Congenital salivary fistula of an accessory parotid gland in Goldenhar syndrome

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.

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.


2008 ◽  
Vol 122 (3) ◽  
Author(s):  
A Gadodia ◽  
A Seith ◽  
R Sharma ◽  
A Thakar

AbstractWe report the imaging findings in a rare case of an accessory parotid gland fistula.Material and methods:An eight-year-old boy was presented with complaints of serous discharge from his left cheek since birth. As part of the radiological investigation, magnetic resonance imaging, computed tomography sialography with fistulography, and digital sialography with fistulography were performed.Results:Magnetic resonance imaging demonstrated the exact location of an accessory parotid gland but failed to demonstrate the accessory duct. The presence of an accessory gland was well delineated on computed tomography fistulography and computed tomography sialography. Fistulography revealed a small accessory parotid duct and gland. No communication between the ductal systems of both glands was demonstrated.Conclusions:In such cases, pre-operative imaging (with sialography, magnetic resonance sialography and computed tomography sialography with fistulography) is helpful for exact delineation of the ductal anatomy. To the best of our knowledge, only four previous cases of congenital accessory parotid gland fistula have been reported in the English literature.


2004 ◽  
Vol 97 (3) ◽  
pp. 245-249 ◽  
Author(s):  
Tatsuhisa Hasegawa ◽  
Masaya Uchida ◽  
Tatsuya Matsunami

2020 ◽  
Vol 36 (1) ◽  
Author(s):  
Dhaifallah Aljeaid ◽  
Ali Mubarak ◽  
Yasser Imarli ◽  
Ohoud Alotaibi

Abstract Background Pneumoparotid is a rare cause of parotid gland swelling. It is due to reflux of air through Stensen’s duct into the parenchyma of the parotid gland. Case presentation A case of self-induced pneumoparotid in a 12-year-old boy is reported. The diagnosis was primarily considered after careful history taking with special attention on the patient’s habits, and it was confirmed by computed tomography. Conclusion Pneumoparotid is a rare but well-documented clinical entity. It should be included in the differential diagnosis of parotid gland swelling.


2015 ◽  
Vol 23 (3) ◽  
pp. 134-138
Author(s):  
Indranil Pal ◽  
Saumitra Kumar ◽  
Anindita Sinhababu ◽  
Kushal Chatterjee

Introduction:Sialectasis of parotid duct is an uncommon condition characterised by abnormal dilatation of a part or whole of the Stensen's duct. It may lead to recurrent parotid infections as well as a cause of concern for the patient. Superficial parotidectomy is the accepted surgical treatment for this condition. Case Report: A case of idiopathic dilatation of parotid duct is presented. It was treated by marsupialisation of the sialectatic segment.This procedure proved to be much simpler and safer than superficial parotidectomy whilst being equally effective. Conclusion: In cases of Stensen's duct sialectasis without any abnormality of the parotid gland, marsupialisation of the ectatic segment should be the treatment of choice.


1965 ◽  
Vol 81 (2) ◽  
pp. 194-198 ◽  
Author(s):  
J. J. CONLEY ◽  
R. M. OLESEN ◽  
R. M. RANKOW ◽  
A. J. SCHWARTZ ◽  
W. A. WEY

1992 ◽  
Vol 106 (2) ◽  
pp. 178-179 ◽  
Author(s):  
J. J. Curtin ◽  
N. T. F. Ridley ◽  
V. L. Cumberworth ◽  
G. W. Glover

AbstractPneumoparotitis is a rare cause of parotid enlargement. It is due to a reflux of air through Stensen's duct into the acini of the parotid gland with subsequent dilatation. We report a case which followed a long history of autoinflation of the middle ears by the Valsalva manoeuvre. The plain radiographic, sialographic and ultrasound findings are presented.


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