Articles producció científica> Medicina i Cirurgia

IgG4-Related Disease: Results From a Multicenter Spanish Registry

  • Dades identificatives

    Identificador: imarina:9351760
    Autors:
    Fernández-Codina, AMartínez-Valle, FPinilla, BLópez, CDeTorres, ISolans-Laqué, RFraile-Rodríguez, GCasanovas-Martínez, ALópez-Dupla, MRobles-Marhuenda, ABarragán-González, MJCid, MCPrieto-González, SBrito-Zerón, PCruces-Moreno, MTFonseca-Aizpuru, ELópez-Torres, MGil, JNúñez-Fernández, MJPardos-Gea, JSalvador-Cervelló, G
    Resum:
    IgG4-related disease (IgG4-RD) is a rare entity consisting of inflammation and fibrosis that has been described in multiple organs. Concrete diagnostic criteria have been established recently and there is a lack of large series of patients.To describe the clinical presentation, histopathological characteristics, treatment and evolution of a series of IgG4-RD Spanish patients.A retrospective multicenter study was performed. Twelve hospitals across Spain included patients meeting the current 2012 consensus criteria on IgG4-RD diagnosis.Fifty-five patients were included in the study, 38 of whom (69.1%) were male. Median age at diagnosis was 53 years. Thirty (54.5%) patients were included in the Histologically Highly Suggestive IgG4-RD group and 25 (45.5%) in the probable IgG4-RD group. Twenty-six (47.3%) patients had more than 1 organ affected at presentation. The most frequently affected organs were: retroperitoneum, orbital pseudotumor, pancreas, salivary and lachrymal glands, and maxillary sinuses.Corticosteroids were the mainstay of treatment (46 patients, 83.6%). Eighteen patients (32.7%) required additional immunosuppressive agents. Twenty-four (43.6%) patients achieved a complete response and 26 (43.7%) presented a partial response (<50% of regression) after 22 months of follow-up. No deaths were attributed directly to IgG4-RD and malignancy was infrequent.This is the largest IgG4-RD series reported in Europe. Patients were middle-aged males, with histologically probable IgG4-RD. The systemic form of the disease was frequent, involving mainly sites of the head and abdomen. Corticosteroids were an effective first line treatment, sometimes combined with immunosuppressive agents. Neither fatalities nor malignancies were attributed to IgG4-RD.
  • Altres:

    Autor segons l'article: Fernández-Codina, A; Martínez-Valle, F; Pinilla, B; López, C; DeTorres, I; Solans-Laqué, R; Fraile-Rodríguez, G; Casanovas-Martínez, A; López-Dupla, M; Robles-Marhuenda, A; Barragán-González, MJ; Cid, MC; Prieto-González, S; Brito-Zerón, P; Cruces-Moreno, MT; Fonseca-Aizpuru, E; López-Torres, M; Gil, J; Núñez-Fernández, MJ; Pardos-Gea, J; Salvador-Cervelló, G
    Departament: Medicina i Cirurgia
    Autor/s de la URV: López Dupla, Jesús Miguel
    Paraules clau: Systemic-disease Retroperitoneal fibrosis Prednisone Cohort Autoimmune pancreatitis
    Resum: IgG4-related disease (IgG4-RD) is a rare entity consisting of inflammation and fibrosis that has been described in multiple organs. Concrete diagnostic criteria have been established recently and there is a lack of large series of patients.To describe the clinical presentation, histopathological characteristics, treatment and evolution of a series of IgG4-RD Spanish patients.A retrospective multicenter study was performed. Twelve hospitals across Spain included patients meeting the current 2012 consensus criteria on IgG4-RD diagnosis.Fifty-five patients were included in the study, 38 of whom (69.1%) were male. Median age at diagnosis was 53 years. Thirty (54.5%) patients were included in the Histologically Highly Suggestive IgG4-RD group and 25 (45.5%) in the probable IgG4-RD group. Twenty-six (47.3%) patients had more than 1 organ affected at presentation. The most frequently affected organs were: retroperitoneum, orbital pseudotumor, pancreas, salivary and lachrymal glands, and maxillary sinuses.Corticosteroids were the mainstay of treatment (46 patients, 83.6%). Eighteen patients (32.7%) required additional immunosuppressive agents. Twenty-four (43.6%) patients achieved a complete response and 26 (43.7%) presented a partial response (<50% of regression) after 22 months of follow-up. No deaths were attributed directly to IgG4-RD and malignancy was infrequent.This is the largest IgG4-RD series reported in Europe. Patients were middle-aged males, with histologically probable IgG4-RD. The systemic form of the disease was frequent, involving mainly sites of the head and abdomen. Corticosteroids were an effective first line treatment, sometimes combined with immunosuppressive agents. Neither fatalities nor malignancies were attributed to IgG4-RD.
    Àrees temàtiques: Saúde coletiva Odontología Nutrição Medicine, general & internal Medicine (miscellaneous) Medicine (all) Medicina iii Medicina ii Medicina i Matemática / probabilidade e estatística Interdisciplinar Geografía General medicine Farmacia Ensino Engenharias iv Enfermagem Educação física Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Biotecnología Astronomia / física Antropologia / arqueologia
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: jesusmiguel.lopez@urv.cat
    Identificador de l'autor: 0000-0002-9141-2523
    Data d'alta del registre: 2024-09-07
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://journals.lww.com/md-journal/fulltext/2015/08020/igg4_related_disease__results_from_a_multicenter.21.aspx
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Medicine. 94 (32):
    Referència de l'ítem segons les normes APA: Fernández-Codina, A; Martínez-Valle, F; Pinilla, B; López, C; DeTorres, I; Solans-Laqué, R; Fraile-Rodríguez, G; Casanovas-Martínez, A; López-Dupla, M (2015). IgG4-Related Disease: Results From a Multicenter Spanish Registry. Medicine, 94(32), -. DOI: 10.1097/MD.0000000000001275
    DOI de l'article: 10.1097/MD.0000000000001275
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2015
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Medicine (Miscellaneous),Medicine, General & Internal
    Systemic-disease
    Retroperitoneal fibrosis
    Prednisone
    Cohort
    Autoimmune pancreatitis
    Saúde coletiva
    Odontología
    Nutrição
    Medicine, general & internal
    Medicine (miscellaneous)
    Medicine (all)
    Medicina iii
    Medicina ii
    Medicina i
    Matemática / probabilidade e estatística
    Interdisciplinar
    Geografía
    General medicine
    Farmacia
    Ensino
    Engenharias iv
    Enfermagem
    Educação física
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Biotecnología
    Astronomia / física
    Antropologia / arqueologia
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