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Pure esophageal atresia. 2 case
정상석,최필조,박권재,방정희,조광조,우종수,정진아,Jeong, Sang-Seok,Choi, Phil-Jo,Park, Kwon-Jae,Bang, Jung-Hee,Cho, Gwang-Jo,Woo, Jong-Soo,Jung, Jin-A 대한기관식도과학회 2008 大韓氣管食道科學會誌 Vol.14 No.1
Pure esophageal atresia without tracheoesophageal fistula is a uncommon form of congenital malformation of the esophagus, which is able to be suspected by fetal ultrasonograpy before delivery and diagnosed definitely by simple chest X-ray and esophagogram immidiately after delivery. We performed delayed primary repair in 2 cases of pure esophageal atresia by using stomach for conduit in one case and colon in the other case. But there were graft failure in the latter case, so reoperation was performed by using stomach. Postoperatively, two patients showed no stenosis and leakage in anastomotic site and were discharged in good oral intake without dysphagia.
박권재 ( Kwon Jae Park ),박창민 ( Chang Min Park ),정상석 ( Sang Seok Jung ),방정희 ( Jung Hee Bang ) 대한외상학회 2014 大韓外傷學會誌 Vol.27 No.3
Hypopharyngeal perforation is a rare, but fatal, complication. Clinical signs and symptoms of this condition are neck pain, odynophagia, dysphagia, fever, vomiting, cervical swelling and subcutaneous emphysema. However, these signs are obscured in patient suffering from severe trauma who has had an endotracheal tube inserted, which delay proper evaluation and treatment. Here, we report a case of hypopharyngeal perforation in a trauma patient who had an endotracheal tube inserted for mechanical ventilation. [ J Trauma Inj 2014;27:75-78 ]