WITHDRAWN: Ectopic meningothelial hamartoma of the scalp associated with frontonasal dysplasia
This article has been withdrawn at the request of the author(s) and/or editor.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 - August 26, 2014 Category: ENT & OMF Authors: Daniel Thomas Ginat Source Type: research

Type IV laryngotracheoesophageal cleft with associated pulmonary foregut malformation
Laryngotracheoesophageal clefts are rare anomalies usually diagnosed in early infancy with high rates of morbidity and mortality. Frequent complications after repair are tracheoesophageal fistula, tracheomalacia, and tracheostomy dependence. Here we describe the successful repair of a Type IV laryngotracheoesophageal cleft with an associated bronchopulmonary foregut malformation in a full-term female infant. In addition to a three-layered closure, costal cartilage grafts were used anteriorly and posteriorly to recreate the lamina of the cricoid. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - August 26, 2014 Category: ENT & OMF Authors: Naveen Kumar, Michael Haupert, Phani Durvasula, Sonal Saraiya Tags: Case Report Source Type: research

Ectopic meningothelial hamartoma of the scalp associated with frontonasal dysplasia
Frontonasal dysplasia and ectopic meningothelial hamartoma of the scalp are both rare entities. The purpose of this report is to describe a unique case in which these anomalies are present simultaneously. CT showed a soft tissue mass with funnel shape morphology in the scalp overlying the posterior fontanelle and MRI shows a mildly enhancing T2 heterogeneous nodule without discernible intracranial extension. Ectopic meningothelial hamartomas should be considered in the differential diagnosis for a midline scalp mass, particularly when a lesion demonstrates a funnel shape morphology and enhancement. (Source: International J...
Source: International Journal of Pediatric Otorhinolaryngology Extra - August 26, 2014 Category: ENT & OMF Authors: Daniel Thomas Ginat Tags: Case Report Source Type: research

WITHDRAWN: Ectopic meningothelial hamartoma of the scalp associated with frontonasal dysplasia
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 - August 25, 2014 Category: ENT & OMF Authors: Daniel Thomas Ginat Source Type: research

List of Societies
(Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - August 24, 2014 Category: ENT & OMF Source Type: research

Two cases of intranasal foreign body which treatment results are extremely different
We report two cases of intranasal foreign body which treatment results were extremely different. Also, we suggest that the simple radiography can identify easily the property of the foreign body in cases of metallic foreign bodies. So, it is important to know about characteristic X-ray findings of metallic foreign bodies. Through this knowledge, a button battery and bilateral magnetic foreign bodies should be differentiated and removed as soon as possible. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - August 1, 2014 Category: ENT & OMF Authors: Ji Ho Shin, Kyung Soo Kim Tags: Case Report Source Type: research

Two cases of intranasal foreign body which treatment results are extremely different
We report two cases of intranasal foreign body which treatment results were extremely different. Also, we suggest that the simple radiography can identify easily the property of the foreign body in cases of metallic foreign bodies. So, it is important to know about characteristic x-ray findings of metallic foreign bodies. Through this knowledge, a button battery and bilateral magnetic foreign bodies should be differentiated and removed as soon as possible (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - August 1, 2014 Category: ENT & OMF Authors: Ji Ho Shin, Kyung Soo Kim Source Type: research

Extramedullary hematopoiesis of the paranasal sinuses associated with moyamoya syndrome in sickle cell disease
Sickle cell disease is a common blood disorder with well-known clinical presentations including extramedullary hematopoiesis and moyamoya syndrome. However, it is extremely rare for extramedullary hematopoiesis to occur in the paranasal sinuses. Here, we present a case of a child with known homozygous sickle cell disease who has extramedullary hematopoiesis within the maxillary and the sphenoidal sinuses associated with moyamoya syndrome. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - July 30, 2014 Category: ENT & OMF Authors: Anıl Özgür, Engin Kara, Gonca Çabuk, Selma Ünal, Meltem Nass Duce Tags: Case Report Source Type: research

Extramedullary hematopoiesis of the paranasal sinuses associated with moyamoya syndrome in sickle cell disease*
Sickle cell disease is a common blood disorder with well-known clinical presentations including extramedullary hematopoiesis and moyamoya syndrome. However, it is extremely rare for extramedullary hematopoiesis to occur in the paranasal sinuses. Here, we present a case of a child with known homozygous sickle cell disease who has extramedullary hematopoiesis within the maxillary and the sphenoidal sinuses associated with moyamoya syndrome. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - July 30, 2014 Category: ENT & OMF Authors: Anıl Özgür, Engin Kara, Gonca Çabuk, Selma Ünal, Meltem Nass Duce Source Type: research

Acquired glottic web formation in a 3-year-old girl: Case report and literature review
We report a unique variation of this post-traumatic etiology: a web centered at the junction of the anterior one-third and posterior two-thirds of the vocal folds, possibly formed after phonotraumatic stress from severe coughing. Our case suggests that careful attention should be paid to persistent voice changes after acute illness, as this may be a sign of laryngeal web in the setting of phonotraumatic stress. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - July 10, 2014 Category: ENT & OMF Authors: Susan D. Emmett, Lee M. Akst, Margaret L. Skinner Tags: Case Report Source Type: research

Pediatric inverted papilloma of the middle ear: Case report and review of the literature
We report a middle ear inverted papilloma in an 11-year-old male. To the best of our knowledge it is the first pediatric inverted papilloma of middle ear. The patient had a history of chronic suppurative otitis media and the lesion was found during preoperative evaluation for a tympanoplasty procedure. Total excision of the lesion and a tympanoplasty operation was accomplished. We reviewed the middle ear inverted papilloma cases regarding the age distribution, pathophysiology, treatment and prognosis. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - June 18, 2014 Category: ENT & OMF Authors: Burak Ulkumen, Yunus Kaplan, Ahmet Faruk Kıroglu, Irfan Bayram Tags: Case Report Source Type: research

A case of bilateral enlarged vestibular aqueducts and unilateral hearing loss at birth
Screening of newborn hearing is nowadays widespread, and as many as 3.4% of all screened infants are found to have unilateral hearing loss. However, we, as clinicians and parents, usually dismiss the severity of unilateral hearing loss in pediatric patients. Recently, we experienced the case of unilateral hearing loss since birth in a 2-year-old girl who was finally found to have bilateral enlarged vestibular aqueducts when the disorder progressed to bilateral hearing loss. Proper evaluation of the cause of hearing loss, including imaging studies of the inner ear, and consecutive hearing evaluations should be mandatory in ...
Source: International Journal of Pediatric Otorhinolaryngology Extra - June 12, 2014 Category: ENT & OMF Authors: Eun-Jung Lim, Hun-Po Cho, Jun-Ki Lee, Tae Hoon Kim, Jun Ho Park, SungHee Kim Tags: Case Report Source Type: research

Subglottic diffuse large B-cell lymphoma presenting as biphasic stridor
We report a case of a young child with acute onset biphasic stridor who was found to have a large subglottic lesion causing significant airway obstruction. We were able to successfully resect it to achieve a pathologic diagnosis and address the subglottic stenosis with an anterior laryngofissure followed by laryngotracheal reconstruction (LTR) using a rib graft. The final pathology was diffuse large B-cell lymphoma, anaplastic variant, and patient had complete response to chemotherapy and is currently free of disease. (Source: International Journal of Pediatric Otorhinolaryngology Extra)
Source: International Journal of Pediatric Otorhinolaryngology Extra - June 12, 2014 Category: ENT & OMF Authors: Wen Jiang, Denise M. Malicki, Amy E. Geddis Tags: Case Report Source Type: research