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Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study

BACKGROUND: To determine the clinical presentation, current treatment and outcome of children with nonbacterial inflammatory bone disease. METHODS: Retrospective multicenter study of patients entered into the Swiss Pediatric Rheumatology Working Group registry with a diagnosis of chronic nonbacteria...

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Autores principales: Kaiser, Daniela, Bolt, Isabel, Hofer, Michael, Relly, Christa, Berthet, Gerald, Bolz, Dieter, Saurenmann, Traudel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473828/
https://www.ncbi.nlm.nih.gov/pubmed/26088861
http://dx.doi.org/10.1186/s12969-015-0023-y
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author Kaiser, Daniela
Bolt, Isabel
Hofer, Michael
Relly, Christa
Berthet, Gerald
Bolz, Dieter
Saurenmann, Traudel
author_facet Kaiser, Daniela
Bolt, Isabel
Hofer, Michael
Relly, Christa
Berthet, Gerald
Bolz, Dieter
Saurenmann, Traudel
author_sort Kaiser, Daniela
collection PubMed
description BACKGROUND: To determine the clinical presentation, current treatment and outcome of children with nonbacterial inflammatory bone disease. METHODS: Retrospective multicenter study of patients entered into the Swiss Pediatric Rheumatology Working Group registry with a diagnosis of chronic nonbacterial osteomyelitis (CNO) and synovitis acne pustulosis hyperostosis osteitis (SAPHO) syndrome. The charts were reviewed for informations about disease presentation, treatment, course and outcome. RESULTS: Forty-one children (31 girls and 10 boys) from 6 pediatric hospitals in Switzerland diagnosed between 1995 and 2010 were included in the study. The diagnosis was multifocal CNO (n = 33), unifocal CNO (n = 4) and SAPHO syndrome (n = 4). Mean age at onset of CNO was 9.5 years (range 1.4–15.6) and mean follow-up time was 52 months (range 6–156 months). Most patients (n = 27) had a chronic persistent disease course (>6 months), 8 patients had a course with one or more relapses and 6 patients had only one episode of CNO. Forty nine percent had received at least one course of antibiotics. In 57 % treatment with nonsteroidal anti-inflammatory drugs (NSAID) was sufficient to control the disease. Twelve out of 16 children with NSAID failure subsequently received corticosteroids, methotrexate, TNF α inhibitors, bisphosphonates or a combination of these drugs. CONCLUSIONS: In a multicenter cohort of 41 children 22 % started with unifocal lesion with a significant diagnostic delay. A higher proportion presented with chronic persistent disease than with a recurrent form. An osteomyelitis in the pelvic region is significantly associated with other features of juvenile spondylarthritis.
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spelling pubmed-44738282015-06-20 Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study Kaiser, Daniela Bolt, Isabel Hofer, Michael Relly, Christa Berthet, Gerald Bolz, Dieter Saurenmann, Traudel Pediatr Rheumatol Online J Research Article BACKGROUND: To determine the clinical presentation, current treatment and outcome of children with nonbacterial inflammatory bone disease. METHODS: Retrospective multicenter study of patients entered into the Swiss Pediatric Rheumatology Working Group registry with a diagnosis of chronic nonbacterial osteomyelitis (CNO) and synovitis acne pustulosis hyperostosis osteitis (SAPHO) syndrome. The charts were reviewed for informations about disease presentation, treatment, course and outcome. RESULTS: Forty-one children (31 girls and 10 boys) from 6 pediatric hospitals in Switzerland diagnosed between 1995 and 2010 were included in the study. The diagnosis was multifocal CNO (n = 33), unifocal CNO (n = 4) and SAPHO syndrome (n = 4). Mean age at onset of CNO was 9.5 years (range 1.4–15.6) and mean follow-up time was 52 months (range 6–156 months). Most patients (n = 27) had a chronic persistent disease course (>6 months), 8 patients had a course with one or more relapses and 6 patients had only one episode of CNO. Forty nine percent had received at least one course of antibiotics. In 57 % treatment with nonsteroidal anti-inflammatory drugs (NSAID) was sufficient to control the disease. Twelve out of 16 children with NSAID failure subsequently received corticosteroids, methotrexate, TNF α inhibitors, bisphosphonates or a combination of these drugs. CONCLUSIONS: In a multicenter cohort of 41 children 22 % started with unifocal lesion with a significant diagnostic delay. A higher proportion presented with chronic persistent disease than with a recurrent form. An osteomyelitis in the pelvic region is significantly associated with other features of juvenile spondylarthritis. BioMed Central 2015-06-19 /pmc/articles/PMC4473828/ /pubmed/26088861 http://dx.doi.org/10.1186/s12969-015-0023-y Text en © Kaiser et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kaiser, Daniela
Bolt, Isabel
Hofer, Michael
Relly, Christa
Berthet, Gerald
Bolz, Dieter
Saurenmann, Traudel
Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title_full Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title_fullStr Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title_full_unstemmed Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title_short Chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
title_sort chronic nonbacterial osteomyelitis in children: a retrospective multicenter study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473828/
https://www.ncbi.nlm.nih.gov/pubmed/26088861
http://dx.doi.org/10.1186/s12969-015-0023-y
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