Chronic recurrent multifocal osteomyelitis

Citation
F. Schilling et S. Kessler, Chronic recurrent multifocal osteomyelitis, KLIN PADIAT, 213(5), 2001, pp. 271-276
Citations number
35
Categorie Soggetti
Pediatrics
Journal title
KLINISCHE PADIATRIE
ISSN journal
03008630 → ACNP
Volume
213
Issue
5
Year of publication
2001
Pages
271 - 276
Database
ISI
SICI code
0300-8630(200109/10)213:5<271:CRMO>2.0.ZU;2-K
Abstract
Juvenile and adolescent "Chronic Recurrent Multifocal Osteomyelitis" (CRMO) is described on the basis of literature and analysis of 43 own cases (23 c ases in children or adolescents). This systemic, non-purulent inflammatory disease occurs mainly metaphyseal in long bones, in pelvic bones or as spondylitis and is not as rare as it s eemed. Basis of the disease is a primarily chronic, sterile, in phase of on set often monotopic (e.g. clavicle) and later frequently polytopic osteomye litis, possibly triggered by an immuno-pathological process (e.g. Proprioni bacterium acnes), and showing histologically plasmacellular invasion and a sclerosing process in different stages. Association with pustulous dermatos is (psoriasis, acne, palmo-plantar pustulosis) is found in about 25% of chi ldren and adolescents and in more than 50% of the adult patients. 5 differe nts types of distribution of osteomyelitic lesions can be found by using Te 99m-bone scan primarily, of which the "pelvic type" is the most common. Bec ause of the close neighbourhood of meta-/epiphyseal osteomyelitic focuses, "sympathetic arthritis" with synovitis is seen frequently. A therapeutic ap proach with azithromycine and calcitonine is presented.