Current Issue January 2012, Vol. 7, No. 1

Issue Highlights

Case reports

Pott's puffy tumor in a 5-year-old boy: The role of ultrasound and contrast-enhanced CT imaging—Surgical case report
January 2012(Vol. 7 | No. 1 | Pages 1-5)
O.M. Vanderveken, K. De Smet, S. Dogan-Duyar, J. Desimpelaere, E.L.I.M. Duval, M. De Praeter, D. Van Rompaey

Mucoepidermoid carcinoma of the tongue in a child
January 2012(Vol. 7 | No. 1 | Pages 6-8)
Mosaad Abdel-Aziz

Penetrating nasal injury with a coat hanger
January 2012(Vol. 7 | No. 1 | Pages 9-11)
David R. Reinstadler, Jonathan B. Salinas, Ali M. Strocker

Cystic fibrosis presenting as bilateral maxillary mucoceles in an infant
01 February 2012
Lana Wazqar, Alipasha Rassouli, Nader Emami Esfahani, Lucia Carpineta, Sam J. Daniel
Abstract: A six months old male presented to our Otolaryngology Department with a long -standing history of chronic nasal congestion and difficulty of breathing. The child was initially treated with n...
Nasal dermal sinus cysts with intracranial extension in a child mosaic for a supernumerary ring chromosome 20
27 January 2012
Bernarda Lozić, Draško Cikojević, Vlatko Ledenko, Marisa Klančnik, Ružica Lasan, Tatijana Zemunik
Abstract: Nasal dermal sinus cysts are congenital malformations that result from anomalous embryological development and are not prescribed to any specific genetic defect. The occurrence of a supernum...
Subglottic stenosis in juvenile rheumatoid arthritis
19 January 2012
Chafeek Tomeh, Nicholas Jones, Parker Velargo, Jerome Thompson
Abstract: Juvenile rheumatoid arthritis (JRA), now termed juvenile idiopathic arthritis (JIA), is a well-described group of arthritides in the pediatric population with known associations with airway ...
Esophageal squamous cell carcinoma in children: A case presentation and review of an unusual entity
09 January 2012
Nilda Süslü, Rezarta Taga Senirli, A. Şefik Hoşal, Burce Özgen Mocan, Mustafa Cengiz
Abstract: Squamous cell carcinoma (SCC) of the esophagus usually occurs between the 4th and 6th decades of life. Esophageal SCC in children is an extremely rare entity – only a few pediatric and adole...
Postextubation stridor in a child with asymptomatic trifid epiglottis with polydactyly – A rare case report
06 January 2012
Sameer Sethi, K.S. Vadaje, Ashok K. Gupta
Abstract: Trifid epiglottis is an extremely rare congenital laryngeal anomaly. Trifid anomaly of epiglottis has not been described in literature. In the embryo, epiglottis, hypothalamus, and digital b...

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On the Cover

New Issue Alert

IJPORL Extra is the new online companion to the International Journal of Pediatric Otorhinolaryngology also published by Elsevier.

Publishing Information

International Journal of Pediatric Otorhinolaryngology Extra is published by Elsevier.

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Journal Access

IJPORL Extra is the new online companion to the International Journal of Pediatric Otorhinolaryngology. Full-text articles are available from 2006 to the present. Access to IJPORL Extra is complimentary.

About IJPORL Extra

International Journal of Pediatric Otorhinolaryngology Extra is a new online-only companion to the International Journal of Pediatric Otorhinolaryngology.

International Journal of Pediatric Otorhinolaryngology Extra publishes case reports that have an important educational value but cannot be published in the printed journal due to lack of space. Case reports published in International Journal of Pediatric Otorhinolaryngology Extra are:

• Peer reviewed to the usual high standards of IJPORL
• Fully citable through digital object identifiers (DOI)
• Rapidly available online via ScienceDirect, the world's leading online journal platform.

Please note that as a new journal International Journal of Pediatric Otorhinolaryngology Extra is NOT currently covered by Pubmed/MEDLINE® and does not have an impact factor.

Authors are requested to submit case reports via the online submission system http://ees.elsevier.com/ijporl/. Authors of accepted papers will be informed whether their case report has been accepted for IJPORL, or more usually, for IJPORL Extra.