamami Koba, Hayato Hara, Johsuke Sone, Takashi Kimura, Hideharu Kasahara, Kazuo |
description | Immunoglobulin G4-related disease (IgG4-RD) is a systemic condition involving various organs and vessels including the pancreas, bile duct, salivary glands, periorbital tissues, kidneys, lungs, lymph nodes, meninges, and aorta. Recently, some cases of IgG4-RD have been reported, in which only pulmonary lesions were present. It is not known whether IgG4-RD can be diagnosed on the basis of pulmonary lesions only, because increases in serum IgG4 levels and infiltration of IgG4-positive plasma cells into the lung tissue also occur in other inflammatory conditions. A case of IgG-RD that was followed-up for 7 years after onset is described.
Initially, only pulmonary lesions were present; however, other lesions in the submandibular glands, pancreas, periarterial region, and other areas occurred over time, with a gradual increase in serum IgG4 levels.
Histopathology results from the patient's submandibular gland confirmed the diagnosis of IgG4-RD. Following diagnosis, the patient was treated with corticosteroids immediately, and his symptoms disappeared rapidly.
Because other diseases, including malignancies, mimic IgG4-RD in clinical and histopathological features, an absolute diagnosis is necessary to avoid missing the presence of underlying diseases. This case more provides insight into the clinical pathology of IgG4-RD. |
doi_str_mv | 10.1097/MD.0000000000007086 |
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Initially, only pulmonary lesions were present; however, other lesions in the submandibular glands, pancreas, periarterial region, and other areas occurred over time, with a gradual increase in serum IgG4 levels.
Histopathology results from the patient's submandibular gland confirmed the diagnosis of IgG4-RD. Following diagnosis, the patient was treated with corticosteroids immediately, and his symptoms disappeared rapidly.
Because other diseases, including malignancies, mimic IgG4-RD in clinical and histopathological features, an absolute diagnosis is necessary to avoid missing the presence of underlying diseases. This case more provides insight into the clinical pathology of IgG4-RD.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000007086</identifier><identifier>PMID: 28614225</identifier><language>eng</language><publisher>United States: The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Aged ; Autoimmune Diseases - blood ; Autoimmune Diseases - diagnosis ; Autoimmune Diseases - drug therapy ; Autoimmune Diseases - pathology ; Clinical Case Report ; Diagnosis, Differential ; Humans ; Immunoglobulin G - blood ; Lung - diagnostic imaging ; Lung - drug effects ; Lung - pathology ; Lung Diseases - diagnosis ; Lung Diseases - drug therapy ; Lung Diseases - immunology ; Lung Diseases - pathology ; Male</subject><ispartof>Medicine (Baltimore), 2017-06, Vol.96 (24), p.e7086-e7086</ispartof><rights>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3551-2f01119563b1cb5cdc22e2dd157a5b5f7cbce33b42f22f797f6f66a4e2ce81f73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478310/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478310/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28614225$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abo, Miki</creatorcontrib><creatorcontrib>Takato, Hazuki</creatorcontrib><creatorcontrib>Watanabe, Satoshi</creatorcontrib><creatorcontrib>Kase, Kazumasa</creatorcontrib><creatorcontrib>Sakai, Tamami</creatorcontrib><creatorcontrib>Koba, Hayato</creatorcontrib><creatorcontrib>Hara, Johsuke</creatorcontrib><creatorcontrib>Sone, Takashi</creatorcontrib><creatorcontrib>Kimura, Hideharu</creatorcontrib><creatorcontrib>Kasahara, Kazuo</creatorcontrib><title>Immunoglobulin G4-related disease preceded by lung involvement: A case report</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Immunoglobulin G4-related disease (IgG4-RD) is a systemic condition involving various organs and vessels including the pancreas, bile duct, salivary glands, periorbital tissues, kidneys, lungs, lymph nodes, meninges, and aorta. Recently, some cases of IgG4-RD have been reported, in which only pulmonary lesions were present. It is not known whether IgG4-RD can be diagnosed on the basis of pulmonary lesions only, because increases in serum IgG4 levels and infiltration of IgG4-positive plasma cells into the lung tissue also occur in other inflammatory conditions. A case of IgG-RD that was followed-up for 7 years after onset is described.
Initially, only pulmonary lesions were present; however, other lesions in the submandibular glands, pancreas, periarterial region, and other areas occurred over time, with a gradual increase in serum IgG4 levels.
Histopathology results from the patient's submandibular gland confirmed the diagnosis of IgG4-RD. Following diagnosis, the patient was treated with corticosteroids immediately, and his symptoms disappeared rapidly.
