Journal of Postgraduate Medicine
 Open access journal indexed with Index Medicus & ISI's SCI  
Users online: 1301  
Home | Subscribe | Feedback | Login 
About Latest Articles Back-Issues Article Submission Resources Sections Etcetera Contact
 
  NAVIGATE Here 
  Search
 
 :: Next article
 :: Previous article 
 :: Table of Contents
  
 RESOURCE Links
 ::  Similar in PUBMED
 ::  Search Pubmed for
 ::  Search in Google Scholar for
 ::Related articles
 ::  Article in PDF (9 KB)
 ::  Citation Manager
 ::  Access Statistics
 ::  Reader Comments
 ::  Email Alert *
 ::  Add to My List *
* Registration required (free) 

  IN THIS Article
 ::  Abstract
 ::  Introduction
 ::  Case report
 ::  Discussion
 ::  References
 ::  Article Figures

 Article Access Statistics
    Viewed5256    
    Printed115    
    Emailed5    
    PDF Downloaded140    
    Comments [Add]    

Recommend this journal


 


 
CASE REPORTS
Year : 1993  |  Volume : 39  |  Issue : 1  |  Page : 36

Congenital epulis.


Dept of Paediatric Surgery, Bai Jerbai Wadia Hospital for Children, Parel, Bombay, Maharashtra.

Correspondence Address:
R Subramaniam
Dept of Paediatric Surgery, Bai Jerbai Wadia Hospital for Children, Parel, Bombay, Maharashtra.

Login to access the Email id

Source of Support: None, Conflict of Interest: None


PMID: 0008295145

Rights and PermissionsRights and Permissions


 :: Abstract 

A tumor was found to be arising from the right maxillary alveolar margin of a newborn baby. No other congenital abnormality was detected. Following excision and histopathological examination, diagnosis of benign congenital granular cell epulis was made. The post-operative course was uneventful.


Keywords: Alveolar Process, Case Report, Female, Granuloma, Giant Cell, congenital,pathology,Human, Infant, Newborn, Maxillary Neoplasms, congenital,pathology,


How to cite this article:
Subramaniam R, Shah R, Kapur V. Congenital epulis. J Postgrad Med 1993;39:36

How to cite this URL:
Subramaniam R, Shah R, Kapur V. Congenital epulis. J Postgrad Med [serial online] 1993 [cited 2019 Nov 21];39:36. Available from: http://www.jpgmonline.com/text.asp?1993/39/1/36/652





  ::   Introduction Top


Congenital epulis is a rare tumour of newborn infant predominantly in girls and is essentially benign. A case history of congenital epulis of the newborn is described. We have also tried to review literature on the same.


  ::   Case report Top


A baby girl weighing 2.8 kg born by normal vertex delivery after an uneventful forty weeks pregnancy was noted to have a large mass arising from the right maxillary alveolar margin. [Figure - 1]

There was no family history of congenital abnormality. Examination findings revealed 5x7x6 cms irregular mass, soft to firm in consistency arising from the maxillary alveolus. Palate and lip were normal. Presence of tumour interfered directly with feeding. There was no evidence of respiratory difficulty. Tumour was excised and the material sent for histopathology. Post- operative recovery was uneventful.

Histopathology showed sheets and nests of large spheroidal and fusiform granular cells showing no aberrant features in a fibrous stroma; covered by squamous epithelium without keratinisation consistent with diagnosis of benign congenital granular cell epulides (GCE).


  ::   Discussion Top


Congenital epulis is strikingly common in females (8F:1M) as also in our case. Maxilla is affected approximately twice as often as the mandible[1].

Five major theories have been put forth to explain the origin and pathology involved i.e. myoblastic, neurogenic, odontogenic, fibrobiastic and histiocytic. However, controversy remains unresolved[2].

Differential diagnosis is granular cell tumor and is made on the basis of (a) female sex preponderance, (b) anterior maxillary location, (c) presence at birth, (d) lack of a pseudoepitheliomatous hyperplasia of overlying squamous epithelium in the latter disorder, and (e) S-100 protein is present in granular cell tumour (GCT) but absent in GCE.

Therefore GCE and GCT have different cells of 2 origin. GCE has most probably a mesenchymal origin.

Another theory is that it is produced due to an intra-uterine stimulus from fetal ovaries, thus explaining the increased female preponderance. It is also known to regress spontaneously[3]. However, limited excision is the treatment of choice. The prognosis is excellent with very rare recurrence[3].

 
 :: References Top

1. Rainey JB, Smith IJ. Congenital epulis of the newborn. J Pediatr Surg 1984; 19:305-306  Back to cited text no. 1    
2.Lifshitz MS, Flotte TJ, Greco MA. Congenital granular cell epulis. Cancer 1984; 53:1845-1848.  Back to cited text no. 2    
3.Cussen LJ, MacMohan RA. Congenital granular cell myobiastoma J Pediatr Surg 1975; 10:249-253.   Back to cited text no. 3    


    Figures

[Figure - 1]



 

Top
Print this article  Email this article
Previous article Next article
Online since 12th February '04
2004 - Journal of Postgraduate Medicine
Official Publication of the Staff Society of the Seth GS Medical College and KEM Hospital, Mumbai, India
Published by Wolters Kluwer - Medknow