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骨炎和慢性复发性多灶性骨髓炎。

Bone inflammation and chronic recurrent multifocal osteomyelitis.

机构信息

Institute of Tissue Engineering and Stem Cells, Nanchong Central Hospital, Second Clinical Institute of North Sichuan Medical University, Nanchong, Sichuan, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Mar;22(5):1380-1386. doi: 10.26355/eurrev_201803_14482.

Abstract

Chronic recurrent multifocal osteomyelitis (CRMO) is a sporadic condition of inflammatory bone pain that occurs as recurrent flares because of osteomyelitis, which presents in the form of multiple aseptic foci. The estimated prevalence of CRMO is 1-2 per million, affecting mostly children, in the age group of 2 to 17. Main symptoms of CRMO are bone inflammation and pain, which are generally worse at night. Other symptoms seen on radiographs indicate osteolytic lesions surrounded by sclerosis, at later stages of the disease. Markers of inflammation, viz. tumor necrosis factor a and C-reactive protein are elevated in many cases. Because of similar symptoms, differential diagnosis is needed to confirm CRMO from infectious osteomyelitis, bone tumors, and other diseases. The genetic component is likely in some cases such as Majeed syndrome, deficiency of IL-1 antagonist, etc. Imaging is the essential part of diagnosing CRMO, and magnetic resonance imaging of the whole body is the most widely used and recommended method for the evaluation of multiple foci, as compared to radiography for reasons of sensitivity as well as prevention of excessive exposure of affected children to radiation. CRMO is considered an autoimmune and auto-inflammatory disorder, but its precise pathophysiology is not clear. Current treatment options are non-steroid anti-inflammatory drugs like naproxen, as the primary choice, and the bisphosphonates such as pamidronate as the second choice, to counter the symptoms and to reduce bone lesions. The surgical option is the choice for recalcitrant cases, even though recurrence may still be a problem.

摘要

慢性复发性多灶性骨髓炎(CRMO)是一种散发性炎症性骨痛疾病,由于骨髓炎反复发作,呈多发性无菌性病灶,表现为复发性发作。CRMO 的估计患病率为每百万人口 1-2 人,主要影响儿童,年龄在 2 至 17 岁之间。CRMO 的主要症状是骨炎症和疼痛,通常在夜间更严重。在疾病的后期,放射照片上显示的其他症状表明溶骨性病变伴有硬化,在疾病的后期。许多情况下炎症标志物,如肿瘤坏死因子 a 和 C 反应蛋白升高。由于症状相似,需要进行鉴别诊断以确认 CRMO 与感染性骨髓炎、骨肿瘤和其他疾病。在某些情况下,如 Majeed 综合征、白细胞介素-1 拮抗剂缺乏等,遗传因素可能起作用。影像学是诊断 CRMO 的重要组成部分,全身磁共振成像(MRI)是评估多发病灶最广泛使用和推荐的方法,与放射照相相比,其原因是敏感性以及避免受影响儿童过度暴露于辐射。CRMO 被认为是一种自身免疫和自身炎症性疾病,但确切的病理生理学尚不清楚。目前的治疗选择是非甾体抗炎药,如萘普生,作为首选,双膦酸盐,如帕米膦酸,作为二线选择,以缓解症状和减少骨病变。手术选择是难治性病例的选择,尽管仍可能存在复发问题。

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