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Caffey's disease: an unusual cause for concern
F J Shannon1, M Murphy, I Atchia
1Department of Orthopaedic Surgery, Our Ladys' Hospital for Sick Children, Crumlin, Dublin 12, Ireland. fjshannon@gmail.com
Caffey's disease, a rare cause of infantile bone pain, presents subtly with fever and tenderness. Diagnosis often requires skeletal surveys to identify characteristic cortical thickening, especially in infants.
Area of Science:
- Pediatric Radiology
- Neonatal Medicine
- Skeletal Dysplasias
Background:
- Caffey's disease, also known as infantile cortical hyperostosis, is a rare condition.
- It typically manifests in infants with irritability, bone pain, soft tissue swelling, and fever.
- Early recognition is crucial for appropriate management and to differentiate from other pediatric conditions.
Observation:
- An 8-week-old infant presented with focal tibial tenderness and pyrexia.
- Initial laboratory work-up yielded inconclusive results.
- Clinical suspicion prompted further investigation to rule out non-accidental injury.
Findings:
- A skeletal survey revealed characteristic cortical thickening in the mandible and tibia.
- These radiological findings confirmed the diagnosis of Caffey's disease.
- The diagnostic process highlighted the importance of comprehensive imaging.
Implications:
- Caffey's disease diagnosis relies heavily on radiographic evidence, particularly plain X-rays.
- The condition underscores the need for a broad differential diagnosis in infants presenting with bone pain.
- Increased immigration necessitates consideration of diverse etiologies in emergency room evaluations.
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