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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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Chronic recurrent multifocal osteomyelitis in a patient with selective immunoglobulin M deficiency

TL;DR: A case of a chronic recurrent multifocal osteomyelitis coexisting with selective IgM deficiency is reported, which can be associated with autoimmune diseases such as systemic lupus erythematosus, Hashimoto's disease, or hemolytic anemia.
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Osteomielitis crónica multifocal recurrente

TL;DR: Ahead of time, una revision retrospectiva de las historias clinicas de 5 pacientes con diagnostico de osteomielitis cronica multifocal recurrente de una consulta de infecciosas de un hospital terciario revela que existen nuevas alternativas de tratamiento.
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Chronic multifocal osteomyelitis: is infectious causation a moot point?

TL;DR: The potential for direct infectious causation or indirect causation by infectious stimulation of immunity cannot be entirely excluded and Infection as a mechanism for pathogenesis must continue to be entertained.
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Non-bacterial chronic osteomyelitis: experience in a tertiary hospital

TL;DR: The series, although limited, confirms the effectiveness and safety of bisphosphonate and anti-TNF therapy for children with NBCO.
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Normophosphatemic type tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis: a case report

TL;DR: A patient who developed tumoral calcinosis after the surgical treatment of CRMO is reported, which is the third patient in whom tumoral Calcinosis developed sporadically during follow-up for CRMO.
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).
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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.
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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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