Transnasal Endoscopic Repair of Congenital Choanal Atresia: a Case Report

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منابع مشابه

Transnasal endoscopic repair of congenital choanal atresia: long-term results.

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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Choanal atresia: Experience with transnasal endoscopic technique.

Congenital choanal atresia has been recognized for over 200 years, first described by Roederer in 1775 (Lantz and Brick, Laryngoscope 91, 1981, 1626. Samuel and Fernandes. Laryngoscope 95, 1985, 326). This condition is unconunon, occurring in approximately 1 in 7000 live births. Unfortunately, a single ideal procedure for this condition does not exist. Stankiewicz is credited with the first des...

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Case Report Congenital Bilateral Choanal Atresia

Congenital choanal atresia (CCA) is the developmental failure of the nasal cavity to communicate with nasopharynx. Surgical repair is recommended in the first weeks of life in bilateral cases because this is a lifethreatening situation in newborns. This is a case report of a full term, healthy newborn baby presenting with intermittent attacks of cyanosis and respiratory distress soon after birt...

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Transnasal endoscopic treatment of choanal atresia without prolonged stenting.

OBJECTIVE To analyze the outcome of transnasal endoscopic repair of choanal atresia (CA) in children without prolonged nasal stenting after surgery. DESIGN Retrospective study. SETTING Academic tertiary care children's hospital. PATIENTS Forty children aged 3 days to 15 years (mean age, 41 months) who presented with unilateral (n = 26) or bilateral (n = 14) CA and underwent surgery betwee...

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Congenital Bilateral Choanal Atresia: A Rare Case

Congenital Choanal Atresia (CCA) is the developmental misstep or inadequacy of the nasal cavity to connect posteriorly with the nasopharynx. Bilateral atresia presents with life threatening asphyxia at birth, while unilateral variety often remains unnoticed and presents later. This is to highlight the importance of taking into account the bilateral form in differential diagnosis of severe respi...

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ژورنال

عنوان ژورنال: Nihon Bika Gakkai Kaishi (Japanese Journal of Rhinology)

سال: 2010

ISSN: 0910-9153,1883-7077

DOI: 10.7248/jjrhi.49.490