ANCA-associated vasculitis in childhood

Marta Calatroni, Elena Oliva, Davide Gianfreda, Gina Gregorini, Marco Allinovi, Giuseppe A Ramirez, Enrica P Bozzolo, Sara Monti, Claudia Bracaglia, Giulia Marucci, Monica Bodria, Renato A Sinico, Federico Pieruzzi, Gabriella Moroni, Serena Pastore, Giacomo Emmi, Mariagrazia Catanoso, Giancarlo Barbano, Alice Bonanni, Augusto Vaglio

Research output: Contribution to journalArticle

Abstract

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides are rare systemic diseases that usually occur in adulthood. They comprise granulomatosis with polyangiitis (GPA, Wegener's), microscopic polyangiitis (MPA) and eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss syndrome). Their clinical presentation is often heterogeneous, with frequent involvement of the respiratory tract, the kidney, the skin and the joints. ANCA-associated vasculitis is rare in childhood but North-American and European cohort studies performed during the last decade have clarified their phenotype, patterns of renal involvement and their prognostic implications, and outcome. Herein, we review the main clinical and therapeutic aspects of childhood-onset ANCA-associated vasculitis, and provide preliminary data on demographic characteristics and organ manifestations of an Italian multicentre cohort.
Original languageEnglish
JournalItalian Journal of Pediatrics
Volume43
Issue number1
DOIs
Publication statusPublished - May 5 2017

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Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
Granulomatosis with Polyangiitis
Microscopic Polyangiitis
Churg-Strauss Syndrome
Kidney
Rare Diseases
Respiratory System
Cohort Studies
Joints
Demography
Phenotype
Skin
Therapeutics

Keywords

  • Journal Article
  • Review

Cite this

Calatroni, M., Oliva, E., Gianfreda, D., Gregorini, G., Allinovi, M., Ramirez, G. A., ... Vaglio, A. (2017). ANCA-associated vasculitis in childhood. Italian Journal of Pediatrics, 43(1). https://doi.org/10.1186/s13052-017-0364-x

ANCA-associated vasculitis in childhood. / Calatroni, Marta; Oliva, Elena; Gianfreda, Davide; Gregorini, Gina; Allinovi, Marco; Ramirez, Giuseppe A; Bozzolo, Enrica P; Monti, Sara; Bracaglia, Claudia; Marucci, Giulia; Bodria, Monica; Sinico, Renato A; Pieruzzi, Federico; Moroni, Gabriella; Pastore, Serena; Emmi, Giacomo; Catanoso, Mariagrazia; Barbano, Giancarlo; Bonanni, Alice; Vaglio, Augusto.

In: Italian Journal of Pediatrics, Vol. 43, No. 1, 05.05.2017.

Research output: Contribution to journalArticle

Calatroni, M, Oliva, E, Gianfreda, D, Gregorini, G, Allinovi, M, Ramirez, GA, Bozzolo, EP, Monti, S, Bracaglia, C, Marucci, G, Bodria, M, Sinico, RA, Pieruzzi, F, Moroni, G, Pastore, S, Emmi, G, Catanoso, M, Barbano, G, Bonanni, A & Vaglio, A 2017, 'ANCA-associated vasculitis in childhood', Italian Journal of Pediatrics, vol. 43, no. 1. https://doi.org/10.1186/s13052-017-0364-x
Calatroni M, Oliva E, Gianfreda D, Gregorini G, Allinovi M, Ramirez GA et al. ANCA-associated vasculitis in childhood. Italian Journal of Pediatrics. 2017 May 5;43(1). https://doi.org/10.1186/s13052-017-0364-x
Calatroni, Marta ; Oliva, Elena ; Gianfreda, Davide ; Gregorini, Gina ; Allinovi, Marco ; Ramirez, Giuseppe A ; Bozzolo, Enrica P ; Monti, Sara ; Bracaglia, Claudia ; Marucci, Giulia ; Bodria, Monica ; Sinico, Renato A ; Pieruzzi, Federico ; Moroni, Gabriella ; Pastore, Serena ; Emmi, Giacomo ; Catanoso, Mariagrazia ; Barbano, Giancarlo ; Bonanni, Alice ; Vaglio, Augusto. / ANCA-associated vasculitis in childhood. In: Italian Journal of Pediatrics. 2017 ; Vol. 43, No. 1.
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AU - Calatroni, Marta

AU - Oliva, Elena

AU - Gianfreda, Davide

AU - Gregorini, Gina

AU - Allinovi, Marco

AU - Ramirez, Giuseppe A

AU - Bozzolo, Enrica P

AU - Monti, Sara

AU - Bracaglia, Claudia

AU - Marucci, Giulia

AU - Bodria, Monica

AU - Sinico, Renato A

AU - Pieruzzi, Federico

AU - Moroni, Gabriella

AU - Pastore, Serena

AU - Emmi, Giacomo

AU - Catanoso, Mariagrazia

AU - Barbano, Giancarlo

AU - Bonanni, Alice

AU - Vaglio, Augusto

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AB - Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides are rare systemic diseases that usually occur in adulthood. They comprise granulomatosis with polyangiitis (GPA, Wegener's), microscopic polyangiitis (MPA) and eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss syndrome). Their clinical presentation is often heterogeneous, with frequent involvement of the respiratory tract, the kidney, the skin and the joints. ANCA-associated vasculitis is rare in childhood but North-American and European cohort studies performed during the last decade have clarified their phenotype, patterns of renal involvement and their prognostic implications, and outcome. Herein, we review the main clinical and therapeutic aspects of childhood-onset ANCA-associated vasculitis, and provide preliminary data on demographic characteristics and organ manifestations of an Italian multicentre cohort.

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KW - Review

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M3 - Article

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JO - Italian Journal of Pediatrics

JF - Italian Journal of Pediatrics

SN - 1720-8424

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