Indian Journal of Pathology and Microbiology

IMAGES
Year
: 2014  |  Volume : 57  |  Issue : 1  |  Page : 148--149

Expansile congenital soft-tissue mass: A massive presentation


Ingale Ingale1, Samapika Routray2, Supriya M Kheur3,  
1 Department of Dentistry, Yashwant Chavan Memorial Hospital, Pimpri, Pune, Maharashtra, India
2 Departments of Oral Pathology and Microbiology, Institute of Dental Sciences, 'SOA' University, Kalinganagar, Ghatikia, Bhubaneswar, Odisha, India
3 Departments of Oral Pathology and Microbiology, D.Y. Patil Vidyapeeth's Dr. D.Y. Patil Dental College and Hospital, Pimpri, Pune, Maharashtra, India

Correspondence Address:
Samapika Routray
Department of Oral Pathology and Microbiology, Institute of Dental Sciences, «SQ»SOA«SQ» University, Sector-8, Kalinganagar, Ghatikia, Bhubaneswar - 751 030, Odisha
India




How to cite this article:
Ingale I, Routray S, Kheur SM. Expansile congenital soft-tissue mass: A massive presentation.Indian J Pathol Microbiol 2014;57:148-149


How to cite this URL:
Ingale I, Routray S, Kheur SM. Expansile congenital soft-tissue mass: A massive presentation. Indian J Pathol Microbiol [serial online] 2014 [cited 2021 Sep 23 ];57:148-149
Available from: https://www.ijpmonline.org/text.asp?2014/57/1/148/130931


Full Text

A healthy 5-month-old female child was reported to the out-patient department of our institution with a swelling in the upper lip region which measured about 10 cm × 10 cm in size. Patient's parents gave a history of a small growth of about 1 cm × 1 cm present in the same region at birth and there was gradual increase in size. Clinical examination revealed a growth appearing to arise from palatal tissue, which was firm in nature with no tenderness or palpitations [Figure 1]. All vital signs and investigations were found to be normal. Non-contrast computed tomography scan was carried out, which gave an impression of hypodense mass seen arising from bony palate with fatty component and tiny speck of calcifications within suggestive of dermoid cyst or teratoma [Figure 2]. For further confirmation excisional biopsy of the whole mass was performed. The palatal mass was removed successfully under general anesthesia [Figure 3]. Histopathological examination confirmed it to be teratoma as typical components like immature neural glial tissue was also identified in the tissue mass [Figure 4]. Patient's recovery was fine and there was no recurrence reported until 3 months follow-up.{Figure 1}{Figure 2}{Figure 3}{Figure 4}

Teratomas have a reported incidence of 1:4000 live births with around 2-9% in head and neck sites and congenital teratomas of the oropharyngeal region are usually described as epignathus. 1],[2] We hereby describe a massive expansile mass of congenital origin from the anterior hard palate in a female neonate, diagnosed histopathologically as oral teratoma that was successfully treated with surgery. The etiology of oral teratoma varies, it can be a derivative of the totipotential cells sequestered during embryogenesis or the germ cells giving rise to teratomas by parthenogenetic development. [3] Finally, it may also originate from incomplete formation of Siamese twins also. The differential diagnosis is limited, but includes hamartoma, dermoid cyst and heterotopic gastrointestinal cyst.­[4] As large teratomas in the head and neck are associated with obstruction of airway and difficulty in intubation, mortality rate are generally high in the absence of a well-prepared resuscitation team or meticulous delivery planning to secure the airway. In our case the tumor was attached to the premaxilla with an extending stalk and was removed with no tissue destruction. Later the histopathology evaluation showed typical components like immature neural glial along with disorganized mixture of adipose tissue, mucin secreting glands, etc., confirming it to be an oral teratoma [Figure 4]. As the histopathological diagnosis was confirmatory to rule out all other differential diagnosis no further special immunohistochemical analysis was required. Recurrence was not seen after a 3 months follow-up.

References

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