Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease

We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (...
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Autor*in:	Nobuhito Arakawa [verfasserIn] Hideaki Yamasawa [verfasserIn] Tamiko Takemura [verfasserIn] Shinya Okada [verfasserIn] Takafumi Taki [verfasserIn] Shigemi Ishikawa [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2020

Schlagwörter:	Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion

Übergeordnetes Werk:	In: Respirology Case Reports - Wiley, 2015, 8(2020), 2, Seite n/a-n/a
Übergeordnetes Werk:	volume:8 ; year:2020 ; number:2 ; pages:n/a-n/a

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1002/rcr2.512

Katalog-ID:	DOAJ034083634

Internformat


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520			\|a We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD.
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700	0		\|a Hideaki Yamasawa \|e verfasserin \|4 aut
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700	0		\|a Shigemi Ishikawa \|e verfasserin \|4 aut
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publishDate	2020
allfields	10.1002/rcr2.512 doi (DE-627)DOAJ034083634 (DE-599)DOAJ93054ea969994ce5b318ac3790a71897 DE-627 ger DE-627 rakwb eng RC705-779 Nobuhito Arakawa verfasserin aut Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD. Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system Hideaki Yamasawa verfasserin aut Tamiko Takemura verfasserin aut Shinya Okada verfasserin aut Takafumi Taki verfasserin aut Shigemi Ishikawa verfasserin aut In Respirology Case Reports Wiley, 2015 8(2020), 2, Seite n/a-n/a (DE-627)776632442 (DE-600)2750180-2 20513380 nnns volume:8 year:2020 number:2 pages:n/a-n/a https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/article/93054ea969994ce5b318ac3790a71897 kostenfrei https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/toc/2051-3380 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 8 2020 2 n/a-n/a
spelling	10.1002/rcr2.512 doi (DE-627)DOAJ034083634 (DE-599)DOAJ93054ea969994ce5b318ac3790a71897 DE-627 ger DE-627 rakwb eng RC705-779 Nobuhito Arakawa verfasserin aut Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD. Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system Hideaki Yamasawa verfasserin aut Tamiko Takemura verfasserin aut Shinya Okada verfasserin aut Takafumi Taki verfasserin aut Shigemi Ishikawa verfasserin aut In Respirology Case Reports Wiley, 2015 8(2020), 2, Seite n/a-n/a (DE-627)776632442 (DE-600)2750180-2 20513380 nnns volume:8 year:2020 number:2 pages:n/a-n/a https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/article/93054ea969994ce5b318ac3790a71897 kostenfrei https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/toc/2051-3380 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 8 2020 2 n/a-n/a
allfields_unstemmed	10.1002/rcr2.512 doi (DE-627)DOAJ034083634 (DE-599)DOAJ93054ea969994ce5b318ac3790a71897 DE-627 ger DE-627 rakwb eng RC705-779 Nobuhito Arakawa verfasserin aut Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD. Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system Hideaki Yamasawa verfasserin aut Tamiko Takemura verfasserin aut Shinya Okada verfasserin aut Takafumi Taki verfasserin aut Shigemi Ishikawa verfasserin aut In Respirology Case Reports Wiley, 2015 8(2020), 2, Seite n/a-n/a (DE-627)776632442 (DE-600)2750180-2 20513380 nnns volume:8 year:2020 number:2 pages:n/a-n/a https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/article/93054ea969994ce5b318ac3790a71897 kostenfrei https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/toc/2051-3380 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 8 2020 2 n/a-n/a
allfieldsGer	10.1002/rcr2.512 doi (DE-627)DOAJ034083634 (DE-599)DOAJ93054ea969994ce5b318ac3790a71897 DE-627 ger DE-627 rakwb eng RC705-779 Nobuhito Arakawa verfasserin aut Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD. Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system Hideaki Yamasawa verfasserin aut Tamiko Takemura verfasserin aut Shinya Okada verfasserin aut Takafumi Taki verfasserin aut Shigemi Ishikawa verfasserin aut In Respirology Case Reports Wiley, 2015 8(2020), 2, Seite n/a-n/a (DE-627)776632442 (DE-600)2750180-2 20513380 nnns volume:8 year:2020 number:2 pages:n/a-n/a https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/article/93054ea969994ce5b318ac3790a71897 kostenfrei https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/toc/2051-3380 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 8 2020 2 n/a-n/a
allfieldsSound	10.1002/rcr2.512 doi (DE-627)DOAJ034083634 (DE-599)DOAJ93054ea969994ce5b318ac3790a71897 DE-627 ger DE-627 rakwb eng RC705-779 Nobuhito Arakawa verfasserin aut Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD. Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system Hideaki Yamasawa verfasserin aut Tamiko Takemura verfasserin aut Shinya Okada verfasserin aut Takafumi Taki verfasserin aut Shigemi Ishikawa verfasserin aut In Respirology Case Reports Wiley, 2015 8(2020), 2, Seite n/a-n/a (DE-627)776632442 (DE-600)2750180-2 20513380 nnns volume:8 year:2020 number:2 pages:n/a-n/a https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/article/93054ea969994ce5b318ac3790a71897 kostenfrei https://doi.org/10.1002/rcr2.512 kostenfrei https://doaj.org/toc/2051-3380 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 8 2020 2 n/a-n/a
