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Chronic recurrent multifocal osteomyelitis in association with pyoderma gangraenosum
Matthias Christian Wurm1, Ines Brecht2, Michael Lell3
1Department of Oral and Maxillofacial Surgery, University of Erlangen-Nürnberg, Glückstrasse 11, 91054, Erlangen, Germany. Matthias.Wurm@uk-erlangen.de.
BMC Oral Health
|September 3, 2016
Summary
Chronic recurrent multifocal osteomyelitis (CRMO), a rare inflammatory bone disorder, can manifest unusually. This case highlights CRMO affecting the mandible, presenting a diagnostic challenge due to its rarity.
Area of Science:
- Pediatric Rheumatology
- Skeletal Dysplasias
- Inflammatory Disorders
Background:
- Chronic recurrent multifocal osteomyelitis (CRMO) is a rare, acquired inflammatory skeletal disorder of unknown origin.
- CRMO primarily affects children and young adults, predominantly females, characterized by relapsing-remitting courses.
- Typically, CRMO affects long bones' metaphysis, presenting as painful swellings.
Observation:
- A 14-year-old female presented with escalating neck pain and facial swelling, recurring quarterly for four years.
- Clinical examination revealed moderately elevated C-reactive protein (CRP) and an increased blood sedimentation rate (BSR).
- Radiographic imaging identified a bone alteration in the left mandibular region.
Findings:
- The case report details an unusual presentation of CRMO involving the mandible.
- This mandibular CRMO was associated with pyoderma gangraenosum.
- Diagnostic investigations confirmed CRMO as the cause of the mandibular lesion.
Implications:
- Rare diseases can present with exceptionally uncommon symptoms, posing significant diagnostic challenges.
- This case underscores the importance of considering CRMO in pediatric patients with unexplained mandibular lesions and inflammatory markers.
- Increased awareness of atypical CRMO presentations is crucial for timely diagnosis and management.
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