Cahir John G, Toms Andoni P
Department of Radiology, Norfolk and Norwich University Hospital, Norfolk NR4 7UY, United Kingdom.
Eur J Radiol. 2008 Jul;67(1):2-10. doi: 10.1016/j.ejrad.2008.01.051. Epub 2008 Mar 20.
Regional migratory osteoporosis (RMO) is an uncommon disease characterised by a migrating arthralgia involving the weight bearing joints of the lower limb. The typical imaging findings on radiographs, magnetic resonance imaging, computed tomography and bone scintigraphy are described and illustrated. Men in their fifth and sixth decades of life are most commonly affected. The most common presentation is with proximal to distal spread in the lower limb. The world literature has been reviewed which has revealed 63 documented cases of regional osteoporosis or bone marrow oedema with migratory symptoms. Most of these cases have not been labelled as RMO and therefore the condition is probably under-diagnosed. The radiology of RMO is indistinguishable from transient osteoporosis of the hip (TOH) except for the migratory symptoms and the two conditions are likely to be part of the same spectrum of disease. Systemic osteoporosis is a more recently recognised accompanying feature that hints at an underlying aetiology and an approach to the management of this condition.
区域性迁移性骨质疏松症(RMO)是一种罕见疾病,其特征为累及下肢负重关节的游走性关节痛。文中描述并展示了X线片、磁共振成像、计算机断层扫描及骨闪烁显像的典型影像学表现。最常受累的是50和60多岁的男性。最常见的表现是下肢从近端向远端发展。回顾了世界文献,发现有63例记录在案的区域性骨质疏松症或伴有游走症状的骨髓水肿病例。其中大多数病例未被诊断为RMO,因此该病可能诊断不足。除了游走症状外,RMO的放射学表现与髋部暂时性骨质疏松症(TOH)无法区分,这两种情况可能是同一疾病谱的一部分。全身性骨质疏松症是最近才认识到的伴随特征,这提示了潜在的病因及该疾病的管理方法。