scholarly journals Pleomorphic Adenoma of the Parotid Gland: A Case Report

2021 ◽  
Vol 5 (3) ◽  
pp. CR6-CR9
Author(s):  
Rajesh Gupta ◽  
Preety Gupta ◽  
Shivani Gupta ◽  
Sumit Garg

Salivary organ tumors are uncommon, including under 3 % of all neoplasia of head and neck district. Pleomorphic adenoma is the most well-known salivary organ tumor, representing 60-80% of amiable tumors of salivary organs. Generally they are found as singular one-sided, firm and portable, effortless, moderate developing mass. The board includes careful resection by shallow or absolute parotidectomy.

2017 ◽  
Vol 7 (3) ◽  
pp. 1-5
Author(s):  
Dawid Zagacki ◽  
Kazimierz Niemczyk ◽  
Antoni Bruzgielewicz ◽  
Alina Morawiec-Sztandera ◽  
Marcin Braun ◽  
...  

Salivary gland neoplasms represent about 3% of head and neck tumors. The area most affected by tumors is parotid salivary gland (standing for about 80% of all cases). The most common type of the neoplasm is pleomorphic adenoma (which accounts for 80-90% of all diagnoses). One of the rare diagnoses in this region comprises synovial sarcoma, as it mainly occurs in lower extremities. In head and neck region it accounts for about 3% of all diagnoses. About 20 cases have been described in this region, so far. The etiology of the disease remains unknown, but there are reports linking synovial sarcoma with the rearrangement in the gene responsible for chromosomal transcription t(X;18) (p11,q11).


2021 ◽  
Vol 156 (Supplement_1) ◽  
pp. S86-S87
Author(s):  
M Khazaeli ◽  
Z Kamaluddin ◽  
M Taherian

Abstract Introduction/Objective Myoepithelial carcinoma is identified by nearly exclusive myoepithelial differentiation and evidence of malignancy. It may arise de novo or in preexisting benign tumors including pleomorphic adenoma and benign myoepithelioma. It occurs most commonly in the parotid gland followed by submandibular glands, minor salivary glands, and occasionally in the sublingual gland. Nasopharyngeal origin has been rarely reported. Methods/Case Report An afebrile 19-year-old female presented to the emergency department with persistent facial pressure, otalgia (right side greater than left side), rhinorrhea, and several episodes of epistaxis. One month before, she has been treated with Amoxicillin for three days with no relief, where Augmentin started for her for five days. About four days prior presentation, she was placed on Prednisone and Cefdinir. Over the next several days, she began having throat pain with difficulty swallowing. Routine blood work revealed a leukocytosis of 14.2 with normal differentiation. CT of the neck showed a large soft tissue mass centered at the right nasopharynx. Flexible nasal endoscopy performed bilaterally to reveal the nasopharynx is entirely obstructed with a lobulated mass filling the nasopharynx. On the right side, it extends into the posterior nasal passage filling the sphenoethmoid recess and the posterior floor of the nasal passage. Outpatient biopsy from nasopharynx mass is also performed. Results (if a Case Study enter NA) Mass biopsy reveals a mucinous and chondromyxoid background with mixed epithelial and myoepithelial differentiation. The is squamous metaplasia of myoepithelial cells and prominent mitotic activity and apoptotic activity. Immunohistochemistry was positive for CK5/6, calponin, BCL2, SMA, BerEp4, Sox10, and a proliferative index up to 40%. Based on this information Myoepithelial Carcinoma ex-pleomorphic adenoma of the nasopharynx is the diagnosis. Conclusion Carcinoma ex pleomorphic adenoma is usually a high-grade malignancy. It occurs most commonly in the parotid gland, followed by submandibular glands, minor salivary glands, and occasionally in the sublingual gland. Our case is one of the few cases of myoepithelial carcinoma arising in nasopharyngeal pleomorphic adenoma.


2016 ◽  
Vol 17 (2) ◽  
pp. 111-114 ◽  
Author(s):  
Santosh K. Swain ◽  
Mahesh C. Sahu ◽  
Satyajit Mishra

Author(s):  
R.H. Khonsari ◽  
C. Bertoïa-Caufourier ◽  
G. Murcier ◽  
G. Hervé ◽  
A. Assouline ◽  
...  

2014 ◽  
Vol 14 (1) ◽  
pp. 88-91 ◽  
Author(s):  
Tejinder Kataria ◽  
Shyam S Bisht ◽  
Deepak Gupta ◽  
Ashu Abhishek ◽  
Govardhan Hb ◽  
...  

AbstractMetastases to the parotid region are relatively infrequent and originate primarily from head and neck cancer. Metastases of an infraclavicular origin are uncommon. Moreover, metastasis from the carcinoma of urinary bladder (CUB) to any part of the head and neck, including parotid gland, is rare. Surgery and chemotherapy are usually offered. We report a case of solitary parotid metastasis from CUB, who was successfully treated with stereotactic body radiotherapy (SBRT) using CyberKnife. SBRT is a safe alternative in cases unwilling/unfit for surgery.


Sign in / Sign up

Export Citation Format

Share Document