Literature DB >> 19566977

A rare variant of first branchial cleft fistula.

S Ramnani1, V Mungutwar, N K Goyal, A Bansal.   

Abstract

OBJECTIVE: We report an extremely rare variant of first branchial cleft anomaly. CASE REPORT: A 15-year-old girl presented with a history of recurrent mucopurulent discharge from an opening in the left infra-auricular region, since birth. Computed tomography fistulography showed a tortuous tract measuring approximately 4.61 cm, extending anteroinferiorly and medially from the external inframeatal opening to the lateral nasopharyngeal wall (anterior to the fossa of Rosenmuller). The tract was connected to the deep lobe of the parotid gland and lay 0.67 cm anterior to the carotid artery and posterior to the medial pterygoid muscle.
CONCLUSION: This was an extremely rare variant of first branchial cleft fistula. To the best of our knowledge, this is the first case of its type to be reported. Computed tomography fistulography is the imaging modality of choice for the diagnosis of branchial cleft fistula, and will also assist surgical planning.

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Year:  2009        PMID: 19566977     DOI: 10.1017/S0022215109990387

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  2 in total

1.  An extremely rare case of adult with first branchial cleft fistula: Case report.

Authors:  Wilfrid Lendoye
Journal:  Ann Med Surg (Lond)       Date:  2021-09-11

2.  A Type-II First Branchial Cleft Anomaly Presenting as a Post-Auricular Salivary Fistula: A Rare Presentation.

Authors:  S Jain; Pt Deshmukh; M Gupta; S Shukla
Journal:  Ann Med Health Sci Res       Date:  2014-01
  2 in total

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