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하악결손증 태아에서 기도확보를 위해 시행한 EXIT 시술 1례
봉정표,김유정,양종원,김진형,김태환,최성진,Bong Jeong Pyo,Kim Yoo Jung,Yang Jong Won,Kim Jin Hyung,Kim Tae Hwan,Choi Seong Jin 대한기관식도과학회 2005 大韓氣管食道科學會誌 Vol.11 No.1
This study aimed to report a case of infant who presented with a prenatal ultrasound diagnosis of agnathia, polyhydramnios followed by a review of previous studies. As widely acknowledge, agnathia is a complex lethal malformation characterized by absent mandible, microstomia, microglossia and ear anomaly which are secondary results to a defect of the first branchial auh. Newborn infants with agnathia often suffer from airway obstruction, causing fatal respiratory failure. The most difficult part of treating those newborns is to keep the airway patent. Therefore, as early airway management planning as possible is the most important part. Airway management was achieved with tracheotomy through an ex utero intrapartum treatment procedure(EXIT). The case of this infant, reporting here, was underwent tracheotomy with preservation of uteroplacental blood flow and gas exchange.
봉정표,박장혁,최해명,김진형,이광길,엄민섭 대한이비인후과학회 2002 대한이비인후과학회지 두경부외과학 Vol.45 No.6
Myoepithelial cells are a significant component of most types of salivary gland neoplasms, but, pure myoepitheliomas are rare, comprising less than 1% of all salivary gland tumors. Malignant myoepithelioma, or myoepithelial carcinoma, is even more rare. It occurs most frequently in the parotid gland among salivary glands, and is similar to benign myoepitheliomas. surgical excision is the mainstay of therapy. The role of radiation therapy and chemotherapy is not yet established. We pr-esent a case of malignant myoepithelioma of the left parotid gland in a 67-year-old female patient who was treated with surgical excision folowed by adjuvant radiation therapy. (Korean J Otolaryngol 2002;45:624-7)
봉정표,김태환,이승조,김기택,성기준,정순희 대한이비인후과학회 2002 대한이비인후과학회지 두경부외과학 Vol.45 No.6
Myxolipomas, or myxoid lipomas, are unusual histologic types of lipoma in which components of the tumor are replaced by mucoid substances. Lipomas of the parapharyngeal space are extremely rare with only a few cases having been reported. The presence of myxolipoma in the parapharyngeal space has not yet been reported in the literature. We present the first report of (Korean J Otolaryngol 2002;45:620-3)