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      Role of Multislice Computed Tomography and Local Contrast in the Diagnosis and Characterization of Choanal Atresia

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      1 , * , 2
      International Journal of Pediatrics
      Hindawi Publishing Corporation

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          Abstract

          Objective. To illustrate the role of multislice computed tomography and local contrast instillation in the diagnosis and characterization of choanal atresia. To review the common associated radiological findings. Methods. We analyzed 9 pediatric patients (5 males and 4 females) with suspected choanal atresia by multislice computed tomography. We recorded the type of atresia plate and other congenital malformations of the skull. Results. Multislice computed tomography with local contrast installed delineated the posterior choanae. Three patients had unilateral mixed membranous and bony atresia. Three patients had unilateral pure bony atresia. Only 1 of 7 patients have bilateral bony atresia. It also showed other congenital anomalies in the head region. One patient is with an ear abnormality. One patient had congenital nasal pyriform aperture stenosis. One of these patients had several congenital abnormalities, including cardiac and renal deformities and a hypoplastic lateral semicircular canal. Of the 6 patients diagnosed to have choanal atresia, 1 patient had esophageal atresia and a tracheoesophageal fistula. The remaining patients had no other CHARGE syndrome lesions. Conclusions. Local Contrast medium with the application of the low-dose technique helps to delineate the cause of the nasal obstruction avoiding a high radiation dose to the child.

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          Most cited references20

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          Spiral volumetric CT with single-breath-hold technique, continuous transport, and continuous scanner rotation.

          Continuous computed tomographic (CT) scanning of organ volumes during a single breath hold was studied. The authors modified the table feed mechanism of a continuously rotating CT scanner to allow patient transport at low, but accurately controlled, speeds (0.1-11.0 mm/sec) during continuous 1-second scanning. An algorithm was designed to reconstruct artifact-free images for arbitrary table positions from the helical data by interpolating between adjacent scans. Section sensitivity profiles were enlarged; the section width for a 10-mm section and a speed of 10.0 mm/sec was increased by a factor of 1.3, compared with the nominal value. Clinical examples were presented for studies of lung nodules and studies enhanced with contrast medium. Major advantages are the possibility of continuous scanning of extended volumes within a breath-hold period and retrospective, arbitrary selection of anatomic levels.
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            Choanal atresia and choanal stenosis.

            Congenital narrowing of the nasal airway at the posterior choanae, which can be uni- or bilateral, is an uncommon condition in pediatric patients. The surgical management of choanal atresia varies widely in different centers. This article discusses the different surgical strategies including: dilation and stenting; trans-palatal repair; and transnasal resection utilizing endoscopic sinus surgery (ESS) techniques. The merits of stents, lasers, CT-guided surgery, and the use of additional agents including mitomycin C are reviewed, as well as the particular problems associated with managing bilateral choanal atresia in neonates.
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              Congenital nasal pyriform aperture stenosis.

              Congenital nasal pyriform aperture stenosis is an unusual and previously undescribed cause of nasal airway obstruction in the newborn. The nasal pyriform aperture is narrowed due to bony overgrowth of the nasal process of the maxilla. This anomaly may produce signs and symptoms of nasal airway obstruction in newborns and infants similar to those seen in bilateral posterior choanal atresia. Computed tomography confirms the diagnosis and delineates the anomaly. A series of six patients with nasal pyriform aperture stenosis is presented. Four patients were treated with surgical enlargement of the nasal pyriform aperture via a sublabial approach. One patient was repaired via a transnasal approach, and one patient did not undergo surgical intervention. Follow-up reveals normal nasal airway and facial growth in all patients. Mildly symptomatic patients with congenital nasal pyriform aperture stenosis may be treated expectantly, while severely symptomatic patients benefit from repair via the sublabial approach.
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                Author and article information

                Journal
                Int J Pediatr
                IJPED
                International Journal of Pediatrics
                Hindawi Publishing Corporation
                1687-9740
                1687-9759
                2011
                22 May 2011
                : 2011
                : 280763
                Affiliations
                1Department of Otolaryngology, King Abdulaziz University, P.O. Box 35135, Jeddah 21488, Saudi Arabia
                2Radiology Department, International Medical Centre, P.O. Box 2172, Jeddah 21451, Saudi Arabia
                Author notes
                *Khaled Al-Noury: kalnoury@ 123456yahoo.com

                Academic Editor: Joseph M. Croffie

                Article
                10.1155/2011/280763
                3134835
                21772853
                e6c854cc-79fa-4a11-812e-809db908208f
                Copyright © 2011 K. Al-Noury and A. Lotfy.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 5 January 2011
                : 9 March 2011
                Categories
                Clinical Study

                Pediatrics
                Pediatrics

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