Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)

Detalhes bibliográficos
Autor(a) principal: Bohm, Marek
Data de Publicação: 2014
Outros Autores: Fernandez, Maria Isabel Gonzalez, Ozen, Seza, Pistorio, Angela, Dolezalova, Pavla, Brogan, Paul, Barbano, Giancarlo, Sengler, Claudia, Klein-Gitelman, Marisa, Quartier, Pierre, Fasth, Anders, Herlin, Troels, Terreri, Maria Teresa R. A. [UNIFESP], Nielsen, Susan, van Rossum, Marion A. J., Avcin, Tadej, Rodolfo Castell, Esteban, Foeldvari, Ivan, Foell, Dirk, Kondi, Anuela, Kone-Paut, Isabelle, Kuester, Rolf-Michael, Michels, Hartmut, Wulffraat, Nico, Ben Amer, Halima, Malattia, Clara, Martini, Alberto, Ruperto, Nicolino, Paediat Rheumatology Int
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1186/1546-0096-12-18
http://repositorio.unifesp.br/handle/11600/37782
Resumo: Background: Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis (WG), belongs to the group of ANCA-associated necrotizing vasculitides. This study describes the clinical picture of the disease in a large cohort of GPA paediatric patients.Children with age at diagnosis <= 18 years, fulfilling the EULAR/PRINTO/PRES GPA/WG classification criteria were extracted from the PRINTO vasculitis database. the clinical signs/symptoms and laboratory features were analysed before or at the time of diagnosis and at least 3 months thereafter and compared with other paediatric and adult case series (>50 patients) derived from the literature.Findings: the 56 children with GPA/WG were predominantly females (68%) and Caucasians (82%) with a median age at disease onset of 11.7 years, and a median delay in diagnosis of 4.2 months. the most frequent organ systems involved before/at the time of diagnosis were ears, nose, throat (91%), constitutional (malaise, fever, weight loss) (89%), respiratory (79%), mucosa and skin (64%), musculoskeletal (59%), and eye (35%), 67% were ANCA-PR3 positive, while haematuria/proteinuria was present in > 50% of the children. in adult series, the frequency of female involvement ranged from 29% to 50% with lower frequencies of constitutional (fever, weight loss), ears, nose, throat (oral/nasal ulceration, otitis/aural discharge), respiratory (tracheal/endobronchial stenosis/obstruction), laboratory involvement and higher frequency of conductive hearing loss than in this paediatric series.Conclusions: Paediatric patients compared to adults with GPA/WG have similar pattern of clinical manifestations but different frequencies of organ involvement.
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spelling Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)Wegener's granulomatosisGranulomatosis with polyangiitisClinical studyClinical picture of diseaseComparison with literatureBackground: Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis (WG), belongs to the group of ANCA-associated necrotizing vasculitides. This study describes the clinical picture of the disease in a large cohort of GPA paediatric patients.Children with age at diagnosis <= 18 years, fulfilling the EULAR/PRINTO/PRES GPA/WG classification criteria were extracted from the PRINTO vasculitis database. the clinical signs/symptoms and laboratory features were analysed before or