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Extra-osseous manifestations in chronic recurrent multifocal osteomyelitis: a retrospective study
Marie Robert1,2, Anna Giolito1,2, Heloise Reumaux3
1Service de Rhumatologie Pédiatrique, Centre de Référence des Maladies Auto-Inflammatoires et des Amyloses Inflammatoires (CEREMAIA), Hôpital Bicêtre, Assistance Publique-Hôpitaux de Paris (AP-HP), Le Kremlin-Bicêtre, France.
Extra-osseous manifestations affect two-thirds of chronic recurrent multifocal osteomyelitis (CRMO) patients, often requiring biologic therapy. Understanding these CRMO phenotypes is key for tailored management.
Area of Science:
- Pediatric Rheumatology
- Osteomyelitis Research
- Inflammatory Diseases
Background:
- Chronic recurrent multifocal osteomyelitis (CRMO) is a rare autoinflammatory bone disease.
- Extra-osseous (EO) manifestations in CRMO are not well-defined.
- Characterizing EO events is crucial for understanding CRMO heterogeneity.
Purpose of the Study:
- To determine the frequency and characteristics of EO manifestations in CRMO.
- To investigate treatment patterns for CRMO with EO involvement.
- To identify distinct CRMO phenotypes based on EO manifestations.
Main Methods:
- Multicentre retrospective study of CRMO patients (2015-2022).
- EO manifestations included skin, gastrointestinal, joint, and systemic symptoms.
- Data collected on demographics, clinical features, and treatments.
Main Results:
- EO manifestations occurred in 67.7% of 133 CRMO patients.
- Predominant EO symptoms were skin lesions (56.7%) and sacroiliitis (42.2%).
- Patients with EO manifestations more frequently received biologics (36.7% received TNF inhibitors).
Conclusions:
- CRMO patient cohorts can be delineated into distinct groups based on EO involvement.
- Biologic therapies, particularly TNF inhibitors, show promise in managing CRMO with EO manifestations.
- Further research into CRMO pathophysiology may reveal underlying mechanisms for diverse phenotypes.
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