Journal of Peking University (Health Sciences) ›› 2020, Vol. 52 ›› Issue (6): 1140-1145. doi: 10.19723/j.issn.1671-167X.2020.06.026

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Chronic multifocal osteomyelitis: A case report and literature review

Yong-wei HU1,Rui LIU2,(),Li LUO1,()   

  1. 1. Department of Rheumatology, the First Affiliated Hospital of Xinjiang Medical University, Urumchi 8300542, China
    2. Department of Rheumatology, Peking University Third Hospital, Beijing 100191, China
  • Received:2020-07-31 Online:2020-12-18 Published:2020-12-13
  • Contact: Rui LIU,Li LUO E-mail:maryllr@163.com;luoli.6@163.com

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Abstract:

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.

Key words: Chronic multifocal osteomyelitis, Inflammatory osteopathy, Tumor necrosis factor-alpha inhibitors

CLC Number: 

  • R681.2

Figure 1

MRI of sacroiliac joint before and after treatment A and B, T2 weighted image suggested sacroiliac bone marrow edema (the red arrows) before treatment; C and D, after 10 weeks of treatment, the bone marrow edema (the red arrows) of sacroiliac joint was significantly improved."

Figure 2

Acne on the head, face, neck, and back of the patient"

Figure 3

CT of sacroiliac joint"

Figure 4

MRI of spinal before and after treatment 4A-C, before the treatment, multiple vertebral keratositis and endplate inflammation were found in spine, and bone marrow edema (the red arrows) at the junction of sternum body and sternal stalk could be seen; 4D and 4E, after 10 weeks of treatment, spinal bone marrow edema was significantly improved."

Figure 5

Bone ECT"

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