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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

Clinical outcome in children with chronic recurrent multifocal osteomyelitis

TL;DR: Clinical outcome of children with CRMO is generally good, but a sizeable proportion of patients have active disease at follow-up, and a minority of patients can have a severe and prolonged disease course despite intensive treatments.
Journal ArticleDOI

Chronic recurrent multifocal osteomyelitis: a concise review and genetic update.

TL;DR: The need to validate diagnostic clinical criteria and develop new pathogenesis-based targeted therapy is emphasized, as several observations suggest the contribution of genetic factors to the etiology of chronic recurrent multifocal osteomyelitis.
Journal ArticleDOI

Chronic recurrent multifocal osteomyelitis (CRMO): a longitudinal case series review

TL;DR: Chronic recurrent multifocal osteomyelitis is a polymorphous disorder in which whole-body MRI is extremely useful for showing subclinical edema and noninvasive diagnostic strategy is proposed.
Journal ArticleDOI

Autoinflammatory bone disorders.

TL;DR: In this overview CNO and Majeed syndrome, cherubism, hypophosphatasia and primary hypertrophic osteoarthropathy will be discussed, and a genetic cause affecting bone metabolism and leading to chronic bone inflammation has been described.
Journal ArticleDOI

Chronic recurrent multifocal osteomyelitis: review.

TL;DR: Chronic recurrent multifocal osteomyelitis can be a difficult diagnosis, often with nonspecific imaging findings, and the critical factors leading to its diagnosis are patient demographics, clinical course, and distribution.
References
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Journal Article

[Acne-pustulosis-hyperostosis-osteitis syndrome. Results of a national survey. 85 cases].

TL;DR: From this investigation, it appears that dermatological and osseous pictures described under various denominations, present common characteristics and transition forms justifying their common study under the acronym SAPHO (Syndrome Acne-Pustulosis-Hyperostosis-Osteitis).
Journal ArticleDOI

The SAPHO syndrome

TL;DR: The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is the cornerstone of this new syndrome, which also has links with spondyloarthropathies and plain psoriasis.
Journal ArticleDOI

Histopathological aspects of chronic recurrent multifocal osteomyelitis

TL;DR: Morphologically CRMO begins as an acute inflammatory process with a predominance of polymorphonuclear leucocytes, which occasionally form an abscess and osteoclastic bone resorption, but at a later stage the predominant features are lymphocytes in the inflammatory infiltrates and occasional granulomatous foci and sigans of bone formation.
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