Chronic recurrent multifocal osteomyelitis.

Citation
F. Schilling et al., Chronic recurrent multifocal osteomyelitis., Z ORTHOP GR, 138(6), 2000, pp. 530-539
Citations number
80
Categorie Soggetti
Ortopedics, Rehabilitation & Sport Medicine
Journal title
ZEITSCHRIFT FUR ORTHOPADIE UND IHRE GRENZGEBIETE
ISSN journal
00443220 → ACNP
Volume
138
Issue
6
Year of publication
2000
Pages
530 - 539
Database
ISI
SICI code
0044-3220(200011/12)138:6<530:CRMO>2.0.ZU;2-L
Abstract
The aim of this paper is to give a detailed description of the so-called "c hronic recurrent multifocal osteomyelitis" (CRMO). The clinical, radiologic al and histopathological results of an analysis of 29 cases (15 children/ad olescents and 14 adults) are presented and correlated to current data from the literature. We could delinate the following points: 1. CRMO is a system ic aseptic inflammation of the bone marrow (Osteitis), it can occur polytop ically and association with pustulous dermatologic symptoms is possible. 2. It is not a rare disease! 3. Osteomyelitis is probably "reactive" and a pl asma-cell sclerotic process with ist own characteristic histologic three-ph ase course. 4. We could observe 5 specific types of localization which can be documented by X-ray or bone scan. 5. Accompanying arthritis os often pre sent, especially "sympathetic coxitis". 6. The use of drugs in treatment of CRMO (i.e. azithromycin, calcitonin, and bisphosphonates) is discussed. In conclusion we want to point out, that 1. (TC)-T-99m bone scan should alway s be performed when there is suspicion for CRMO to reveal the pattern of af fection, 2. the rheumatologist and dermatologist should be contacted, 3. op eration is normally not necessary for treatment of the mostly self-limitin disease, and 4. the term "SAPHO syndrome" should be avoided, further differ entiation of the diagnosis is necessary.