scholarly journals Pediatric Pleomorphic Adenoma of the Parotid: Case Report, Review of Literature and Novel Therapeutic Targets

Children ◽  
2018 ◽  
Vol 5 (9) ◽  
pp. 127 ◽  
Author(s):  
Girish Gulab Meshram ◽  
Neeraj Kaur ◽  
Kanwaljeet Singh Hura

Salivary gland tumors are extremely rare and encompass a diverse group of histologies. Less than 5% of the affected population is pediatric. We present a case of 6-year-old child with pleomorphic adenoma of the parotid. The patient underwent a superficial parotidectomy. Recurrence was not observed in the six months of follow-up. Surgery is the mainstay of the management of benign salivary gland tumors. Although novel molecular agents are being explored, personalized therapy would be a challenge due to the rarity and vast genetic/histologic variations of salivary gland tumors.

2014 ◽  
Vol 5 (1) ◽  
pp. 25-27
Author(s):  
Sunil Kumar ◽  
Ashwini Sethi ◽  
Satwinder Pal Singh

ABSTRACT Very few cases of oncocytoma parotid have been reported in literature. Because of its rarity (less than 1% of salivary gland tumors) and clinical presentation of the tumor, there is a tendency among the clinicians to misdiagnose it as pleomorphic adenoma, hemangioma or other forms of oncocytosis. Only a histopathological examination can confirm it. We report here a case of oncocytoma of parotid gland in a 70-year-old male who had the tumor for over 9 years. How to cite this article Kumar S, Sethi A, Singh SP, Sharma V. Oncocytoma Parotid Gland: A Case Report and Brief Review of Literature. Int J Head Neck Surg 2014;5(1):25-27.


2019 ◽  
Vol 6 (4) ◽  
pp. 1418
Author(s):  
Jeevan G. Sanjive ◽  
N. S. Reddy ◽  
V. Soundara Rajan

Parotid oncocytoma presents in less than 1% of salivary gland tumors. Therefore, there are only very few reported cases in literature. This tumor is often diagnosed in elderly age group. It is often misdiagnosed clinically as pleomorphic adenoma, hemangioma or Warthin’s tumor. CT imaging usually shows an enhancing lobulated mass; however, it cannot exactly diagnose oncocytoma. It can be confirmed only by histopathological examination. This case report is of an Indian female of 66 years with parotid swelling who underwent total conservative parotidectomy. Post operatively, patient has no residual disease and complications.


2021 ◽  
Vol 14 (9) ◽  
pp. e243319
Author(s):  
Priya K Nair ◽  
Beena R Varma ◽  
Ravi Veeraraghavan ◽  
Mahija Janardhanan

Canalicular adenoma is a unique, rare, benign salivary gland neoplasm whose reported prevalence varies in different studies. According to literature, this neoplasm has a marked predilection to occur in the upper lip of elderly women. Histological features are usually distinctive and diagnostic. This neoplasm has good prognosis after conservative surgical management but the propensity of multifocal nature and recurrence of this lesion mandates regular follow-up. This case report illustrates the case of a canalicular adenoma in the palate in a 71-year-old male patient. Here, we discuss the differential diagnosis with a brief review of literature.


2018 ◽  
Vol 14 (4) ◽  
pp. 225-227
Author(s):  
Radha Baral ◽  
Bidhata Ojha ◽  
Dipshikha Bajracharya ◽  
Sumit Singh

Myoepithelioms are rare benign salivary gland tumors representing 1–1.5% of all salivary gland tumors. It was once considered to be one end of the histologic spectrum of pleomorphic adenoma (PA), but myoepitheliomas today are believed to be distinct entity. Herein we report a case of myoepithelioma in a 49 years old female patient with the history of swelling in the soft and hard palate. The diagnosis was made on the basis of histopathological findings and immunohistochemical report.  


Author(s):  
Costantino Ricci ◽  
Federico Chiarucci ◽  
Francesca Ambrosi ◽  
Tiziana Balbi ◽  
Barbara Corti ◽  
...  

AbstractThe presence of melanin pigment and melanocytic markers expression have been rarely reported in salivary gland tumors. Herein, two cases of carcinoma arising in pleomorphic adenoma of the parotid gland and showing diffuse expression of myoepithelial and melanocytic markers are described. The clinical-pathological clues useful in the differential diagnosis with melanoma are discussed. In addition, a review of the pertinent literature is also proposed, discussing the pathologic mechanisms potentially involved in this phenomenon.


2017 ◽  
Vol 23 (4) ◽  
pp. e9-e13
Author(s):  
S.A. Lalé ◽  
E.B. Burger ◽  
J.H.J.M. Bessems ◽  
V. Pollet ◽  
C.A. van Nieuwenhoven

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