Congenital Granular Cell Epulis

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منابع مشابه

Congenital Granular Cell Epulis (Neumann’s Tumour): A Rare Case Report

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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Congenital granular cell tumor (congenital epulis): a lesion of multidisciplinary interest.

Congenital granular cell tumor (CGCT), or congenital epulis, is a very uncommon benign soft tissue lesion that usually arises from the alveolar mucosa of neonates and may cause respiratory and feeding problems. We report a case of a 3-day-old female newborn, who presented an intraoral tumor mass which was protruding from her mouth, and compromising feeding. Under general anesthesia, the lesion ...

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Congenital epulis.

Congenital epulis of the newborn is a rare gingival tumor that occurs along the alveolar ridge. We report the prenatal sonographic and postnatal MR imaging findings in an infant with maxillary and mandibular congenital epulides.

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Congenital epulis.

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...

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A case report of a huge congenital granular cell epulis operated under local anesthesia

Congenital granular cell epulis (CGCE) is a very rare benign soft tissue lesion of the neonate, it most frequently located on the anterior maxillary alveolar ridge. It has a female predilection. It is a tumor with no tendency to recur after excision. The exact histogenesis of this tumor remains unresolved and it may be hamartomata.

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ژورنال

عنوان ژورنال: Archives of Pathology & Laboratory Medicine

سال: 2014

ISSN: 1543-2165,0003-9985

DOI: 10.5858/arpa.2012-0306-rs