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Cherubism in 12 Year Young Female
Heena Mazhar1, Ratna Samudrawar2, Rubi Gupta3
1Department of Oral and Maxillofacial Surgery, Chhattisgarh Dental College and Research Institute, Rajnandgaon, Chhattisgarh, India.
Annals of Maxillofacial Surgery
|January 30, 2019
Summary
Cherubism, a rare inherited jaw condition, typically resolves by puberty. This report details a nonfamilial case in a teenager, treated post-puberty with surgery after initial calcitonin therapy.
Area of Science:
- Oral and Maxillofacial Surgery
- Genetics
- Pediatric Dentistry
Background:
- Cherubism is a rare, benign, autosomal-dominant inherited fibro-osseous jaw lesion.
- Characterized by jaw bone degradation and fibrous tissue masses, it typically self-limits and involutes by puberty.
- This condition usually presents in early childhood.
Observation:
- A nonfamilial case of cherubism in a teenage female patient is presented.
- The patient initially received calcitonin nasal spray treatment.
- Surgical resection and recontouring were performed after puberty.
Findings:
- Cherubism management may require intervention beyond the typical pubertal involution period.
- Nonfamilial cases, though rare, necessitate tailored treatment approaches.
- Combined medical and surgical interventions can be effective for cherubism post-puberty.
Implications:
- This case highlights the potential need for extended management strategies for cherubism.
- It expands understanding of cherubism's clinical course and treatment in nonfamilial teenage cases.
- Further research into long-term outcomes of surgical and medical cherubism treatments is warranted.
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