Bouvier M, Liens D, Tebib J G, Noel E
Centre hospitalier Lyon-Sud, Pierre Benite.
Ann Radiol (Paris). 1993;36(4):293-302.
Based on a series of eight personal cases and a review of the literature, this study tries to define the diagnostic elements of aseptic osteomyelitis. Although sternocostoclavicular sites are immediately suggestive of the diagnosis, lesions of the pelvis and spine and long bones of the limbs are particularly difficult to diagnose. Inflammatory type pain occurred in episodesover a number of years and responded to NSAIs and possibly diphosphonates. Laboratory abnormalities were usually confined to a raised ESR, but alterations of the IgA levels, similar to those observed in ankylosing spondylitis were observed in four cases. Hyperostosis occurred late in the course, preceded by signs of osteomyelitis, periosteitis or enthesitis. Histology does not provide any formal conclusions. The most suggestive lesions are those of nonspecific aseptic osteomyelitis, followed by a Paget-like appearance. The interpretation of these findings may be complicated by the presence of eosinophils, giant cells or mast cells. Two elements are very valuable for establishing the diagnosis: the presence of infraradiological anterior thoracic increased uptake on bone scan and the presence of a skin disorder, either severe acne or, more especially, palmoplantar pustulosis.
基于一系列8例个人病例及文献回顾,本研究试图明确无菌性骨髓炎的诊断要素。虽然胸锁关节部位可立即提示诊断,但骨盆、脊柱及四肢长骨的病变特别难以诊断。炎症性疼痛呈数年发作,对非甾体抗炎药及可能对双膦酸盐有反应。实验室异常通常局限于血沉升高,但4例患者观察到与强直性脊柱炎中所见相似的IgA水平改变。骨肥厚在病程后期出现,之前有骨髓炎、骨膜炎或附着点炎的迹象。组织学检查未得出任何明确结论。最具提示性的病变是非特异性无菌性骨髓炎的病变,其次是类似佩吉特病的表现。嗜酸性粒细胞、巨细胞或肥大细胞的存在可能会使这些发现的解读变得复杂。对于确立诊断有两个非常有价值的要素:骨扫描显示放射线下前胸摄取增加以及存在皮肤疾病,即重度痤疮或更常见的掌跖脓疱病。