Case report of a unilateral cervical chondrocutaneous branchial remnant

Case report of a unilateral cervical chondrocutaneous branchial remnant

International Journal of Pediatric Otorhinolaryngology (2007) 71, 1933—1936 www.elsevier.com/locate/ijporl ABSTRACTS IJPORL Extra Abstracts IJPORL ...

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International Journal of Pediatric Otorhinolaryngology (2007) 71, 1933—1936

www.elsevier.com/locate/ijporl

ABSTRACTS

IJPORL Extra Abstracts IJPORL Extra is the online companion publication to the International Journal of Pediatric Otorhinolaryngology. IJPORL Extra publishes case reports which have an important educational value but cannot be published in the printed journal due to lack of space. Case reports published in the Extra will be peer reviewed in the usual way and can be cited through digital object identifiers (DOI), as can articles published in the printed edition of the regular Journal. These DOIs are published at the foot of each article. Some abstracting and indexing services, such as Medline, do not currently include such publications in their database. For this reason we have decided to include the abstracts of articles published in Extra in the printed edition of the journal. IJPORL Extra is available at http://www. sciencedirect.com/science/journal/18714048 on a complementary basis for entitled institutions subscribing electronically to the regular journal, and on an article pay-per-view basis for others. DOI: 10.1016/S0165-5876(07)00493-4

ABSTRACTS Oropharyngeal second branchial cleft cyst T.S. Anand *, Shashidhar Tatavarty, Swatilika Pal, Ekta Chhabra, Saumitra Kumar Lady Hardinge Medical College (LHMC), ENT, Panchkuyan Road, Connaught Place, 110001 New Delhi, Delhi, India Second arch branchial cleft cysts although a frequently occurring branchial anomaly is almost always located in neck. Its presence in oropharynx 0165-5876/$ — see front matter.

is extremely rare. We report a rare case of second branchial cleft cyst measuring 1 cm  1.1 cm in oropharynx which presented with nasal obstruction and difficulty in swallowing. This cyst was excised and biopsy revealed squamous lined epithelial wall with lymphoid aggregation which is characteristic finding of branchial cleft cyst. Six months follow up of the child was uneventful and there was no recurrence. A review of theories for genesis of branchial cleft cysts is also done. DOI: 10.1016/j.ijporl.2007.06.027

Case report of a unilateral cervical chondrocutaneous branchial remnant Tjouwke A. van Kalkeren a,*, Annelies Frima-van Aarem a, Els J.M. Ahsmann b, Hans F. Mahieu a a Department of Otorhinolaryngology and Head and Neck Surgery, Meander Medical Centre, Amersfoort, The Netherlands b Department of Pathology, Meander Medical Centre, Amersfoort, The Netherlands

Cervical chondrocutaneous branchial remnants are rare and unusual choristomas (dysgenetic tumor, originating from dislocated tissue). To get proper understanding of the etiology and consequently histology, knowledge of early embryologic processes from cartilage structures in the head and neck region is mandatory. A case of a 3 days old girl with a unilateral, cervical chondrocutaneous branchial remnant tumor in the lower half of the neck is presented. DOI: 10.1016/j.ijporl.2007.06.028