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. 2016 Aug 30;14(1):47.
doi: 10.1186/s12969-016-0109-1.

Chronic recurrent multifocal osteomyelitis (CRMO) - advancing the diagnosis

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Chronic recurrent multifocal osteomyelitis (CRMO) - advancing the diagnosis

M R Roderick et al. Pediatr Rheumatol Online J. .

Abstract

Background: Chronic recurrent multifocal osteomyelitis (CRMO) is a little known inflammatory bone disease occurring primarily in children and adolescents. Delays in referral and diagnosis may lead to prolonged courses of antibiotics with in-patient care, unnecessary radiation exposure from multiple plain radiographs or bone scans and repeated surgery including bone biopsies. Children (aged < 18 years) diagnosed with CRMO between January 2005 and December 2012, reviewed at Bristol Royal Hospital for Children were included and all available data collected. Information regarding CRMO was sent to all orthopaedic surgeons in the region in 2009. The aim of the study was to examine the features of the cohort, to examine the length of time to diagnosis and to explore the criteria used for diagnosis with and without biopsy.

Findings: Over an 8 year period, 41 patients were diagnosed with CRMO. Symptom onset occurred at a median of 9 years of age and time to diagnosis had a median of 15 months (range 0-92). Correlation coefficient analysis for time to diagnosis by year showed statistical significance with a decreasing trend. From the cohort data, diagnostic criteria were developed; applied retrospectively, 34 (83 %) children may have been diagnosed using the criteria, without a biopsy.

Conclusions: The data suggest that increasing knowledge of this condition may shorten time to diagnosis. Use of the Bristol diagnostic criteria by an experienced clinician may obviate the need for biopsy in some patients.

Keywords: Autoinflammatory; Chronic recurrent multifocal osteomyelitis (CNO); Chronic recurrent non-bacterial osteomyelitis (CRMO); Cohort; Pamidronate.

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Figures

Fig. 1
Fig. 1
Correlation plots between interval between onset of symptoms and year of diagnosis for all 41 patients. R = −0.29
Fig. 2
Fig. 2
Bristol diagnostic criteria for CRMO

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