IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review
Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary a...
Ausführliche Beschreibung
Autor*in: |
Okamoto, Shota [verfasserIn] Tsuboi, Hiroto [verfasserIn] Sato, Ryota [verfasserIn] Terasaki, Mayu [verfasserIn] Terasaki, Toshihiko [verfasserIn] Toko, Hirofumi [verfasserIn] Shimizu, Masaru [verfasserIn] Honda, Fumika [verfasserIn] Yagishita, Mizuki [verfasserIn] Ohyama, Ayako [verfasserIn] Kurata, Izumi [verfasserIn] Abe, Saori [verfasserIn] Takahashi, Hiroyuki [verfasserIn] Osada, Atsumu [verfasserIn] Hagiwara, Shinya [verfasserIn] Kondo, Yuya [verfasserIn] Matsumoto, Isao [verfasserIn] Sumida, Takayuki [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Rheumatology international - Berlin : Springer, 1981, 40(2020), 10 vom: 23. März, Seite 1725-1732 |
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Übergeordnetes Werk: |
volume:40 ; year:2020 ; number:10 ; day:23 ; month:03 ; pages:1725-1732 |
Links: |
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DOI / URN: |
10.1007/s00296-020-04555-y |
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Katalog-ID: |
SPR040784622 |
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520 | |a Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. | ||
650 | 4 | |a IgG4-related disease |7 (dpeaa)DE-He213 | |
650 | 4 | |a Pleural disease |7 (dpeaa)DE-He213 | |
650 | 4 | |a Periaortitis |7 (dpeaa)DE-He213 | |
650 | 4 | |a Submandibular gland |7 (dpeaa)DE-He213 | |
700 | 1 | |a Tsuboi, Hiroto |e verfasserin |4 aut | |
700 | 1 | |a Sato, Ryota |e verfasserin |4 aut | |
700 | 1 | |a Terasaki, Mayu |e verfasserin |4 aut | |
700 | 1 | |a Terasaki, Toshihiko |e verfasserin |4 aut | |
700 | 1 | |a Toko, Hirofumi |e verfasserin |4 aut | |
700 | 1 | |a Shimizu, Masaru |e verfasserin |4 aut | |
700 | 1 | |a Honda, Fumika |e verfasserin |4 aut | |
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700 | 1 | |a Takahashi, Hiroyuki |e verfasserin |4 aut | |
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700 | 1 | |a Hagiwara, Shinya |e verfasserin |4 aut | |
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700 | 1 | |a Matsumoto, Isao |e verfasserin |4 aut | |
700 | 1 | |a Sumida, Takayuki |e verfasserin |4 aut | |
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10.1007/s00296-020-04555-y doi (DE-627)SPR040784622 (SPR)s00296-020-04555-y-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.83 bkl Okamoto, Shota verfasserin aut IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 Tsuboi, Hiroto verfasserin aut Sato, Ryota verfasserin aut Terasaki, Mayu verfasserin aut Terasaki, Toshihiko verfasserin aut Toko, Hirofumi verfasserin aut Shimizu, Masaru verfasserin aut Honda, Fumika verfasserin aut Yagishita, Mizuki verfasserin aut Ohyama, Ayako verfasserin aut Kurata, Izumi verfasserin aut Abe, Saori verfasserin aut Takahashi, Hiroyuki verfasserin aut Osada, Atsumu verfasserin aut Hagiwara, Shinya verfasserin aut Kondo, Yuya verfasserin aut Matsumoto, Isao verfasserin aut Sumida, Takayuki verfasserin aut Enthalten in Rheumatology international Berlin : Springer, 1981 40(2020), 10 vom: 23. März, Seite 1725-1732 (DE-627)265508320 (DE-600)1464208-6 1437-160X nnns volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 https://dx.doi.org/10.1007/s00296-020-04555-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.83 ASE AR 40 2020 10 23 03 1725-1732 |
spelling |
10.1007/s00296-020-04555-y doi (DE-627)SPR040784622 (SPR)s00296-020-04555-y-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.83 bkl Okamoto, Shota verfasserin aut IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 Tsuboi, Hiroto verfasserin aut Sato, Ryota verfasserin aut Terasaki, Mayu verfasserin aut Terasaki, Toshihiko verfasserin aut Toko, Hirofumi verfasserin aut Shimizu, Masaru verfasserin aut Honda, Fumika verfasserin aut Yagishita, Mizuki verfasserin aut Ohyama, Ayako verfasserin aut Kurata, Izumi verfasserin aut Abe, Saori verfasserin aut Takahashi, Hiroyuki verfasserin aut Osada, Atsumu verfasserin aut Hagiwara, Shinya verfasserin aut Kondo, Yuya verfasserin aut Matsumoto, Isao verfasserin aut Sumida, Takayuki verfasserin aut Enthalten in Rheumatology international Berlin : Springer, 1981 40(2020), 10 vom: 23. März, Seite 1725-1732 (DE-627)265508320 (DE-600)1464208-6 1437-160X nnns volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 https://dx.doi.org/10.1007/s00296-020-04555-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.83 ASE AR 40 2020 10 23 03 1725-1732 |
