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Infantile digital fibromatosis - a case report
P T Chirayil1, J Jayaraj, P Kumar
1Department of Burns and Plastic Surgery, Kasturba Medical College, Manipal 576 119, Karnataka, India.
Burns : Journal of the International Society for Burn Injuries
|February 13, 2001
Summary
Infantile digital fibromatosis (IDF) is a rare, non-malignant childhood tumor. Early recognition is key, as these lesions often resolve spontaneously without intervention.
Area of Science:
- Dermatology
- Pediatric Pathology
Background:
- Infantile digital fibromatosis (IDF), also known as Reye's tumor, is a rare, benign neoplastic proliferation.
- Typically affecting the digits of infants and children, IDF can also rarely occur in adults or the oral cavity.
Observation:
- This case report details an instance of congenital infantile digital fibromatosis on the right second toe.
- The lesion presented clinically with characteristics resembling a keloid.
Findings:
- Infantile digital fibromatosis is characterized by its common occurrence in childhood, often presenting at birth or within the first two years of life.
- Recurrence after surgical removal is noted, highlighting the importance of accurate diagnosis and management strategies.
Implications:
- Prompt recognition of infantile digital fibromatosis is crucial, as spontaneous regression is a known phenomenon.
- Understanding the clinical presentation and natural history of IDF aids in appropriate patient management and avoids unnecessary interventions.