Chronic nonbacterial osteomyelitis may be associated with renal disease and bisphosphonates are a good option for the majority of patients. (24th April 2016)

• Record Type: Journal Article
• Authors: Pastore, Serena; Ferrara, Giovanna; Monasta, Lorenzo; Meini, Antonella; Cattalini, Marco; Martino, Silvana; Alessio, Maria; Torre, Francesco La; Teruzzi, Barbara; Gerloni, Valeria; Breda, Luciana; Taddio, Andrea; Lepore, Loredana
• Is Part Of: Acta pædiatrica. Volume 105:Number 7(2016)
• Page Start: e328
• Page End: e333
• Publication Date: 2016-04-24
• Subjects: Bisphosphonates -- Bone pain -- Children -- Chronic nonbacterial osteomyelitis -- Chronic recurrent multifocal osteomyelitis; Pediatrics -- Periodicals; Pediatrics; 618.92
• DOI: 10.1111/apa.13420
• Languages: English
• ISSNs: 0803-5253

Abstract

Abstract: Aim: The aim of this Italian study was to describe the clinical features, treatment options and outcomes of a cohort of patients with chronic nonbacterial osteomyelitis (CNO). Methods: This was a retrospective cohort study. Laboratory data, diagnostic imaging, histological features and clinical course are reported. Results: We enrolled 47 patients diagnosed with CNO. Bone pain was the leading symptom, and multifocal disease was present in 87% of the patients. The majority of the bone lesions were located in the appendicular skeleton (58%). Extraosseous manifestations were present in 34% of the patients, and renal involvement was detected in four patients. Inflammatory indices were increased in 80%, and bone x‐rays were negative in 15% of the patients. Nonsteroidal anti‐inflammatory drugs (NSAIDs) were the first therapy for all patients, achieving clinical remission in 27%. A good response to NSAIDs was significantly associated with a better prognosis. Bisphosphonates were used in 26 patients, with remission in 73%. Only six patients (13%), all with spine involvement, developed sequelae. Conclusion: We found a possible association between CNO and renal disease. Bisphosphonates were more likely to lead to clinical remission when NSAIDs and corticosteroids had failed. Vertebral localisation was the only risk factor for potential sequelae.