First Branchial Cleft Malformation with Duplication of External Auditory Canal

First branchial cleft anomalies are uncommon, accounting for less than 10% of all branchial abnormalities. Their rare occurrence and varied presentation have frequently led to misdiagnosis and inadequate and inappropriate treatment of these conditions leading to repeated recurrences and secondary in...

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Main Authors: Pradipta Kumar Parida, Arun Alexander, Kalairasi Raja, Gopalakrishnan Surianarayanan, Sivaraman Ganeshan
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Case Reports in Otolaryngology
Online Access:http://dx.doi.org/10.1155/2013/578091
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author Pradipta Kumar Parida
Arun Alexander
Kalairasi Raja
Gopalakrishnan Surianarayanan
Sivaraman Ganeshan
author_facet Pradipta Kumar Parida
Arun Alexander
Kalairasi Raja
Gopalakrishnan Surianarayanan
Sivaraman Ganeshan
author_sort Pradipta Kumar Parida
collection DOAJ
description First branchial cleft anomalies are uncommon, accounting for less than 10% of all branchial abnormalities. Their rare occurrence and varied presentation have frequently led to misdiagnosis and inadequate and inappropriate treatment of these conditions leading to repeated recurrences and secondary infection. In this paper, a case of 11-year girl with type 2 first branchial cleft defect is described. She first presented with a nonhealing ulcer of upper neck from childhood. Diagnosis had previously been missed and treated as tubercular ulcer. We confirmed the correct diagnosis by history and computerized tomography fistulogram. The lesion was completely excised with no further recurrence.
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institution Kabale University
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publishDate 2013-01-01
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series Case Reports in Otolaryngology
spelling doaj-art-2fdab9bf5f8f49d48d13e5ab3ea99d2a2025-02-03T06:11:22ZengWileyCase Reports in Otolaryngology2090-67652090-67732013-01-01201310.1155/2013/578091578091First Branchial Cleft Malformation with Duplication of External Auditory CanalPradipta Kumar Parida0Arun Alexander1Kalairasi Raja2Gopalakrishnan Surianarayanan3Sivaraman Ganeshan4Department of E.N.T, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry 605006, IndiaDepartment of E.N.T, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry 605006, IndiaDepartment of E.N.T, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry 605006, IndiaDepartment of E.N.T, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry 605006, IndiaDepartment of E.N.T, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry 605006, IndiaFirst branchial cleft anomalies are uncommon, accounting for less than 10% of all branchial abnormalities. Their rare occurrence and varied presentation have frequently led to misdiagnosis and inadequate and inappropriate treatment of these conditions leading to repeated recurrences and secondary infection. In this paper, a case of 11-year girl with type 2 first branchial cleft defect is described. She first presented with a nonhealing ulcer of upper neck from childhood. Diagnosis had previously been missed and treated as tubercular ulcer. We confirmed the correct diagnosis by history and computerized tomography fistulogram. The lesion was completely excised with no further recurrence.http://dx.doi.org/10.1155/2013/578091
spellingShingle Pradipta Kumar Parida
Arun Alexander
Kalairasi Raja
Gopalakrishnan Surianarayanan
Sivaraman Ganeshan
First Branchial Cleft Malformation with Duplication of External Auditory Canal
Case Reports in Otolaryngology
title First Branchial Cleft Malformation with Duplication of External Auditory Canal
title_full First Branchial Cleft Malformation with Duplication of External Auditory Canal
title_fullStr First Branchial Cleft Malformation with Duplication of External Auditory Canal
title_full_unstemmed First Branchial Cleft Malformation with Duplication of External Auditory Canal
title_short First Branchial Cleft Malformation with Duplication of External Auditory Canal
title_sort first branchial cleft malformation with duplication of external auditory canal
url http://dx.doi.org/10.1155/2013/578091
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