Hu Y W, Liu R, Luo L
Department of Rheumatology, the First Affiliated Hospital of Xinjiang Medical University, Urumchi 8300542, China.
Department of Rheumatology, Peking University Third Hospital, Beijing 100191, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Dec 18;52(6):1140-1145. doi: 10.19723/j.issn.1671-167X.2020.06.026.
A case of chronic multifocal osteomyelitis was described in terms of its clinical manifestations, serological and imaging examinations, diagnostic criteria, treatment options, and follow-up evaluation after discharge. The pathogenesis, diagnosis, differential diagnosis and treatment of chronic multifocal osteomyelitis were reviewed, and the characteristics of autoinflammatory osteopathy were reviewed. The patient with onset from youth had developed severe skin lesions, progressive arthralgia and rachialgia. The clinical manifestation and the auxiliary examination of the patient accorded with the diagnosis of chronic multifocal osteomyelitis. After poor anti-inflammatory and analgesic effects, the switch to tumor necrosis factor alpha (TNF-α) inhibitor resulted in pain relief, normalization of inflammation indexes, and significant improvement in rash and imaging examination. Chronic recurrent multifocal osteomyelitis was a kind of autoinflammatory bone disease of multiple genes in disease with low incidence, unknown mechanism and unified diagnostic criteria. It was also known as chronic nonbacterial osteomyelitis, which was a rare, noninfectious inflammatory disorder that caused multifocallytic bone lesions characterized by periodic exacerbations and remissions. The exact pathophysiology or mechanism of the sterile bone inflammation was poorly understood, although chronic nonbacterial osteomyelitis was probably an osteoclast-mediated disease. In addition, an imbalance between pro- and anti-inflammatory cytokines was suspected to play a role. The available data so far pointed to the interplay among genetics, environmental, and immunologic factors as the causes of chronic nonbacterial osteomyelitis. Infectious etiology did not seem to play a crucial role in the pathogenesis of chronic nonbacterial osteomyelitis. It was often confused with metabolic bone disease, infection, tumor and other diseases. Its clinical manifestations were bone pain, fever, rash, fracture and so on. Laboratory examination showed significant increase in inflammatory markers. Radiographic examination revealed osteolytic or sclerosing changes. Magnetic resonance imaging was very useful for identifying bone lesions and tissue edema and was more accurate than bone emission computed tomography (ECT). Most of the patients begin to use non-steroidal anti-inflammatory drugs (NSAIDs) for treatment, but they are prone to relapse and new lesions appear. Other treatment options can be selected, including glucocorticoids, TNF-α inhibitors, bisphosphonates, methotrexate and other disease-modifying anti-rheumatic drugs (DMARDs). Early diagnosis and treatment can prevent and reduce complications and improve prognosis.
本文描述了一例慢性多灶性骨髓炎患者的临床表现、血清学及影像学检查、诊断标准、治疗方案以及出院后的随访评估。回顾了慢性多灶性骨髓炎的发病机制、诊断、鉴别诊断及治疗,并对自身炎症性骨病的特点进行了综述。该患者自幼起病,出现严重皮肤损害、进行性关节痛和腰痛。患者的临床表现及辅助检查符合慢性多灶性骨髓炎的诊断。在抗炎镇痛效果不佳后,改用肿瘤坏死因子α(TNF-α)抑制剂治疗,疼痛缓解,炎症指标恢复正常,皮疹及影像学检查有显著改善。慢性复发性多灶性骨髓炎是一种多基因自身炎症性骨病,发病率低,发病机制不明,诊断标准不统一。它也被称为慢性非细菌性骨髓炎,是一种罕见的非感染性炎症性疾病,可引起多灶性溶骨性骨病变,其特点是周期性加重和缓解。尽管慢性非细菌性骨髓炎可能是一种破骨细胞介导的疾病,但无菌性骨炎症的确切病理生理学或机制尚不清楚。此外,怀疑促炎细胞因子和抗炎细胞因子之间的失衡起了作用。目前可得的数据表明,遗传、环境和免疫因素之间的相互作用是慢性非细菌性骨髓炎的病因。感染性病因在慢性非细菌性骨髓炎的发病机制中似乎不起关键作用。它常与代谢性骨病、感染、肿瘤等疾病相混淆。其临床表现为骨痛、发热、皮疹、骨折等。实验室检查显示炎症标志物显著升高。影像学检查显示溶骨或硬化改变。磁共振成像对于识别骨病变和组织水肿非常有用,且比骨发射计算机断层扫描(ECT)更准确。大多数患者开始使用非甾体抗炎药(NSAIDs)治疗,但易复发且会出现新病变。可选择其他治疗方案,包括糖皮质激素、TNF-α抑制剂、双膦酸盐、甲氨蝶呤及其他改善病情抗风湿药(DMARDs)。早期诊断和治疗可预防和减少并发症,改善预后。