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10.1007/s00296-020-04555-y doi (DE-627)SPR040784622 (SPR)s00296-020-04555-y-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.83 bkl Okamoto, Shota verfasserin aut IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 Tsuboi, Hiroto verfasserin aut Sato, Ryota verfasserin aut Terasaki, Mayu verfasserin aut Terasaki, Toshihiko verfasserin aut Toko, Hirofumi verfasserin aut Shimizu, Masaru verfasserin aut Honda, Fumika verfasserin aut Yagishita, Mizuki verfasserin aut Ohyama, Ayako verfasserin aut Kurata, Izumi verfasserin aut Abe, Saori verfasserin aut Takahashi, Hiroyuki verfasserin aut Osada, Atsumu verfasserin aut Hagiwara, Shinya verfasserin aut Kondo, Yuya verfasserin aut Matsumoto, Isao verfasserin aut Sumida, Takayuki verfasserin aut Enthalten in Rheumatology international Berlin : Springer, 1981 40(2020), 10 vom: 23. März, Seite 1725-1732 (DE-627)265508320 (DE-600)1464208-6 1437-160X nnns volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 https://dx.doi.org/10.1007/s00296-020-04555-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.83 ASE AR 40 2020 10 23 03 1725-1732 |
allfieldsGer |
10.1007/s00296-020-04555-y doi (DE-627)SPR040784622 (SPR)s00296-020-04555-y-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.83 bkl Okamoto, Shota verfasserin aut IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 Tsuboi, Hiroto verfasserin aut Sato, Ryota verfasserin aut Terasaki, Mayu verfasserin aut Terasaki, Toshihiko verfasserin aut Toko, Hirofumi verfasserin aut Shimizu, Masaru verfasserin aut Honda, Fumika verfasserin aut Yagishita, Mizuki verfasserin aut Ohyama, Ayako verfasserin aut Kurata, Izumi verfasserin aut Abe, Saori verfasserin aut Takahashi, Hiroyuki verfasserin aut Osada, Atsumu verfasserin aut Hagiwara, Shinya verfasserin aut Kondo, Yuya verfasserin aut Matsumoto, Isao verfasserin aut Sumida, Takayuki verfasserin aut Enthalten in Rheumatology international Berlin : Springer, 1981 40(2020), 10 vom: 23. März, Seite 1725-1732 (DE-627)265508320 (DE-600)1464208-6 1437-160X nnns volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 https://dx.doi.org/10.1007/s00296-020-04555-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.83 ASE AR 40 2020 10 23 03 1725-1732 |
allfieldsSound |
10.1007/s00296-020-04555-y doi (DE-627)SPR040784622 (SPR)s00296-020-04555-y-e DE-627 ger DE-627 rakwb eng 610 ASE 610 ASE 44.83 bkl Okamoto, Shota verfasserin aut IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 Tsuboi, Hiroto verfasserin aut Sato, Ryota verfasserin aut Terasaki, Mayu verfasserin aut Terasaki, Toshihiko verfasserin aut Toko, Hirofumi verfasserin aut Shimizu, Masaru verfasserin aut Honda, Fumika verfasserin aut Yagishita, Mizuki verfasserin aut Ohyama, Ayako verfasserin aut Kurata, Izumi verfasserin aut Abe, Saori verfasserin aut Takahashi, Hiroyuki verfasserin aut Osada, Atsumu verfasserin aut Hagiwara, Shinya verfasserin aut Kondo, Yuya verfasserin aut Matsumoto, Isao verfasserin aut Sumida, Takayuki verfasserin aut Enthalten in Rheumatology international Berlin : Springer, 1981 40(2020), 10 vom: 23. März, Seite 1725-1732 (DE-627)265508320 (DE-600)1464208-6 1437-160X nnns volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 https://dx.doi.org/10.1007/s00296-020-04555-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.83 ASE AR 40 2020 10 23 03 1725-1732 |
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Enthalten in Rheumatology international 40(2020), 10 vom: 23. März, Seite 1725-1732 volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 |
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Enthalten in Rheumatology international 40(2020), 10 vom: 23. März, Seite 1725-1732 volume:40 year:2020 number:10 day:23 month:03 pages:1725-1732 |
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IgG4-related disease Pleural disease Periaortitis Submandibular gland |
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Rheumatology international |
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Okamoto, Shota @@aut@@ Tsuboi, Hiroto @@aut@@ Sato, Ryota @@aut@@ Terasaki, Mayu @@aut@@ Terasaki, Toshihiko @@aut@@ Toko, Hirofumi @@aut@@ Shimizu, Masaru @@aut@@ Honda, Fumika @@aut@@ Yagishita, Mizuki @@aut@@ Ohyama, Ayako @@aut@@ Kurata, Izumi @@aut@@ Abe, Saori @@aut@@ Takahashi, Hiroyuki @@aut@@ Osada, Atsumu @@aut@@ Hagiwara, Shinya @@aut@@ Kondo, Yuya @@aut@@ Matsumoto, Isao @@aut@@ Sumida, Takayuki @@aut@@ |
