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Juvenile-onset multifocal osteonecrosis in systemic lupus erythematosus

机译:少年发病的多焦点骨质骨折在全身狼疮红斑狼疮

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RATIONALE:Osteonecrosis (ON) is a devastating illness that leads to bone ischemia and potential joint destruction. Systemic lupus erythematosus (SLE) is a chronic, autoimmune disease, with multi-system involvement which is closely associated with occurrence of ON. Multifocal ON, with an estimated morbidity of 3% in SLE patients, is extremely rare in juvenile subjects.PATIENT CONCERNS:A 13.3-year-old female SLE patient was admitted to hospital 20 months following the SLE diagnosis because of a sudden aggravation of sore knees. She suffered from double knee joint pain and her left knee joint showed typical signs of inflammation including redness, swelling, heat, and pain.DIAGNOSES:The SLE patient was diagnosed with multifocal ON of her knee joint based on magnetic resonance imaging findings of bone destruction and osteoproliferation at the bilateral distal femur and proximal tibia.INTERVENTIONS:The patient received high-dose methylprednisolone and intravenous cyclophosphamide pulse therapies for controlling active lupus and nephritis. Oral calcitriol and dipyridamole were administered to alleviate knee pain and inhibit thrombi formation, thereby suppressing ON progress.OUTCOMES:Three weeks following the treatment, the swelling in patient's left knee subsided. Her self-reporting pain score decreased from 9 to 4 and walking time increased from 45minutes to 90minutes per day. Nearly 5 weeks later, the pain in bilateral knee joints disappeared and the patient could walk without difficulties.LESSONS:This patient is the youngest SLE patient who developed multifocal ON based on the reported literature. It suggests that ON can occur in young SLE patients. A combination of internal and external risk factors can promote the development of ON. The balanced approach to the application of corticosteroids and immunosuppressors in the treatment of SLE and prevention of ON is a challenging problem that deserves further exploration.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:理由:骨坏死(ON)是一种破坏性的疾病,导致骨缺血和潜在的关节破坏。 Systemic Lupus红斑(SLE)是一种慢性自身免疫性疾病,具有多系统的参与,与发生的发生密切相关。多焦点ON,SLE患者的估计发病率为3%,在少年受试者中极为罕见。患病问题:由于突然加剧疼痛,13.3岁的女性SLE患者入院20个月后入院膝盖。她患有双膝关节疼痛,她的左膝关节显示出典型的炎症迹象,包括发红,肿胀,热量和疼痛。诊断为SLE患者基于骨破坏的磁共振成像结果诊断出膝关节的多焦点上双侧远端股骨和近端胫骨的骨升迁。Interventions:患者接受高剂量的甲基己酮和静脉内环磷酰胺脉冲验疗,用于控制活性狼疮和肾炎。施用口服钙二醇和双嘧达莫抑制膝关节疼痛并抑制血栓形成,从而抑制进展。待遇:治疗后三周,患者左膝部肿胀消退。她自报的疼痛评分从9下降到4,步行时间从45分钟增加到每天90分钟。近5周后,双边膝关节的疼痛消失,患者可以毫无困难地走路:这个患者是基于报告的文学开发多焦点的最年轻的SLE患者。它表明,在年轻的SLE患者中可能发生。内部和外部危险因素的组合可以促进开发。皮质类固醇和免疫抑制剂在治疗SLE和预防下施用皮质类固醇和免疫压缩机的平衡方法是一个挑战性的问题,值得进一步的探索.Copyright? 2021提交人。由Wolters Kluwer Health,Inc。出版

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