F. Schilling, CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITI S (CRMO), RoFo. Fortschritte auf dem Gebiete der Rontgenstrahlen und der neuenbildgebenden Verfahren, 168(2), 1998, pp. 115-127
Citations number
98
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
Journal title
RoFo. Fortschritte auf dem Gebiete der Rontgenstrahlen und der neuenbildgebenden Verfahren
Chronic recurrent multifocal osteomyelitis (CRMO) is an unusual clinic
al entity. More than 200 cases are described in the literature and it
is presented here with special reference to its radiological aspects.
It is an acquired disease of the skeleton which occurs predominantly d
uring childhood and adolescence. About ten per cent of cases begin in
early or, rarely, in later adult life. This variant is described here
for the first time and is discussed as ''adult CRMO''. The underlying
pathology is a bland, predominantly lympho-plasma cellular osteomyelit
is which is self-limiting and leads to bone sclerosis (Garre). It prob
ably involves an abnormal immune process which follows an infection bu
t remains clinically latent and remains aseptic and sterile. In a quar
ter of cases there is an association with pustulosis palmo-plantaris a
nd its relationship with psoriatic arthropathy is discussed. The clini
cal, histopathological and imaging features (radiological and particul
arly MRT) and the bone changes are described. This provides a spectrum
of symptoms; the radiological differential diagnosis and the relation
ship with hyperostotic spondyloarthroses during adult life are discuss
ed. The relationship between CRMO, the SAPHO syndrome and acquired hyp
erostosis syndrome are analysed.