Collaural fistula

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Collaural fistula
Other namesCervico-aural fistula

Collaural fistula or cervico-aural fistula is a type of fistula whose openings are at external auditory canal and the neck, usually in the upper part of anterior border of sternocleidomastoid muscle. It occurs at birth because the defect is in the embryological branchial cleft. It is rare, and accounts for 8% of the branchial cleft anomalies, which is why it is sometimes misdiagnosed. [1] [2]

Contents

Diagnosis

The patient presents with non-healing ulcers of the neck and one of the external auditory canals. Diagnosis is confirmed by injecting methylene blue dye into the neck opening, and dye coming out of the opening in the external auditory canal. Computerized tomography fistulogram can yield more accurate results regarding the course of the fistula. [3]

Treatment

Treatment of collaural fistula is done by surgical exploration and excision. The fistulous track is removed with skin and cartilage. Split thickness skin grafting and stenting is done if more than 30% of the external canal's circumference has been removed. The potential complications following fistula removal surgery are facial nerve paralysis and recurrence. [2]

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Nasopharyngeal cyst refers to cystic swelling arising from midline and lateral wall of the nasopharynx. The commonest cyst arising from lateral wall is the nasopharyngeal branchial cyst, whereas the mucus retention cysts are the commonest to arise from the midline. Sometimes nasopharyngeal cyst may directly refer to Tornwaldt cyst. It arises from the midline and lies deep to the pharyngobasilar fascia which helps to distinguish it from a mucous retention cyst. The main difference lies in that nasopharyngeal branchial cyst is congenital whereas the Tornwaldt's cyst is acquired.

<span class="mw-page-title-main">Vesicouterine fistula</span> Abnormal communication between the bladder and uterus

Vesicouterine fistula refers to an abnormal communication between the bladder and uterus. The first case of vesicouterine fistula was reported in 1908. It was however first described in 1957 by Abdel Fattah Youssef, an obstetrician and gynaecologist in Kasr el-Aini hospital, Cairo, Egypt. It is characterized by a vesicouterine fistula above the level of the internal os, absence of menstrual bleeding, cyclical presence of blood in urine and absence of urinary incontinence with a patent cervical canal following a lower segment caesarean section. Six of such cases had been reported by other clinicians before the term Menouria was coined by Youssef.

References

  1. Parida, Pradipta Kumar; Alexander, Arun; Raja, Kalairasi; Surianarayanan, Gopalakrishnan; Ganeshan, Sivaraman (2013). "First Branchial Cleft Malformation with Duplication of External Auditory Canal". Case Reports in Otolaryngology. 2013: 578091. doi: 10.1155/2013/578091 . ISSN   2090-6765. PMC   3838813 . PMID   24312740.
  2. 1 2 Pal, Kalyan; Chakraborty, Dipanjan; Kundu, Sohag; Mukhopadhyay, Subrata (18 December 2016). "Collaural Fistula: A Case Report". Bengal Journal of Otolaryngology and Head Neck Surgery. 24 (3): 157–160. doi: 10.47210/bjohns.2016.v24i3.98 . ISSN   2395-2407 . Retrieved 11 May 2018.
  3. Prasad, Sampath Chandra; Azeez, Arun; Thada, Nikhil Dinaker; Rao, Pallavi; Bacciu, Andrea; Prasad, Kishore Chandra (2014). "Branchial Anomalies: Diagnosis and Management". International Journal of Otolaryngology. 2014: 237015. doi: 10.1155/2014/237015 . ISSN   1687-9201. PMC   3960728 . PMID   24772172.