Chronic recurrent multifocal osteomyelitis

被引:23
|
作者
Schilling, F [1 ]
Kessler, S [1 ]
机构
[1] Univ Mainz Klinikum, Rheinland Pfalz Rheumazentrum Mainz Bad Kreuznach, Mainz, Germany
来源
KLINISCHE PADIATRIE | 2001年 / 213卷 / 05期
关键词
chronic recurrent multifocal osteomyelitis; primarily chronic osteomyelitis; lymphoplasmacellular osteomyelitis; sclerosing osteomyelitis (Garre); sympathetic osteomyelitis; SAPHO-syndrome; acithromycine;
D O I
10.1055/s-2001-17218
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Juvenile and adolescent "Chronic Recurrent Multifocal Osteomyelitis" (CRMO) is described on the basis of literature and analysis of 43 own cases (23 cases 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 seemed. Basis of the disease is a primarily chronic, sterile, in phase of onset often monotopic (e.g. clavicle) and later frequently polytopic osteomyelitis, possibly triggered by an immuno-pathological process (e.g. Proprionibacterium acnes), and showing histologically plasmacellular invasion and a sclerosing process in different stages. Association with pustulous dermatosis (psoriasis, acne, palmo-plantar pustulosis) is found in about 25% of children and adolescents and in more than 50% of the adult patients. 5 differents types of distribution of osteomyelitic lesions can be found by using Te99m-bone scan primarily, of which the "pelvic type" is the most common. Because of the close neighbourhood of meta-/epiphyseal osteomyelitic focuses, "sympathetic arthritis" with synovitis is seen frequently. A therapeutic approach with azithromycine and calcitonine is presented.
引用
收藏
页码:271 / 276
页数:6
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