scholarly journals Ectopic parotid tissue with congenital unilateral agenesis of the parotid gland: a rare case presenting with recurrent unilateral cheek swelling

2020 ◽  
Vol 6 (1) ◽  
pp. 10
Author(s):  
D. A. Herath ◽  
U. Kodithuwakku
2014 ◽  
Vol 45 (2) ◽  
pp. 156-160 ◽  
Author(s):  
Gad Murenzi ◽  
Rachel Kaye ◽  
Adam Cole ◽  
Antonio Cajigas ◽  
Samer Khader ◽  
...  
Keyword(s):  

2010 ◽  
Vol 2 (1) ◽  
pp. 6
Author(s):  
Hassan Mohamed Al Bisher

Coexistence of parotid tuberculosis along with a benign parotid tumor is a rare entity with only nine cases reported in the literature. We report here a case of primary parotid tuberculosis with concurrent pleomorphic adenoma in a 51-year-old female.


2015 ◽  
Vol 5 (3) ◽  
pp. 184-187
Author(s):  
Pratik Dipak Shah ◽  
Srijon Mukherji

ABSTRACT Basal cell adenoma (BCA) is a significantly rare benign salivary gland neoplasm that includes isomorphic basaloid cells. Presence of myoepithelial cell is a characteristic of this tumor. Basal cell adenoma accounts for only 1 to 2% of all salivary gland epithelial tumors. The goal of the paper is to report a rare case of tubular type of BCA arising from parotid gland and discuss its management. How to cite this article Shah PD, Mukherji S. Tubular Type of Basal Cell Adenoma of Parotid Gland: A Rare Entity. J Contemp Dent 2015;5(3):184-187.


2007 ◽  
Vol 56 (3) ◽  
pp. 247-249 ◽  
Author(s):  
M. Safioleas ◽  
A. Giannopoulos ◽  
Ch. Manti ◽  
M. Stamatakos ◽  
K. Safioleas ◽  
...  

Author(s):  
Sahil Maingi ◽  
Nishi Sharma ◽  
Ankur Gupta ◽  
Ancy S. Sofia

<p class="abstract">Amyloidoma is a solitary, localized tumor like deposit of amyloid. Amyloidosis can be hereditary or acquired, and it may either be systemic or localized. Amyloidoma of the parotid is a very rare condition, and only a few cases have been described in the literature so far. We report a case of 62 years old male presented with right parotid swelling from last 7 months. Till date only 1 case have been reported so far in the literature. This case has been reported due to rarity of its presentation.</p>


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