ArticlePediatric rheumatology online journal2011
Long- term outcome of paediatric patients with ANCA vasculitis.
Article in Pediatric rheumatology online journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.
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Who cites it
21 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Childhood-onset granulomatosis with polyangiitis and microscopic polyangiitis: systematic review and meta-analysis.Orphanet journal of rare diseases · 2016Pooled it
- Microscopic polyangiitis in pediatric systemic lupus erythematosus: a unique presentation of pulmonary-renal syndrome and case report of an overlap syndrome.CEN case reports · 2025Article
- CAR T cell therapy for children with rheumatic disease: the time is now.Nature reviews. Rheumatology · 2025Review
- Pediatric ANCA vasculitis: clinical presentation, treatment, and outcomes in a French retrospective study.Pediatric nephrology (Berlin, Germany) · 2023Article
- Childhood-Onset ANCA- Associated Vasculitis: single center experience from Central California.Pediatric rheumatology online journal · 2023Article
- The Clinical and Pathological Features of Children With Microscopic Polyangiitis.Frontiers in pediatrics · 2021Article
- Article
- Biologics for childhood systemic vasculitis.Pediatric nephrology (Berlin, Germany) · 2019Review
- Epidemiology and Outcomes of Granulomatosis With Polyangiitis in Pediatric and Working-Age Adult Populations In the United States: Analysis of a Large National Claims Database.Arthritis & rheumatology (Hoboken, N.J.) · 2018Article
- Adolescent PR3-ANCA-positive hypertrophic pachymeningitis: A case report and review of the literature.Medicine · 2018Article
- Vasculitis update: pathogenesis and biomarkers.Pediatric nephrology (Berlin, Germany) · 2018Review
- Paediatric anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis: an update on renal management.Pediatric nephrology (Berlin, Germany) · 2018Review
- Pathogenesis and treatment of ANCA-associated vasculitis-a role for complement.Pediatric nephrology (Berlin, Germany) · 2018Review
- Outcome of kidney transplantation in pediatric patients with ANCA-associated glomerulonephritis: a single-center experience.Pediatric nephrology (Berlin, Germany) · 2017Article
- ANCA-associated vasculitis in childhood: recent advances.Italian journal of pediatrics · 2017Review
- Lung involvement in childhood onset granulomatosis with polyangiitis.Pediatric rheumatology online journal · 2017Review
- Clinical presentation and outcome of pediatric ANCA-associated glomerulonephritis.Pediatric nephrology (Berlin, Germany) · 2017Article
- Pauci-immune glomerulonephritis in children: a clinicopathologic study of 21 patients.Pediatric nephrology (Berlin, Germany) · 2015Article
- The new histopathologic classification of ANCA-associated GN and its association with renal outcomes in childhood.Clinical journal of the American Society of Nephrology : CJASN · 2014Article
- ANCA-associated glomerulonephritis/systemic vasculitis in childhood: clinical features-outcome.Pediatric nephrology (Berlin, Germany) · 2012Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPrimary systemic vasculitis presenting in childhood is an uncommon but serious condition. As these patients transfer to adult clinics for continuing care, defining long term outcomes with emphasis on disease and treatment- related morbidity and mortality is important. The aim of this study is to describe the long- term clinical course of paediatric patients with ANCA vasculitis.
methodsThe adult patients in our vasculitis clinics who had presented in childhood, with a follow up time of greater than 10 years were included. We also reviewed the literature for articles describing the clinical outcome of paediatric patients with ANCA vasculitis.
resultsWe describe the clinical course of 8 adults who presented in childhood with ANCA vasculitis. 7 patients had Wegener's granulomatosis and 1 had microscopic polyangiitis. The median age at presentation was 11.5 years, and follow up time ranged form 11 to 30 years. Induction therapy for all patients was steroids and/or cyclophosphamide. Maintenance therapy was with azathioprine or mycophenolate mofetil. Biological agents were used in 3 patients for relapsed disease in adulthood only.Seven patients achieved complete remission. All patients experienced disease relapse, with a median of 4 episodes. Kidney function was generally well preserved, with median eGFR 76 ml/min. Only one patient developed end-stage renal failure and one patient died after 25 years of disease. Treatment-related morbidity rates were high; 7 suffered from infections, 4 were infertile, 2 had skeletal complications, and 1 developed malignancy.
conclusionClose long- term follow up of paediatric patients with ANCA vasculitis is imperative, as this patient cohort is likely to live long enough to develop significant treatment and disease- related morbidities. Prospective cohort studies with novel therapies including paediatric patients are crucial to help us determine the best approach to managing this complex group of patients. In addition, although not yet observed in our series, late cardiovascular morbidity remains a major longer-term potential concern for adult survivors of paediatric vasculitis.
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