International Journal of Pediatric Otorhinolaryngology Extra This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.

Sialoblastoma: A Very Rare Cervical Mass in Neonates: a case report
Sialoblastomas are very rare epithelial tumors of the salivary gland that usually occur in the parotid or submandibular gland. Most sialoblastomas present in the neonatal period or early childhood. The biological behavior of these tumors is variable, with a potential for local and systemic recurrences. Only ten cases in the submandibular gland have been reported so far. We are reporting a case of sialoblastoma in a newborn male child presenting in the right submandibular region. Ultrasound visualized a homogeneous solid mass. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 4, 2016 Category: ENT & OMF Authors: Ala’a Hamdan, Jean-Yves Sichel, Oleg Kharenko, Pierre Attal Tags: Case Report Source Type: research

Myoepithelial carcinoma of the hypopharynx
We present an unusual case arising in a 1-year-old boy. He underwent microsuspension direct laryngoscopy with organ preservation. The tumor cells were arranged in nests and lobules separated by thin fibrovascular septae in a background of fibromyxoid stroma. Immunohistochemically, the tumor was positive for S-100 protein, AE1/AE3, and synaptophysin. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 3, 2016 Category: ENT & OMF Authors: Kazuhira Endo, Hiroshi Yoshida, Yosuke Nakanishi, Akira Tsuji, Satoru Kondo, Naohiro Wakisaka, Shigeyuki Murono, Tomokazu Yoshizaki Tags: Case report Source Type: research

Sialoblastoma: A very rare cervical mass in neonates: A case report
Sialoblastomas are very rare epithelial tumors of the salivary gland that usually occur in the parotid or submandibular gland. Most sialoblastomas present in the neonatal period or early childhood. The biological behavior of these tumors is variable, with a potential for local and systemic recurrences. Only ten cases in the submandibular gland have been reported so far. We are reporting a case of sialoblastoma in a newborn male child presenting in the right submandibular region. Ultrasound visualized a homogeneous solid mass. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 3, 2016 Category: ENT & OMF Authors: Ala ’a Hamdan, Jean-Yves Sichel, Oleg Kharenko, Pierre Attal Tags: Case report Source Type: research

Cochlear implantation in a child with subtelomeric 1q deletion syndrome and Dandy–Walker malformation
We report a 2-year-old boy with subtelomeric 1q deletion syndrome presented with typical craniofacial abnormalities and bilateral senserineural hearing loss. Imaging revealed corpus callosum hypogenesis and Dandy-Walker malformation. Cochlear implantation was successfully undertaken using a transmastoid facial recess aproach. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 2, 2016 Category: ENT & OMF Authors: Raşit Cevizci, Selin Üstün Bezgin, Handan Turan Dizdar, Oğuz Yılmaz, Burak Kersin, Yıldırım A. Bayazıt Tags: Case report Source Type: research

Cochlear implantation in a child with subtelomeric 1q deletion syndrome and Dandy-Walker malformation
Subtelomeric 1q deletion syndrome is a rare disorder, first described by Mankinen et al. in 1976 [1]. Patients with this syndrome are characterized by mental and growth retardation with prenatal onset, microcephaly, seizures, short neck, hand and foot abnormalities, hypospadias and a variety of other midline defects, including corpus callosum, cardiac, genital, and gastro-esophageal abnormalities [2]. The facial features of patients include a full, round face with prominent forehead, upward slanting palpebral fissures, epicanthic folds, a short, broad nose with a flat nasal bridge, thin lips, downturn corners of mouth, mic...
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 2, 2016 Category: ENT & OMF Authors: Raşit Cevizci, Selin Üstün Bezgin, Handan Turan Dizdar, Oğuz Yılmaz, Burak Kersin, Yıldırım A. Bayazıt Tags: Case Report Source Type: research

