Multiple Congenital Granular Cell Epulis: Case Report and Immunohistochemical Profile with Emphasis on Vascularization

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Multiple Congenital Granular Cell Epulis: Case Report and Immunohistochemical Profile with Emphasis on Vascularization

Congenital granular cell epulis is a rare benign soft tissue lesion arising from the alveolar ridge in neonates. A rare case of multiple congenital granular cell epulis is reported, alongside a description of its vascular immunohistochemical profile. A female newborn presented with two exophytic pedunculated red nodules located on the alveolar ridge between the future eruption sites of the inci...

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Neumann’s Tumour/Congenital Granular Cell Tumour (CGCT)/Granular Cell Epulis Of Infancy is a rare lesion of newborn. It is benign in nature, arising from the alveolar ridge of the gingiva. It is seen more frequently in female neonates. It may cause respiratory and feeding problems.Herewith, we present a case report of CGCT arising from the upper gingival margin of female neonate, treated with s...

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Multiple 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...

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Multiple congenital granular cell epulis in a female newborn: a case report

INTRODUCTION Congenital granular cell epulis is an uncommon tumor which is apparent at birth. CASE PRESENTATION Here we report an unusual case of congenital granular cell epulis present in the mouth of a 4-day-old Asian Chinese female newborn. She had six round, soft, multiple, pedunculated swelling masses, of which two were on her upper anterior ridge and four on her lower anterior ridge. Th...

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ژورنال

عنوان ژورنال: Case Reports in Dentistry

سال: 2015

ISSN: 2090-6447,2090-6455

DOI: 10.1155/2015/878192