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Chronic recurrent multifocal osteomyelitis in children

TLDR
It has been shown that histological examination alone does not allow the distinction of CRMO from acute or subacute bacterial osteomyelitis, therefore an extensive microbial workup of the tissue biopsy, including PCRtechniques, is essential in order to establish the diagnosis and decide as to the treatment.
Abstract
Chronic recurrent multifocal osteomyelitis (CRMO) in children is an inflammatory disorder. It affects mainly the metaphyses of the long bones, in addition to the spine, the pelvis and the shoulder girdle. However, bone lesions can occur at any site of the skeleton. Even though this disease has been recognized as a clinical entity for almost three decades now, its origin and pathogenesis are not entirely clear. No apparent infectious agents are detectable at the site of the bone lesion. No epidemiological data on incidence and prevalence have been published so far. However, incidence might be something around 1:1,000,000, thus reflecting the number of patients followed-up. Clinical diagnosis in an affected child can be difficult because the clinical picture and course of disease may vary significantly. It has been shown that histological examination alone does not allow the distinction of CRMO from acute or subacute bacterial osteomyelitis. Therefore an extensive microbial workup of the tissue biopsy, including PCRtechniques, is essential in order to establish the diagnosis and decide as to the treatment. Non steroid anti-inflammatory drugs (NSAID) are the treatment of choice. In case of frequent relapses oral steroid treatment, bisphosphonates and azulfidine have been used and are reported to be beneficial.

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Citations
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Journal ArticleDOI

Chronic non-bacterial osteomyelitis in children

TL;DR: CNO is a spectrum of inflammatory conditions, with CRMO being the most severe, but most children with CNO have a favourable outcome of the disease.
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Dramatic pain relief and resolution of bone inflammation following pamidronate in 9 pediatric patients with persistent chronic recurrent multifocal osteomyelitis (CRMO)

TL;DR: Pamidronate resulted in resolution of pain and MRI documented inflammation in all patients and it is proposed that pamidronsate is an effective second-line therapy in persistent CRMO.
Journal ArticleDOI

Synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome in childhood: a report of ten cases and review of the literature.

TL;DR: The synovitis, acne, pustulosis, hyperostosis, osteitis syndrome is pertinent even in paediatrics since skin involvement is frequent, and in adults, chronic recurrent multifocal osteomyelitis is now a classical manifestation of SAPHO syndrome.
Journal ArticleDOI

Current Understanding of the Pathogenesis and Management of Chronic Recurrent Multifocal Osteomyelitis

TL;DR: There is a strong association with inflammatory disorders of the skin and intestinal tract in affected individuals and their close relatives, suggesting a shared pathophysiology and supporting a genetic component to disease susceptibility.
Journal ArticleDOI

Chronic Recurrent Multifocal Osteomyelitis

TL;DR: Non-steroidal anti-inflammatory drugs cause relief of symptoms in the majority of cases and Bisphosphonates and TNF-α blockers are alternatives for patients who do not respond or who have spinal involvement.
References
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Journal ArticleDOI

Chronic recurrent multifocal osteomyelitis: five-year outcomes in 14 pediatric cases.

TL;DR: As compared to SAPHO syndrome, skin lesions and chest wall involvement are less common in CRMO and the long-term prognosis is guarded: in this study only six of 14 patients were in remission at last follow-up.
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Chronic recurrent multifocal osteomyelitis in children: diagnostic value of histopathology and microbial testing

TL;DR: Histopathologic analysis of 12 patients with CRMO indicated a wide variation of reparative changes of bone, but chronic inflammation could not be found at all sites in the same biopsy, and CRMO should be included in the differential diagnosis of chronic inflammatory bone lesions in children.
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Evolution of chronic recurrent multifocal osteitis toward spondylarthropathy over the long term

TL;DR: After 10 years, CRMO had usually evolved to spondylarthropathy, but with certain features not usually seen in the latter: predominantly, unilateral sacroiliitis, no familial form, and no link with HLA-B27.
Journal ArticleDOI

Chronic multifocal osteomyelitis

TL;DR: Twenty-two patients who presented between the ages of 4 and 14 years with gradual onset of malaise and pain at the sites of multiple bone lesions were described, with no evidence of altered bone growth or abnormal joint development.
Journal ArticleDOI

Chronic recurrent multifocal osteomyelitis. Association with vertebra plana.

TL;DR: The natural history of chronic recurrent multifocal osteomyelitis appears to be slow, spontaneous resolution of the osseous lesions without specific treatment, and therapy with antibiotics can be withheld.
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