Cochlear implantation in a child with subtelomeric 1q deletion syndrome and Dandy –Walker malformation
We report a 2-year-old boy with subtelomeric 1q deletion syndrome presented with typical craniofacial abnormalities and bilateral senserineural hearing loss. Imaging revealed corpus callosum hypogenesis and Dandy-Walker malformation. Cochlear implantation was successfully undertaken using a transmastoid facial recess aproach. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - March 1, 2016 Category: ENT & OMF Authors: Ra şit Cevizci, Selin Üstün Bezgin, Handan Turan Dizdar, Oğuz Yılmaz, Burak Kersin, Yıldırım A. Bayazıt Tags: Case report Source Type: research

WITHDRAWN: Lingual leiomyomatous hamartoma with bifid tip of tongue and ankyloglossia in an infant
This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause.The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 20, 2016 Category: ENT & OMF Authors: Anjan Kumar Dhua, Kashish Kumar, Murali Krishna Nagendla, Veereshwar Bhatnagar, Asit Ranjan Mridha Source Type: research

Lingual leiomyomatous hamartoma with bifid tip of tongue and ankyloglossia in an infant
Lingual leiomyomatous hamartoma (LLH) is a rare and underreported entity as a differential diagnosis of midline lingual swellings. LLH with bifid tongue and ankyloglossia is still rarer and so far only one case report in an adult exists in the literature.Here we report a 5 months infant with this rare association. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 20, 2016 Category: ENT & OMF Authors: Anjan Kumar Dhua, Kashish Kumar, Murali Krishna Nagendla, Veereshwar Bhatnagar, Asit Ranjan Mridha Tags: Case Report Source Type: research

WITHDRAWN: Lingual leiomyomatous hamartoma with bifid tip of tongue and ankyloglossia in an infant
This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause.The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 19, 2016 Category: ENT & OMF Authors: Anjan Kumar Dhua, Kashish Kumar, Murali Krishna Nagendla, Veereshwar Bhatnagar, Asit Ranjan Mridha Source Type: research

Management of Airway Obstruction in Two Cases of Head and Neck Teratoma
We present two such cases in this article. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 18, 2016 Category: ENT & OMF Authors: C.L. Zhao, R.C. Anicete, H.K. Tan Tags: Case Report Source Type: research

Management of airway obstruction in two cases of head and neck teratoma
We present two such cases in this article. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 17, 2016 Category: ENT & OMF Authors: C.L. Zhao, R.C. Anicete, H.K. Tan Tags: Case Report Source Type: research

WITHDRAWN: Acute peripheral facial paralysis following varicella infection: an uncommon complication
This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause.The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 10, 2016 Category: ENT & OMF Authors: Damla Hanalioglu, Yasemin Ozsurekci, Ayse Buyukcam, Ayse Gultekingil Keser, Ozlem Teksam, Mehmet Ceyhan Source Type: research

Acute peripheral facial paralysis following varicella infection: an uncommon complication
Chickenpox is caused by varicella zoster virus (VZV/HHV-3), which is one of the eight human herpes viruses. Although chickenpox has a good prognosis, neurologic complications including encephalitis, acute cerebellar ataxia, myelitis and meningitis may seldom be associated with the disease. Peripheral facial palsy (PFP) is an extremely rare complication in patients with chickenpox. Herein, we report a 12-year-old boy with chickenpox and unilateral peripheral facial palsy, who was successfully treated with short-term steroids and physical rehabilitation. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 10, 2016 Category: ENT & OMF Authors: Damla Hanalioglu, Yasemin Ozsurekci, Ayse Buyukcam, Ayse Gultekingil Keser, Ozlem Teksam, Mehmet Ceyhan Source Type: research

Recurrent neck abscess in a 2-year-old child
We report the case of an infant with recurrent neck infections despite appropriate treatment that was finally diagnosed as pyriform sinus fistula. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - February 10, 2016 Category: ENT & OMF Authors: María Soriano-Ramos, María Isabel González-Tomé, Elisa Fernández-Cooke, María Dolores Delgado-Muñoz, Eunate Martí-Carrera Tags: Case Report Source Type: research