Chronic Recurrent Multifocal Osteomyelitis (CRMO): The Deceptive Disease That Mimics Sarcoma Radiologically but Promises a Complete Recovery.

Sage open pathology Pub Date : 2025-01-23 eCollection Date: 2025-01-01 DOI:10.1177/30502098251314782
Lalani De Silva, Sunil Wijayasinghe, Chandu de Silva
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Abstract

Chronic recurrent multifocal osteomyelitis (CRMO) is a rare and distinct form of chronic non-bacterial osteomyelitis with an unknown etiology. This 11-year-old Asian girl presented with a painful swelling in her right arm, which was suspected to be a Ewing's sarcoma based on radiological findings. The lesion appeared as a unifocal destructive bone lesion in the proximal diaphyseal region of the right humerus, accompanied by periosteal reaction and soft tissue involvement. She was otherwise clinically well, except for the elevated C-reactive protein, erythrocyte sedimentation rate and alkaline phosphatase. Due to the clinical and radiological suspicion of sarcoma, repeated bone biopsies were performed. All the biopsies revealed mature lamellar bone, normocellular marrow with moderate mixed inflammation, and fibrosis, indicative of a chronic inflammatory process. Given the discordance between the clinical, radiological, and pathological findings, surgical management was withheld and the patient was closely monitored. Over the course of several months, her symptoms gradually improved without any medical or surgical interventions. A follow-up X-ray taken 3 years after the initial diagnosis showed that the lesion had significantly reduced in size, nearly returning to a normal bone contour.

慢性复发性多灶性骨髓炎(CRMO):一种具有欺骗性的疾病,放射学上类似肉瘤,但承诺完全恢复。
慢性复发性多灶性骨髓炎(CRMO)是一种罕见而独特的慢性非细菌性骨髓炎,病因不明。这个11岁的亚洲女孩表现为右臂疼痛肿胀,根据放射检查结果怀疑是尤因氏肉瘤。病变表现为右肱骨干近端单灶性破坏性骨病变,伴有骨膜反应和软组织受累。除了c反应蛋白、红细胞沉降率和碱性磷酸酶升高外,其他临床表现良好。由于临床和影像学怀疑为肉瘤,多次行骨活检。所有活检显示成熟板层骨,正常细胞骨髓伴中度混合炎症和纤维化,表明慢性炎症过程。鉴于临床,放射学和病理结果之间的不一致,手术治疗被保留,患者被密切监测。在几个月的过程中,她的症状逐渐改善,没有任何药物或手术干预。初次诊断3年后的随访x线显示病变的大小明显减小,几乎恢复到正常的骨轮廓。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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