dc.contributor.author |
Bilen, BT |
|
dc.contributor.author |
Alaybeyoglu, N |
|
dc.contributor.author |
Arslan, A |
|
dc.contributor.author |
Turkmen, E |
|
dc.contributor.author |
Asian, S |
|
dc.contributor.author |
Celik, M |
|
dc.date.accessioned |
2022-03-14T08:40:40Z |
|
dc.date.available |
2022-03-14T08:40:40Z |
|
dc.date.issued |
2004 |
|
dc.identifier.uri |
http://hdl.handle.net/11616/55284 |
|
dc.description.abstract |
Congenital gingival granular cell tumours; (CGCT) are rare and always benign intraoral tumours originating from the alveolar ridge. They are also known as congenital epulis, congenital myobtastoma or Neumann's tumour. They are typically seen as a mass protruding out of a newborn child's mouth. In general., CGCT occurs as a solitary tumour. The main differential diagnosis is epignathus (oral teratoma). |
|
dc.description.abstract |
This report describes a newborn with a mass originating from tower alveolar ridge obtruding into the oral cavity. |
|
dc.description.abstract |
Clinical features, histiogenesis and necessity for early surgical treatment due to risk of airway obstruction and difficulty in feeding were discussed. (C) 2004 Elsevier Ireland Ltd. All rights reserved. |
|
dc.source |
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY |
|
dc.title |
Obstructive congenital gingival granular cell tumour |
|