Congenital atresia of posterior choanae.
نویسندگان
چکیده
Congenital atresia of posterior choanae is a moderately rare condition, and although Boyd (1945) has accounted for 230 cases in the literature, description of the symptoms presenting at birth are very scanty. Unilateral choanal obstruction is very much more common than the complete bilateral obstruction that was found in the present case. Richardson (1913) described a similar case in which relays of assistants maintained an airway by keeping the mouth of the child open, until at the end of a fortnight oral breathing was established.
منابع مشابه
A rare case report of bilateral choanal atresia in an adult
INTRODUCTION Adult choanal atresia is a rare congenital malformation of the nasal cavity characterized by the complete obliteration of the posterior choanae, only ninth cases are reported in the literature, we present in our observation the tenth case of adult bilateral choanal atresia. PRESENTATION OF CASE A 18-year-old man presented at our department with complaints of nasal obstruction, na...
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Congenital posterior choanal atresia is an uncommon anomaly which may have lifethreatening consequences. This defect is frequently associated with other congenital abnormalities. CT scan confirms the diagnosis and accurately defines the anatomy of the atresia and differentiates osseous stenosis from membranous stenosis in the choanae. Therefore, CT may be the first-line imaging choice for the p...
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OBJECTIVE To evaluate the short- and long-term success of the repair of congenital choanal atresia using the transnasal endoscopic approach with and without power instruments. DESIGN AND SETTING Retrospective case series in a tertiary care center. PATIENTS Fifteen patients with either unilateral or bilateral congenital choanal atresia were treated using the transnasal endoscopic approach. P...
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ورودعنوان ژورنال:
- Archives of disease in childhood
دوره 23 115 شماره
صفحات -
تاریخ انتشار 1948