scholarly journals Accessory Parotid Gland Tumor and Tumor Arising from Stensen's Duct

2004 ◽  
Vol 97 (3) ◽  
pp. 245-249 ◽  
Author(s):  
Tatsuhisa Hasegawa ◽  
Masaya Uchida ◽  
Tatsuya Matsunami
1997 ◽  
Vol 24 (1) ◽  
pp. 105-110 ◽  
Author(s):  
Arata Horii ◽  
Yuichiro Honjo ◽  
Michihiro Nose ◽  
Masayoshi Ozaki ◽  
Jun-Ichi Yoshida

2021 ◽  
pp. 014556132110362
Author(s):  
Rohith S. Voora ◽  
Joshua Stramiello ◽  
Emily Funk ◽  
Joseph Califano

Accessory parotid gland (APG) tumors account for 1% to 7% of all parotid gland neoplasms but are more likely to be malignant than main parotid gland tumors. Management of APG neoplasms entails surgical excision. Four primary approaches to resection have been described in the literature with varying facial nerve outcomes. We report a case of a 4-cm APG pleomorphic adenoma utilizing a transoral approach for excision without postoperative facial nerve injury. A transoral approach is known to mitigate patients’ cosmetic concerns; however, prior reports utilized endoscopic assistance on patients with smaller tumors. We conclude that large APG tumors can be excised through a transoral approach without undue risk to the distal facial nerves, though this transoral approach ultimately may not be appropriate for malignant neoplasms or difficult dissections.


2017 ◽  
Vol 110 (11) ◽  
pp. 739-742
Author(s):  
Kunihiko Tokashiki ◽  
Shigetaka Shimizu ◽  
Kiyoaki Tsukahara

1996 ◽  
Vol 89 (7) ◽  
pp. 839-844
Author(s):  
Hiromitsu Saito ◽  
Hiroyuki FUJITA ◽  
Tomoyuki YOSHIDA ◽  
Fumihisa HIRAIDE

2011 ◽  
Vol 126 (1) ◽  
pp. 103-107 ◽  
Author(s):  
Z Sun ◽  
L Sun ◽  
Z Zhang ◽  
X Ma

AbstractObjectives:We report two cases of congenital salivary fistula of an accessory parotid gland, and we discuss its occurrence in Goldenhar syndrome.Methods:Two teenagers complained of a congenital cheek fistula with constant salivary discharge. Computed tomography fistulography and sialography were performed. The diagnosis of Goldenhar syndrome was established based on clinical and imaging findings. Previously reported cases are reviewed and the clinical and radiological features summarised.Results:In these two patients, a salivary fistula of an accessory parotid gland was demonstrated on computed tomography fistulography, and did not communicate with Stensen's duct. Deformity of Stensen's duct and hypoplasia of the ipsilateral mandibular ramus were present. Tragal appendices have frequently been reported in such cases.Conclusion:A congenital cheek salivary fistula of an accessory parotid gland should be considered indicative of Goldenhar syndrome.


2018 ◽  
Vol 152 (0) ◽  
pp. 54-54
Author(s):  
Kunihiko Tokashiki ◽  
Shigetaka Shimizu ◽  
Kiyoaki Tsukahara

2002 ◽  
Vol 116 (4) ◽  
pp. 312-313 ◽  
Author(s):  
Dong-Hee Lee

We report a case of an abscess from an ’ectopic’ accessory parotid gland in the cheek demonstrated by sialography and computed tomography (CT). The accessory parotid gland was ectopically located anterolateral to the masseter muscle and isolated from the main parotid gland. The orifice and ductal system of the ectopic accessory parotid gland were separated from those of Stensen’s duct. The abscess developed from this ectopic accessory gland, and the main parotid gland was free of inflammation. Using sialography and CT, we confirmed the presence of this ectopic accessory gland.


2015 ◽  
Vol 20 (1) ◽  
pp. 43-45
Author(s):  
Kazi Atikuzzaman

The accessory parotid gland is salivary tissue separated from the main parotid gland and lying on masseter muscle. The accessory parotid gland is not rare, according to cadaver studies, but neoplasm in the accessory parotid gland is rare. Surgical excision is the treatment of choice for the accessory parotid gland tumour. It is important to identify the buccal branch of the facial nerve to avoid injury to the facial nerve. Herein we describe a case of accessory parotid gland tumor in a 30 years old lady. Histopathological diagnosis was Warthin’s tumour which is very rare in female. DOI: http://dx.doi.org/10.3329/bjo.v20i1.22017 Bangladesh J Otorhinolaryngol; April 2014; 20(1): 43-45


Sign in / Sign up

Export Citation Format

Share Document