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Congenital epulis
O Lapid1, R Shaco-Levy, Y Krieger
1Department of Plastic Surgery, the Soroka University Medical Center Ben-Gurion University of the Negev, Negev, Israel. lapid@actcom.co.il
Insights
Epulis, a rare newborn tumor, presents as a gingival mass. Surgical resection is recommended, with no reported recurrences, indicating less radical excision may suffice.
Area of Science:
- Pediatric Oncology
- Oral Pathology
Background:
- Epulis, also known as granular cell tumor of the newborn or Neumann's tumor, is a rare congenital oral tumor.
- It typically presents as a gingival mass in newborns, potentially impacting respiration and feeding.
Observation:
- This study describes a newborn female with epulis.
- The tumor was successfully resected using a carbon dioxide laser with an uneventful postoperative course.
Findings:
- Histologic examination revealed polygonal cells with granular cytoplasm, positive for vimentin and negative for S100-protein and other markers.
- Electron microscopy showed granular cells with dense granules, lysosomes, and lipid droplets.
Implications:
- Epulis is a distinct entity in newborns, showing a strong female predilection (8:1).
- Prompt surgical resection is the standard treatment; however, the absence of reported recurrences suggests that radical excision may not be necessary.
- Further review of clinical and microscopic features aids in understanding and managing this rare condition.
Abstract:
Epulis is a rare tumor of the newborn, also known as granular cell tumor of the newborn or Neumann's tumor. This tumor arises from the mucosa of the gingiva, most commonly from the anterior part of the maxillary alveolar ridge, and is typically seen as a mass protruding out of the newborn child's mouth, which may interfere with respiration or feeding. Epulis is seen only in the newborn and is a different entity from other granular cell tumors. The tumor has a marked female preponderance of 8:1. The recommended treatment is prompt surgical resection. Recurrences of the tumor and damage to future dentition have not been reported, suggesting that radical excision is not warranted. A newborn female with such a mass is described. The tumor was resected using a carbon dioxide laser; the postoperative course was uneventful. On histologic examination, it was composed of diffuse sheets and clusters of polygonal cells containing small round to oval nuclei and abundant coarsely granular cytoplasm. The tumor cells stained positive for vimentin, and negative for S100-protein, actin, desmin, laminin, keratin, estrogen, and progesterone receptors. Electron microscopic examination showed granular cells containing heterogeneous electron-dense granules, lysosomes, and cytoplasmic lipid droplets. The clinical and microscopic features of such tumors are reviewed.
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