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오래된 안와 내벽 골절이 동반된 만성 부비염에서 동시에 시행한 안와 내벽 골절 정복술 및 내시경 수술 1예
한정욱,석상혁,임준식,권기승 대한이비인후과학회 부산,울산,경남 지부회 2014 임상이비인후과 Vol.25 No.2
Minor and major complications can occur during endoscopic sinus surgery. Damage to an anatomic structure ad-jacent to a sinus is always a possibility during ESS. The lamina papyracea is very thin and may be fractured withrelatively minor truma. The presence of orbital fat, as well as the distorted anatomy at the fracture site, may makeendoscopy sinus surgey difficult or impossible because orbital fat is a landmark that surgeons should not crossfor fear of injury to orbital content, such as extraocular muscles, vasculature, and neural structures. If there maybe combined disruption of the medial orbital wall with orbital blowout fracture, orbital complication after ESSmay be very high. We report a case of endoscopic sinus surgery of chronic sinusitis and nasal polyps associatedold medial blowout fracture with a review of literature.
한정욱,임준식,김용완,백무진 대한이비인후과학회 부산,울산,경남 지부회 2014 임상이비인후과 Vol.25 No.2
Osseous choristoma is an extremely rare lesion of the oral cavity. It occurs usually in the tongue and exclusively in the flat bones of the skull. It is asymptomatic and only present when there is a disruption in the function of the organ due to its large size as it grows. A 61-year-old female was referred From neurologic department to ENT clinic because of tongue mass found accidentally. We tried surgical excision and the histopathologic report was osseous choristoma. So We report a case of osseous choriostoma with review of the literature.
중비갑개 및 비중격을 광범위하게 침범한 섬유성 이형성증 환자에서 비강 재건술 1예
한정욱,석상혁,임준식,권기승 대한이비인후과학회 2015 대한이비인후과학회지 두경부외과학 Vol.58 No.7
Fibrous dysplasia is a benign pathological condition of bone in which fibrous tissue gradually expands and replaces normal bone. Histologically, it shows various degrees of osseous metaplasia. Fibrous dysplasia frequently affects the maxilla, frontal bone, and mandible. The sign and symptoms of fibrous dysplasia of head and neck vary and are related to the location and extent of bony abnormalities. Facial asymmetry is the most common sign of fibrous dysplasia, while pain and ocular proptosis are the next most frequent symptoms. Fibrous dysplasia is rare in the nasal cavity, especially involving the turbinate and nasal septum. So we report a case of fibrous dysplasia, which extensively involves the middle turbinate and nasal septum, with a review of literature.
한정욱,정태영,박태정,김보영 대한이비인후과학회 부산,울산,경남 지부회 2010 임상이비인후과 Vol.21 No.1
Post-obstructive pulmonary edema (POPE) is an uncommon complication which develops immediately after the onset of acute airway obstruction or after the relief of chronic upper airway obstruction. Otolaryngologist frequently handles the upper airway, so the full knowledge about the mechanism and treatment of POPE for them is very important. We encountered a 33-years-old man with POPE after operation for obstructive sleep apnea and report this case with a review of the related literatures.
한정욱,권재환,김주연 대한이비인후과학회 부산,울산,경남 지부회 2012 임상이비인후과 Vol.23 No.2
The nasopalatine duct cyst is the most common cyst of nonodontogenic origin in the maxilla. It occurs approximately 1% of the population. Currently, it’s origin is thought to be from oronasal ducts within the incisive canal, however it is still a source of controversy. The etiology still remains unknown. Possible causes include trauma, infection, spontaneous proliferation. Symptoms were reported include swelling, drainage and pain. Radiographically, nasopalatine duct cyst usually appear as a round , ovoid or heart shaped radiolucent mass in the anterior palate. Surgical enucleation is the recommended treatment. However, if the size of cystic is above 2 cm and there is a risk of oroantral fistula after enucleation, marsupialization is indicated. The authors report a case of a large nasopalatine duct cyst which is treated with endoscopic marsupialization.
악하선관 결석 환자에서 발견된 일측성 악하선 무형성 1예
한정욱,정태영,박태정,문정환 대한이비인후과학회 부산,울산,경남 지부회 2010 임상이비인후과 Vol.21 No.2
The congenital absence of major salivary glands is an extremely rare disorder. The cause of congenital absence of the salivary glands has not been determined, but it may be associated with ectodermal defects of the first and second branchial arches. The etiopathogenesis of isolated absence of a major salivary gland without other developmental anomalies is still unclear. Unilateral aplasia of the submanibular gland with sialolithiasis of contralateral wharton’s duct has not been reported previously. The authors report with relative literature one case of Unilateral aplasia of the submanibular gland with sialolithiasis of contralateral Wharton’s duct. (J Clinical Otolaryngol 2010;21:279-282)