Because other diseases, including malignancies, mimic IgG4-RD in clinical and histopathological features, an absolute diagnosis is necessary to avoid missing the presence of underlying diseases. This case more provides insight into the clinical pathology of IgG4-RD.</description><subject>Aged</subject><subject>Autoimmune Diseases - blood</subject><subject>Autoimmune Diseases - diagnosis</subject><subject>Autoimmune Diseases - drug therapy</subject><subject>Autoimmune Diseases - pathology</subject><subject>Clinical Case Report</subject><subject>Diagnosis, Differential</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Lung - diagnostic imaging</subject><subject>Lung - drug effects</subject><subject>Lung - pathology</subject><subject>Lung Diseases - diagnosis</subject><subject>Lung Diseases - drug therapy</subject><subject>Lung Diseases - immunology</subject><subject>Lung Diseases - pathology</subject><subject>Male</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1P3DAQhi3UCra0vwAJ5dhLqMefGw6V0EIpEqte4Gw5zng34MRbO1nEv2-2C4h2LiPNPPPOFyEnQM-AVvrb8vKMvjNN5-qAzEByVcpKiQ9kRimTpa60OCKfcn6gFLhm4pAcsbkCwZickeVN1419XIVYj6Hti2tRJgx2wKZo2ow2Y7FJ6LCZAvVzEcZ-VbT9NoYtdtgP58VF4XZQwk1Mw2fy0duQ8cuLPyb3P67uFj_L21_XN4uL29JxKaFkngJAJRWvwdXSNY4xZE0DUltZS69d7ZDzWjDPmJ8W8MorZQUyh3Pwmh-T73vdzVh32LhpkmSD2aS2s-nZRNuafzN9uzaruDVS6DkHOgl8fRFI8feIeTBdmx2GYHuMYzZQTRBXXOx68T3qUsw5oX9rA9TsHmGWl-b_R0xVp-8nfKt5vfwEiD3wFMOAKT-G8QmTWaMNw_qvntQVKxkFTRUoWk4RAP4HwJaUEA</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Abo, Miki</creator><creator>Takato, Hazuki</creator><creator>Watanabe, Satoshi</creator><creator>Kase, Kazumasa</creator><creator>Sakai, Tamami</creator><creator>Koba, Hayato</creator><creator>Hara, Johsuke</creator><creator>Sone, Takashi</creator><creator>Kimura, Hideharu</creator><creator>Kasahara, Kazuo</creator><general>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170601</creationdate><title>Immunoglobulin G4-related disease preceded by lung involvement: A case report</title><author>Abo, Miki ; Takato, Hazuki ; Watanabe, Satoshi ; Kase, Kazumasa ; Sakai, Tamami ; Koba, Hayato ; Hara, Johsuke ; Sone, Takashi ; Kimura, Hideharu ; Kasahara, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3551-2f01119563b1cb5cdc22e2dd157a5b5f7cbce33b42f22f797f6f66a4e2ce81f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Autoimmune Diseases - blood</topic><topic>Autoimmune Diseases - diagnosis</topic><topic>Autoimmune Diseases - drug therapy</topic><topic>Autoimmune Diseases - pathology</topic><topic>Clinical Case Report</topic><topic>Diagnosis, Differential</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Lung - diagnostic imaging</topic><topic>Lung - drug effects</topic><topic>Lung - pathology</topic><topic>Lung Diseases - diagnosis</topic><topic>Lung Diseases - drug therapy</topic><topic>Lung Diseases - immunology</topic><topic>Lung Diseases - pathology</topic><topic>Male</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abo, Miki</creatorcontrib><creatorcontrib>Takato, Hazuki</creatorcontrib><creatorcontrib>Watanabe, Satoshi</creatorcontrib><creatorcontrib>Kase, Kazumasa</creatorcontrib><creatorcontrib>Sakai, Tamami</creatorcontrib><creatorcontrib>Koba, Hayato</creatorcontrib><creatorcontrib>Hara, Johsuke</creatorcontrib><creatorcontrib>Sone, Takashi</creatorcontrib><creatorcontrib>Kimura, Hideharu</creatorcontrib><creatorcontrib>Kasahara, Kazuo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abo, Miki</au><au>Takato, Hazuki</au><au>Watanabe, Satoshi</au><au>Kase, Kazumasa</au><au>Sakai, Tamami</au><au>Koba, Hayato</au><au>Hara, Johsuke</au><au>Sone, Takashi</au><au>Kimura, Hideharu</au><au>Kasahara, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunoglobulin G4-related disease preceded by lung involvement: A case report</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>96</volume><issue>24</issue><spage>e7086</spage><epage>e7086</epage><pages>e7086-e7086</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Immunoglobulin G4-related disease (IgG4-RD) is a systemic condition involving various organs and vessels including the pancreas, bile duct, salivary glands, periorbital tissues, kidneys, lungs, lymph nodes, meninges, and aorta. Recently, some cases of IgG4-RD have been reported, in which only pulmonary lesions were present. It is not known whether IgG4-RD can be diagnosed on the basis of pulmonary lesions only, because increases in serum IgG4 levels and infiltration of IgG4-positive plasma cells into the lung tissue also occur in other inflammatory conditions. A case of IgG-RD that was followed-up for 7 years after onset is described.
Initially, only pulmonary lesions were present; however, other lesions in the submandibular glands, pancreas, periarterial region, and other areas occurred over time, with a gradual increase in serum IgG4 levels.
Histopathology results from the patient's submandibular gland confirmed the diagnosis of IgG4-RD. Following diagnosis, the patient was treated with corticosteroids immediately, and his symptoms disappeared rapidly.
Because other diseases, including malignancies, mimic IgG4-RD in clinical and histopathological features, an absolute diagnosis is necessary to avoid missing the presence of underlying diseases. This case more provides insight into the clinical pathology of IgG4-RD.</abstract><cop>United States</cop><pub>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>28614225</pmid><doi>10.1097/MD.0000000000007086</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aged Autoimmune Diseases - blood Autoimmune Diseases - diagnosis Autoimmune Diseases - drug therapy Autoimmune Diseases - pathology Clinical Case Report Diagnosis, Differential Humans Immunoglobulin G - blood Lung - diagnostic imaging Lung - drug effects Lung - pathology Lung Diseases - diagnosis Lung Diseases - drug therapy Lung Diseases - immunology Lung Diseases - pathology Male |
title | Immunoglobulin G4-related disease preceded by lung involvement: A case report |
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