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Congenital granular cell tumor in newborn
Tamer Zerener1, Metin Sencimen1, Ceyhan Altun2
1Departments of Oral and Maxillofacial Surgery, Center of Dental Sciences, Gulhane Medical Academy, Ankara, Turkiye.
European Journal of Dentistry
|June 17, 2014
Summary
Congenital granular cell tumor (CGCT) is a rare oral lesion in infants. Surgical removal is effective for this benign tumor, ensuring satisfactory healing.
Area of Science:
- Pediatric Dentistry
- Oral Pathology
- Oncology
Background:
- Congenital granular cell tumor (CGCT) is an exceptionally rare condition in newborns.
- Oral cavity lesions in infants require prompt diagnosis and management.
Observation:
- A 2-day-old female newborn presented with a smooth, non-fixated, pedunculated mass on the anterior mandibular alveolar ridge.
- The lesion measured 1 cm × 1 cm × 1.8 cm and originated from the gingival mucosa.
Findings:
- Histopathological evaluation confirmed the diagnosis of congenital granular cell tumor.
- The tumor was surgically excised on the seventh postnatal day under general anesthesia.
Implications:
- CGCT, though rare, is a treatable benign oral lesion in infants.
- Early surgical intervention leads to satisfactory post-operative recovery and healing.
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