Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report

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...

Full description

Bibliographic Details
Main Authors: Dorji Penjor, Morimasa Kitamura
Format: Article
Language:English
Published: SAGE Publishing 2021-05-01
Series:SAGE Open Medical Case Reports
Online Access:https://doi.org/10.1177/2050313X211014515
id doaj-b7ae76e42dbb4c6e9e78cba14f070032
record_format Article
spelling doaj-b7ae76e42dbb4c6e9e78cba14f0700322021-05-13T22:03:30ZengSAGE PublishingSAGE Open Medical Case Reports2050-313X2021-05-01910.1177/2050313X211014515Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case reportDorji Penjor0Morimasa Kitamura1Department of Otorhinolaryngology, Jigme Dorji Wangchuck National Referral Hospital, Thimphu, BhutanDepartment of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, JapanCollaural 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.https://doi.org/10.1177/2050313X211014515
collection DOAJ
language English
format Article
sources DOAJ
author Dorji Penjor
Morimasa Kitamura
spellingShingle Dorji Penjor
Morimasa Kitamura
Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
SAGE Open Medical Case Reports
author_facet Dorji Penjor
Morimasa Kitamura
author_sort Dorji Penjor
title Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
title_short Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
title_full Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
title_fullStr Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
title_full_unstemmed Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report
title_sort collaural fistula (work type ii first branchial cleft anomaly) with prolonged morbidity: a case report
publisher SAGE Publishing
series SAGE Open Medical Case Reports
issn 2050-313X
publishDate 2021-05-01
description 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.
url https://doi.org/10.1177/2050313X211014515
work_keys_str_mv AT dorjipenjor collauralfistulaworktypeiifirstbranchialcleftanomalywithprolongedmorbidityacasereport
AT morimasakitamura collauralfistulaworktypeiifirstbranchialcleftanomalywithprolongedmorbidityacasereport
_version_ 1721441907326844928