Branchial Sinus of the Piriform Fossa: Reappraisal of Third and Fourth Branchial Anomalies

2007 ◽  
Vol 117 (11) ◽  
pp. 1920-1924 ◽  
Author(s):  
Adrian James ◽  
Craig Stewart ◽  
Paul Warrick ◽  
Constance Tzifa ◽  
Vito Forte
2014 ◽  
Vol 5 (2) ◽  
pp. 57-60
Author(s):  
Sagaya Raj ◽  
Azeem Mohiyuddin ◽  
Kouser Mohammadi ◽  
Shuaib Merchant ◽  
Ravindra P Deo ◽  
...  

ABSTRACT Introduction To propose an operation similar to selective neck dissection (levels II, III and IV) as a method of successful management of second arch branchial anomalies. Materials and methods We did a prospective study on patients with branchial arch anomalies from the years 2009 to 2013. They underwent minimal radiological workup. All of them underwent a novel surgical procedure similar to selective neck dissection (levels II, III, IV) that lead to excision of the tract. Patients were followed up for an average period of 2 years. Results We had seven patients which included two branchial sinus, three cysts and two fistulae. All of them were operated and the tract was identified and completely excised by the above approach. None of them had any complications or recurrence on follow-up. Conclusion Branchial arch anomalies are rare congenital problems posing a significant challenge to an ENT surgeon. Inadequate and inappropriate surgeries resulting in recurrences are quite common. Attempts to get either a sinogram or fistulogram are often a failure and cumbersome. Selective neck dissection from levels II to IV is a surgical maneuver which allows access to the involved anatomical segment of the neck. Thus, it is a structured and methodical approach that comprehensively leads to excision of the complete tract. It also reduces the chances of complications. Recurrences are rare with this technique. How to cite this article Merchant S, Mohiyuddin A, Deo RP, Raj S, Nawaz S, Mohammadi K. Selective Neck Dissection: A Novel Technique for Second Branchial Arch Anomalies. Int J Head Neck Surg 2014;5(2):57-60.


2021 ◽  
Vol 9 ◽  
pp. 2050313X2110145
Author(s):  
Dorji Penjor ◽  
Morimasa Kitamura

Collaural fistula is a very rare Work Type II first branchial cleft anomaly in which there is a complete fistulous tract between external auditory canal and the neck. Misdiagnosis and mismanagement can lead to prolonged morbidity and complications due to repeated infections. We present a case of an 18-year-old lady with a recurrent discharging sinus on her neck for 4 years. She has been treated with repeated incision and drainage and multiple antibiotics in the past. Otoscopic examination revealed an opening on the floor of the left external auditory canal. A diagnosis of an infected collaural fistula was made. Complete excision of the fistulous tract was done after treatment of the active infection. On follow-up, there was no further recurrence at 1 year. Sound knowledge of embryology of branchial anomalies with good history and examination is important to make correct and early diagnosis to prevent morbidity.


2000 ◽  
Vol 56 (3) ◽  
pp. 244-245
Author(s):  
KL SAMPATH KUMAR
Keyword(s):  

2021 ◽  
Vol 14 (3) ◽  
pp. e241081
Author(s):  
Sevasti Konstantinidou ◽  
Michelle Wyatt ◽  
Colin Butler ◽  
Claire Frauenfelder

A bilobed tongue base was identified in an infant with multiple other head, neck and cardiac congenital anomalies. This anatomical variation of the posterior tongue is rare, with only two other cases identified in the literature. We report a case of a 5-month-old boy with a bilobed posterior tongue incidentally identified during workup for cardiac surgery.


2021 ◽  
Vol 8 (11) ◽  
pp. 375-377
Author(s):  
Ashoka Nand Thakur ◽  
Priyambada .

Branchial cleft anomalies are well described, with the second arch anomaly being the commonest. Remains of cervical sinus of His may persist as a branchial cyst. A branchial sinus is formed when 2nd branchial arch fails to meet the 5th pharyngeal arch. Peak age for presentation of branchial cysts is in the third decade and that of the congenital sinuses and fistulae is at birth. The association of a branchial cyst with branchial sinus is very rare. We are presenting two cases had branchial cyst along with branchial sinus. It was managed successfully with complete excision. Histopathological examination confirmed the association. Keywords: Branchial Sinus, Branchial cyst,


2019 ◽  
Vol 54 (8) ◽  
pp. 1702-1707 ◽  
Author(s):  
Marie-Eva Rossi ◽  
Eric Moreddu ◽  
Nicolas Leboulanger ◽  
Mohamed Akkari ◽  
Jean-Michel Triglia ◽  
...  

1997 ◽  
Vol 123 (4) ◽  
pp. 438-441 ◽  
Author(s):  
J. L. Edmonds ◽  
D. A. Girod ◽  
J. M. Woodroof ◽  
D. E. Bruegger
Keyword(s):  

2005 ◽  
Vol 114 (7) ◽  
pp. 529-532 ◽  
Author(s):  
Christopher Y. Chang ◽  
Julia A. Furdyna

A case report of bilateral pharyngoceles without a history of elevated intrapharyngeal pressures is used to support the hypothesis that pharyngoceles may be an adult manifestation of an internal branchial sinus anomaly. The development of a pharyngocele from a branchial sinus origin would suggest a predictable relationship to the hypoglossal, glossopharyngeal, and superior laryngeal nerves, which may influence the choice of surgical approach (open versus endoscopic) and the counseling of patients who are considering surgical correction.


1990 ◽  
Vol 20 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Jeffrey I. Feldman ◽  
Donald B. Kearns ◽  
Seth M. Pransky ◽  
Allan B. Seid
Keyword(s):  

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