Bilateral branchial cleft anomaly type two and type three seen together
نویسندگان
چکیده
منابع مشابه
First branchial cleft anomaly.
A 15-year-old girl presented with a cystic swelling since birth behind the ramus of the right mandible and diagnosed clinically as a dermoid cyst. Surgical exploration, however, showed that it was closely related to the external auditory canal, with an extension running medially behind the parotid gland and ending in the bony middle ear. The facial nerve was closely related to the deep part of ...
متن کاملBilateral branchial cleft fistula.
1. Department of Radiology, Kennemer Gasthuis, Haarlem, The Netherlands, 2. Department of Radiology, Academic Medical Center, Amsterdam, The Netherlands Background: An 8-year-old boy was admitted to the pediatric department with two small lumps a few centimeters above the clavicles, medial from the mid-clavicular line, in a symmetrical arrangement (Fig. 1). Sometimes fluid was leaking out of th...
متن کاملOropharyngeal trauma mimicking a first branchial cleft anomaly.
We present a unique and challenging case of a remnant foreign body that presented to us in a child disguised as a strongly suspected congenital branchial cleft anomaly. This case entailed oropharyngeal trauma, with a delayed presentation as a retroauricular cyst accompanied by otorrhea that mimicked the classic presentation of an infected first branchial cleft anomaly. During surgical excision ...
متن کاملA Type-II First Branchial Cleft Anomaly Presenting as a Post-Auricular Salivary Fistula: A Rare Presentation
First branchial cleft anomalies are rare with the average age of presentation as 19 years. There is an average delay of 3.5 years between initial presentation and adequate treatment due to diagnostic dilemma. A very rare variant of first branchial cleft anomaly presenting as a post-auricular salivary fistula is reported. A 12-year-old girl presented with a history of intermittent watery dischar...
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ژورنال
عنوان ژورنال: Journal of Clinical and Experimental Investigations
سال: 2012
ISSN: 1309-6621
DOI: 10.5799/ahinjs.01.2012.01.0120