منابع مشابه
Congenital Epulis: a Case Report
Congenital epulis is a rare lesion of the newborn. A case of congenital epulis is presented here with details on the clinical, histopathological characteristics as well as the management of the lesion.
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. Report of a case.
The clinical characteristics and histogenesis of congenital epulis, the tumour often confused with granular cell myoblastoma, are discussed and a case of our own is presented.
متن کاملCongenital fibrous epulis: a case report.
Intra-oral examination showed a soft fluctant non-haemorrhagic lesion at the left central incisor region of the maxilla arising from the crest of the alveolus (Fig. I). It was a pedunculated, well circumscribed bean-shaped mass of soft tissue measuring approximately 1.5 x 1.0 x 1.5 cm. The clinical diagnosis was congenital epulis. The lesion was excised a week later and the tissue sent for hist...
متن کاملCongenital Epulis: A Case Report and Estimation of Incidence
Congenital Epulis, also known as Neumann's tumour, is a rare congenital growth affecting the gingival mucosa of neonates. It is benign condition, seen more frequently in females, with multiple Epuli occurring in only 10% of cases. The cause and origin of Congenital Epulis remains unclear. In this article we present a case report of an otherwise healthy female neonate with two Congenital Epuli a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Japanese Journal of Oral & Maxillofacial Surgery
سال: 1981
ISSN: 2186-1579,0021-5163
DOI: 10.5794/jjoms.27.1507