at the time of diagnosis and at least 3 months thereafter and compared with other paediatric and adult case series (>50 patients) derived from the literature.Findings: the 56 children with GPA/WG were predominantly females (68%) and Caucasians (82%) with a median age at disease onset of 11.7 years, and a median delay in diagnosis of 4.2 months. the most frequent organ systems involved before/at the time of diagnosis were ears, nose, throat (91%), constitutional (malaise, fever, weight loss) (89%), respiratory (79%), mucosa and skin (64%), musculoskeletal (59%), and eye (35%), 67% were ANCA-PR3 positive, while haematuria/proteinuria was present in > 50% of the children. in adult series, the frequency of female involvement ranged from 29% to 50% with lower frequencies of constitutional (fever, weight loss), ears, nose, throat (oral/nasal ulceration, otitis/aural discharge), respiratory (tracheal/endobronchial stenosis/obstruction), laboratory involvement and higher frequency of conductive hearing loss than in this paediatric series.Conclusions: Paediatric patients compared to adults with GPA/WG have similar pattern of clinical manifestations but different frequencies of organ involvement.PRINTO, Ist Giannina Gaslini Pediat Reumatol 2, Genoa, ItalyCharles Univ Prague, Fac Med 1, Prague, Czech RepublicGen Univ Hosp Prague, Prague, Czech RepublicHacettepe Univ, Childrens Hosp, Dept Pediat Rheumatol & Nephrol, Ankara, TurkeyIst Giannina Gaslini, Serv Epidemiol & Biostat, I-16148 Genoa, ItalyNHS Fdn Trust, Great Ormond St Hosp, Dept Rheumatol, London, EnglandIst Giannina Gaslini, I-16148 Genoa, ItalyCharite, Dept Pediat, Div Pneumol & Immunol, D-13353 Berlin, GermanyAnn & Robert H Lurie Childrens Hosp Chicago, Chicago, IL USAUniv Paris 05, Unit Immunol Hematol & Rhumatol Pediat, Ctr Reference Natl Arthrit Juveniles, Hop Necker Enfants Malad,Inst IMAGINE, Paris, FranceUniv Gothenburg, Dept Pediat, Queen Silvia Childrens Hosp, Gothenburg, SwedenAarhus Univ Hosp, Skejby Sygehus, Dept Pediat, Pediat Rheumatol Clin, DK-8000 Aarhus, DenmarkUniversidade Federal de São Paulo, São Paulo, BrazilRigshosp, Juliane Marie Centret, Pediat Klin 2, DK-2100 Copenhagen, DenmarkEmma Children Hosp AMC, Dept Pediat, Amsterdam, NetherlandsUniv Childrens Hosp, Univ Med Ctr Ljubljana, Dept Allergol Rheumatol & Clin Immunol, Ljubljana, SloveniaHosp Dr Felipe Glasman, Rheumatolgy Sect, Buenos Aires, DF, ArgentinaKlinikum Eilbek Hs 6, Hamburger Zentrum Kinder & Jugendrheumatol, Hamburg, GermanyUniv Childrens Hosp, Dept Pediat Rheumatol & Immunol, Munster, GermanyUniv Hosp Ctr, Dept Pediat, Tirana, AlbaniaUniv Paris 11, APHP, CHU Le Kremlin Bicetre, CEREMAI Ctr Reference Natl Malad Autoinflammat Rh, Paris, FranceAsklepios Klin Altona, Hamburg, GermanyKinderklin Garmisch Partenkirchen gGmbH, Deutsch Zentrum Kinder & Jugendrheumatol, Garmisch Partenkirchen, GermanyWilhelmina Childrens Hosp, Dept Pediat Immunol & Rheumatol, Utrecht, NetherlandsBenghazi Children Hosp Benghazi, MUB Rheumatol Clin, Benghazi, LibyaUniv Genoa, Dipartimento Pediat, Genoa, ItalyPediatrics, Universidade Federal de São Paulo, São Paulo, BrazilWeb of ScienceIstituto G. GasliniPaediatric Rheumatology International Trials Organisation (PRINTO), Genoa, ItalyCharles University Grant AgencyEuropean League Against Rheumatism (EULAR) Scientific Training BursariesCharles University Grant Agency: GAUK 52608/2008Biomed Central LtdPRINTOCharles Univ PragueGen Univ Hosp PragueHacettepe UnivIst Giannina GasliniNHS Fdn TrustChariteAnn & Robert H Lurie Childrens Hosp ChicagoUniv Paris 05Univ GothenburgAarhus Univ HospUniversidade Federal de São Paulo (UNIFESP)RigshospEmma Children Hosp AMCUniv Childrens HospHosp Dr Felipe GlasmanKlinikum Eilbek Hs 6Univ Hosp CtrUniv Paris 11Asklepios Klin AltonaKinderklin Garmisch Partenkirchen gGmbHWilhelmina Childrens HospBenghazi Children Hosp BenghaziUniv GenoaBohm, MarekFernandez, Maria Isabel GonzalezOzen, SezaPistorio, AngelaDolezalova, PavlaBrogan, PaulBarbano, GiancarloSengler, ClaudiaKlein-Gitelman, MarisaQuartier, PierreFasth, AndersHerlin, TroelsTerreri, Maria Teresa R. A. [UNIFESP]Nielsen, Susanvan Rossum, Marion A. J.Avcin, TadejRodolfo Castell, EstebanFoeldvari, IvanFoell, DirkKondi, AnuelaKone-Paut, IsabelleKuester, Rolf-MichaelMichels, HartmutWulffraat, NicoBen Amer, HalimaMalattia, ClaraMartini, AlbertoRuperto, NicolinoPaediat Rheumatology Int2016-01-24T14:37:18Z2016-01-24T14:37:18Z2014-05-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion5application/pdfhttp://dx.doi.org/10.1186/1546-0096-12-18Pediatric Rheumatology. London: Biomed Central Ltd, v. 12, 5 p., 2014.10.1186/1546-0096-12-18WOS000336749400001.pdf1546-0096http://repositorio.unifesp.br/handle/11600/37782WOS:000336749400001engPediatric Rheumatologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T09:39:03Zoai:repositorio.unifesp.br/:11600/37782Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T09:39:03Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
title Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
spellingShingle Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
Bohm, Marek
Wegener's granulomatosis
Granulomatosis with polyangiitis
Clinical study
Clinical picture of disease
Comparison with literature
title_short Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
title_full Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
title_fullStr Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
title_full_unstemmed Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
title_sort Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
author Bohm, Marek
author_facet Bohm, Marek
Fernandez, Maria Isabel Gonzalez
Ozen, Seza
Pistorio, Angela
Dolezalova, Pavla
Brogan, Paul
Barbano, Giancarlo
Sengler, Claudia
Klein-Gitelman, Marisa
Quartier, Pierre
Fasth, Anders
Herlin, Troels
Terreri, Maria Teresa R. A. [UNIFESP]
Nielsen, Susan
van Rossum, Marion A. J.
Avcin, Tadej
Rodolfo Castell, Esteban
Foeldvari, Ivan
Foell, Dirk
Kondi, Anuela
Kone-Paut, Isabelle
Kuester, Rolf-Michael
Michels, Hartmut
Wulffraat, Nico
Ben Amer, Halima
Malattia, Clara
Martini, Alberto
Ruperto, Nicolino
Paediat Rheumatology Int
author_role author
author2 Fernandez, Maria Isabel Gonzalez
Ozen, Seza
Pistorio, Angela
Dolezalova, Pavla
Brogan, Paul
Barbano, Giancarlo
Sengler, Claudia
Klein-Gitelman, Marisa
Quartier, Pierre
Fasth, Anders
Herlin, Troels
Terreri, Maria Teresa R. A. [UNIFESP]
Nielsen, Susan
van Rossum, Marion A. J.