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2020-03-23T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR040784622</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519092408.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201007s2020 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s00296-020-04555-y</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR040784622</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s00296-020-04555-y-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">44.83</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Okamoto, Shota</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2020</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. 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|
author |
Okamoto, Shota |
spellingShingle |
Okamoto, Shota ddc 610 bkl 44.83 misc IgG4-related disease misc Pleural disease misc Periaortitis misc Submandibular gland IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
authorStr |
Okamoto, Shota |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)265508320 |
format |
electronic Article |
dewey-ones |
610 - Medicine & health |
delete_txt_mv |
keep |
author_role |
aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut aut |
collection |
springer |
remote_str |
true |
illustrated |
Not Illustrated |
issn |
1437-160X |
topic_title |
610 ASE 44.83 bkl IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review IgG4-related disease (dpeaa)DE-He213 Pleural disease (dpeaa)DE-He213 Periaortitis (dpeaa)DE-He213 Submandibular gland (dpeaa)DE-He213 |
topic |
ddc 610 bkl 44.83 misc IgG4-related disease misc Pleural disease misc Periaortitis misc Submandibular gland |
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IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
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IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
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Okamoto, Shota Tsuboi, Hiroto Sato, Ryota Terasaki, Mayu Terasaki, Toshihiko Toko, Hirofumi Shimizu, Masaru Honda, Fumika Yagishita, Mizuki Ohyama, Ayako Kurata, Izumi Abe, Saori Takahashi, Hiroyuki Osada, Atsumu Hagiwara, Shinya Kondo, Yuya Matsumoto, Isao Sumida, Takayuki |
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igg4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
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IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
abstract |
Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. |
abstractGer |
Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. |
abstract_unstemmed |
Abstract IgG4-related disease (IgG4-RD) is a fibro-inflammatory condition characterized by increased serum IgG4 level, infiltration of lymphocytes and IgG4-positive ($ IgG4^{+} $) plasma cells and fibrosis. It can occur in almost all organs, commonly affecting the pancreas, biliary tract, salivary and lacrimal glands and kidneys. However, reports of IgG4-RD accompanied by pathologically confirmed, IgG4-related pleural disease are scarce. Here, we present a case of a 64-year-old man with suspected malignant pleural mesothelioma based on imaging findings but finally diagnosed with IgG4-RD (including pleuritis, periaortitis and bilateral submandibular gland enlargement) based on a high serum IgG4 level and pleural histopathological findings such as lymphoplasmacytic infiltration including $ IgG4^{+} $ plasma cells and fibrosis. Systemic corticosteroid therapy was effective at reducing serum IgG4, improving bilateral submandibular gland enlargement, and regressing pleural thickening and periaortic soft tissue. We also discuss clinical characteristics and pleural pathological features of previously reported cases with IgG4-related pleural disease based on a comprehensive literature review. Our case of IgG4-RD with pleura, aorta and submandibular gland involvement, pathologically confirmed by pleural specimen might be unique and very rare. |
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IgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based review |
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score |
7.4001513 |