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[Paget's disease with an exclusively maxillary location. A case report]
1Divisione di Odontoiatria e Stomatologia, Ospedale Mauriziano Umberto I, Torino.
Minerva Stomatologica
|June 1, 1994
Summary
This case report details Paget's disease localized exclusively to the craniofacial region. Diagnosis was confirmed through imaging and histological examination of alveolar bone.
Area of Science:
- Osteology
- Pathology
- Radiology
Background:
- Paget's disease is an osteocondensing dystrophy characterized by excessive bone remodeling.
- This leads to bone hypertrophy, increased density, and vascularization, causing deformities and pain.
Observation:
- A 70-year-old patient presented with craniofacial Paget's disease after tooth extractions.
- Radiographic and histological analyses revealed significant bone remodeling in the maxilla and cranium.
Findings:
- Paget's disease confirmed via hematochemical tests, bone scintigraphy, and alveolar bone histology.
- The disease manifested with a mucous crater and bone involvement at the extraction site.
Implications:
- Highlights the importance of considering Paget's disease in craniofacial presentations, especially with dental complications.
- Early diagnosis through imaging and histology is crucial for managing this rare bone disorder.