Congenital Epulis: A Case and Review of the Literature
نویسندگان
چکیده
منابع مشابه
Congenital epulis of the tongue: A case report and review of the literature
Congenital epulis of the newborn, also known as congenital granular cell tumour, or Neumann’s tumour, is a rare benign tumour. The neoplasm occurs more frequently in the alveolar ridge of the maxilla near the canine than in the mandibular alveolus and has rarely been reported on the tongue. This lesion occurs 10 times more frequently in female infants than male infants suggesting hormonal invol...
متن کاملMultiple Congenital Epulis of the Mandibular Ridge: A Case Report
Congenital epulis is a very rare benign soft-tissue tumor of uncertain histogenesis, which is also known as “gingival granular cell tumor of the newborn”. It occurs almost exclusively as a single tumor along the alveolar ridge of the maxilla in newborn females. Although congenital epulis is strikingly similar to the more common adult granular cell tumor histologically, in contrast to the latter...
متن کاملCongenital epulis of the newborn: report of a case with a review of the Japanese literature.
Congenital granular cell tumor is a rare tumor which arises from alveolus. We describe a case diagnosed and treated in a neonate. Twenty-eight cases have been reported in Japan, with a male:female ratio of 1:6.3. The location of the tumor was the mandible in 13, the maxilla in 15 and multiple in 1. The left side incisor region was the most common site.
متن کاملSpontaneous regression of congenital epulis: a case report and review of the literature
INTRODUCTION Congenital epulis is a rare lesion found on the alveolar process of a newborn child, diagnosed soon after birth. The lesion has a site predilection for the anterior maxillary alveolar process and a 9:1 sex predilection for females. Once diagnosed the traditional management of the lesion has been surgical excision under general anesthesia. CASE PRESENTATION The purpose of this cas...
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ژورنال
عنوان ژورنال: The Bulletin of Tokyo Dental College
سال: 2018
ISSN: 0040-8891
DOI: 10.2209/tdcpublication.2017-0028