Avcin, Tadej
Rodolfo Castell, Esteban
Foeldvari, Ivan
Foell, Dirk
Kondi, Anuela
Kone-Paut, Isabelle
Kuester, Rolf-Michael
Michels, Hartmut
Wulffraat, Nico
Ben Amer, Halima
Malattia, Clara
Martini, Alberto
Ruperto, Nicolino
Paediat Rheumatology Int
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv PRINTO
Charles Univ Prague
Gen Univ Hosp Prague
Hacettepe Univ
Ist Giannina Gaslini
NHS Fdn Trust
Charite
Ann & Robert H Lurie Childrens Hosp Chicago
Univ Paris 05
Univ Gothenburg
Aarhus Univ Hosp
Universidade Federal de São Paulo (UNIFESP)
Rigshosp
Emma Children Hosp AMC
Univ Childrens Hosp
Hosp Dr Felipe Glasman
Klinikum Eilbek Hs 6
Univ Hosp Ctr
Univ Paris 11
Asklepios Klin Altona
Kinderklin Garmisch Partenkirchen gGmbH
Wilhelmina Childrens Hosp
Benghazi Children Hosp Benghazi
Univ Genoa
dc.contributor.author.fl_str_mv Bohm, Marek
Fernandez, Maria Isabel Gonzalez
Ozen, Seza
Pistorio, Angela
Dolezalova, Pavla
Brogan, Paul
Barbano, Giancarlo
Sengler, Claudia
Klein-Gitelman, Marisa
Quartier, Pierre
Fasth, Anders
Herlin, Troels
Terreri, Maria Teresa R. A. [UNIFESP]
Nielsen, Susan
van Rossum, Marion A. J.
Avcin, Tadej
Rodolfo Castell, Esteban
Foeldvari, Ivan
Foell, Dirk
Kondi, Anuela
Kone-Paut, Isabelle
Kuester, Rolf-Michael
Michels, Hartmut
Wulffraat, Nico
Ben Amer, Halima
Malattia, Clara
Martini, Alberto
Ruperto, Nicolino
Paediat Rheumatology Int
dc.subject.por.fl_str_mv Wegener's granulomatosis
Granulomatosis with polyangiitis
Clinical study
Clinical picture of disease
Comparison with literature
topic Wegener's granulomatosis
Granulomatosis with polyangiitis
Clinical study
Clinical picture of disease
Comparison with literature
description Background: Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis (WG), belongs to the group of ANCA-associated necrotizing vasculitides. This study describes the clinical picture of the disease in a large cohort of GPA paediatric patients.Children with age at diagnosis <= 18 years, fulfilling the EULAR/PRINTO/PRES GPA/WG classification criteria were extracted from the PRINTO vasculitis database. the clinical signs/symptoms and laboratory features were analysed before or at the time of diagnosis and at least 3 months thereafter and compared with other paediatric and adult case series (>50 patients) derived from the literature.Findings: the 56 children with GPA/WG were predominantly females (68%) and Caucasians (82%) with a median age at disease onset of 11.7 years, and a median delay in diagnosis of 4.2 months. the most frequent organ systems involved before/at the time of diagnosis were ears, nose, throat (91%), constitutional (malaise, fever, weight loss) (89%), respiratory (79%), mucosa and skin (64%), musculoskeletal (59%), and eye (35%), 67% were ANCA-PR3 positive, while haematuria/proteinuria was present in > 50% of the children. in adult series, the frequency of female involvement ranged from 29% to 50% with lower frequencies of constitutional (fever, weight loss), ears, nose, throat (oral/nasal ulceration, otitis/aural discharge), respiratory (tracheal/endobronchial stenosis/obstruction), laboratory involvement and higher frequency of conductive hearing loss than in this paediatric series.Conclusions: Paediatric patients compared to adults with GPA/WG have similar pattern of clinical manifestations but different frequencies of organ involvement.
publishDate 2014
dc.date.none.fl_str_mv 2014-05-26
2016-01-24T14:37:18Z
2016-01-24T14:37:18Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1546-0096-12-18
Pediatric Rheumatology. London: Biomed Central Ltd, v. 12, 5 p., 2014.
10.1186/1546-0096-12-18
WOS000336749400001.pdf
1546-0096
http://repositorio.unifesp.br/handle/11600/37782
WOS:000336749400001
url http://dx.doi.org/10.1186/1546-0096-12-18
http://repositorio.unifesp.br/handle/11600/37782
identifier_str_mv Pediatric Rheumatology. London: Biomed Central Ltd, v. 12, 5 p., 2014.
10.1186/1546-0096-12-18
WOS000336749400001.pdf
1546-0096
WOS:000336749400001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pediatric Rheumatology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 5
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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