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Published on: April 12, 2019
Osteoid osteoma of phalangeal bone
Dennis S N Tsang1, Der-Yang Wu
1Division of Orthopedics, Cathay General Hospital, Taipei, Taiwan.
Summary
Osteoid osteomas in finger and toe bones are rare. Surgical excision offers a successful and complete cure for these rare bone tumors, with no recurrence reported in long-term follow-ups.
Area of Science:
- Orthopedic Surgery
- Oncology
- Radiology
Background:
- Osteoid osteoma is a benign bone tumor typically affecting long bones.
- Phalangeal involvement of the hands and feet is exceptionally rare.
Observation:
- Two cases of phalangeal osteoid osteoma are presented: one in a finger and one in a toe.
- Patients experienced prolonged symptoms including tenderness, swelling, and pain.
Findings:
- Both patients underwent successful surgical excision of the osteoid osteoma.
- Complete symptom relief was achieved post-surgery.
- Long-term follow-up (5 and 11 years) showed no recurrence or complications.
Implications:
- Surgical excision is the recommended treatment for phalangeal osteoid osteomas.
- Early diagnosis and surgical intervention can lead to excellent outcomes.
- This approach is particularly effective for accessible tumors in small bones.
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