language	English
source	In Respirology Case Reports 8(2020), 2, Seite n/a-n/a volume:8 year:2020 number:2 pages:n/a-n/a
sourceStr	In Respirology Case Reports 8(2020), 2, Seite n/a-n/a volume:8 year:2020 number:2 pages:n/a-n/a
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion Diseases of the respiratory system
isfreeaccess_bool	true
container_title	Respirology Case Reports
authorswithroles_txt_mv	Nobuhito Arakawa @@aut@@ Hideaki Yamasawa @@aut@@ Tamiko Takemura @@aut@@ Shinya Okada @@aut@@ Takafumi Taki @@aut@@ Shigemi Ishikawa @@aut@@
publishDateDaySort_date	2020-01-01T00:00:00Z
hierarchy_top_id	776632442
id	DOAJ034083634
language_de	englisch
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callnumber-first	R - Medicine
author	Nobuhito Arakawa
spellingShingle	Nobuhito Arakawa misc RC705-779 misc Hyperplasia of lymphoid follicles misc IgG4‐related lung disease misc interstitial pneumonia with autoimmune features misc multidisciplinary discussion misc pulmonary venous occlusion misc Diseases of the respiratory system Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease
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topic_title	RC705-779 Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease Hyperplasia of lymphoid follicles IgG4‐related lung disease interstitial pneumonia with autoimmune features multidisciplinary discussion pulmonary venous occlusion
topic	misc RC705-779 misc Hyperplasia of lymphoid follicles misc IgG4‐related lung disease misc interstitial pneumonia with autoimmune features misc multidisciplinary discussion misc pulmonary venous occlusion misc Diseases of the respiratory system
topic_unstemmed	misc RC705-779 misc Hyperplasia of lymphoid follicles misc IgG4‐related lung disease misc interstitial pneumonia with autoimmune features misc multidisciplinary discussion misc pulmonary venous occlusion misc Diseases of the respiratory system
topic_browse	misc RC705-779 misc Hyperplasia of lymphoid follicles misc IgG4‐related lung disease misc interstitial pneumonia with autoimmune features misc multidisciplinary discussion misc pulmonary venous occlusion misc Diseases of the respiratory system
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title	Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease
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title_full	Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease
author_sort	Nobuhito Arakawa
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author_browse	Nobuhito Arakawa Hideaki Yamasawa Tamiko Takemura Shinya Okada Takafumi Taki Shigemi Ishikawa
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title_sort	interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for igg4‐related respiratory disease
callnumber	RC705-779
title_auth	Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease
abstract	We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD.
abstractGer	We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD.
abstract_unstemmed	We held a multidisciplinary discussion (MDD) about a 61‐year‐old woman who had an interstitial lung disease (ILD) without extrathoracic lesions that met the classification criteria for interstitial pneumonia with autoimmune features (IPAF) and the proposed diagnostic criteria for immunoglobulin G4 (IgG4)‐related respiratory disease (IgG4‐RRD). Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. We concluded that the present case was IPAF that met the proposed diagnostic criteria for IgG4‐RRD.
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container_issue	2
title_short	Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease
url	https://doi.org/10.1002/rcr2.512 https://doaj.org/article/93054ea969994ce5b318ac3790a71897 https://doaj.org/toc/2051-3380
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up_date	2024-07-03T21:19:15.187Z
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Clinically, the marked progression of lung‐limited diffuse lesions was consistent with IPAF. Serum IgG4 and rheumatoid factor levels simultaneously increased and did not contribute to a diagnosis. Pathologically, the significant hyperplasia of lymphoid follicles was consistent with rheumatoid arthritis (RA)‐associated ILD. Pulmonary venous occlusions by intimal fibrosis and intimal thickening were not important because these occlusions are found in IgG4‐related lung disease (IgG4‐RLD) and also in IPAF or ILDs related to connective tissue diseases (CTDs). Radiologically, fibrosing shadows that remained in the lung periphery after treatment were compatible with RA‐associated chronic ILD. 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Interstitial pneumonia with autoimmune features that met the proposed diagnostic criteria for IgG4‐related respiratory disease

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