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여환호,길병동,김운규 朝鮮大學校 口腔生物學硏究所 1989 口腔生物學硏究 Vol.13 No.-
Trigeminal neuralgia (tic douloureus', is a painful paroxysm of one of the branches(usually, the second or third division) of the trigeminal nerve, and the neuralgia may related to disseminated (multiple) sclerosis, to anoxia from vasospasm. or to ischemia from other casuses in the region of the gasserian ganglion or sensory root. Trigeminal neuralgia has been treated by drugs, nerve injections, surgery, and acupuncture. The drugs used in the past, such as as diphenylhydantoin(Dilantin), have largely been supplanted by carbamazepine(Tegretol), and it has proven remarkably effective in controlling the pain of trigeminal ueuralgia. Nerve blocks of the trigeminal ganglion that use alcohol, phenol, or hot water have also been reported to bring relief. Trigeminal tractotomy may or may not relieve the condition. However, surgical division of the sensory root in the medulla oblongata gives permanent relief. Other forms of treatment include trigeminal decompression and percutaneous electrocoagulation to cauterize the trigeminal nerve. Peripheral neurectomy is an effective treatment of trigeminal neuralgia because it interrupts the flow of a significant number of afferent impulses to the central trigeminal apparatus. We had performed peripheral neurectomy in a case. The pain free period obtained by peripheral neurectomy and the drugs (carbamazepine) in patient with trigeminal neuralgia and orofacial pain is significant. The purpose is to report our observatoni on the case report and the effectiveness of peripheral neurectomy of buccal nerve.
문행규,박용근,길병동 朝鮮大學校 口腔生物學硏究所 1988 口腔生物學硏究 Vol.12 No.-
Fibrous dysplasia is a skeletal developmental anomaly of unknown etiology with no appirent familial, hereditary, or congental basis, characterized by single or multiple areas of fibrous tissue replacement of medullary cavity of one or more bones. This disease is classified with monostotic and polyostotic fibrous dysplasia to those forms of the disease in which one or more than one bone is involved. The majority of mild case are simply treated by a cosmetic and conservative removal of the lesion contributing to the facial deformity and severe cases are impassible to terat in method is hazardous because of the possibility of subsequent malignant transformation. Twenty-one cases of fibrous dysplasia diagnosed by roentgenologic or histolotic assessments at Chosun Univ. Dental hospital during recent eight years(1979∼1986) were analyzed.
Yeo,Hwan Ho,Moon,Haeng Gyu,Kill,Beug Dong,Kim,Woon Gyu 大韓顎顔面成形再建外科學會 1989 Maxillofacial Plastic Reconstructive Surgery Vol.11 No.2
The ameloblastoma is the most common form of the odontogenic tumors exhibiting minimal inductive change in connective tissue, it comprising 1% of all tumor and cysts of the jaws. It is a true neoplasm, generally considered to be a benign but persistent or, locally malignant lesion. The tumor occurs most commonly in persons between the age of 20 and 50 years. 80% and 90% of all lesions are in the mandible. The presenting clinical signs and symptoms of the ameloblastoma very from patient to patient, but most common symptom was swelling, followed by pain, draining sinuses, and superficial ulcerations. It is slow-growing lesion, and the radiographic features of the ameloblastoma depend large one the nature and the local bone reaction to the particular tumor. Recurrence rate is about 33%, but this is probably due to incommplete intial removal of lesion. We had operated a patient ; 29-year-old female immediate reconstruction combined with autocompression plate and iliac bone graft and screw fixation after hemimandibulaectomy with recurred ameloblastoma involving from premolar to ascending ramus at right side mandible. We obtained favorable results of good function, short intermaxillary fixation periods and easy operation precedure than the other reconstruction methods.
Le Fort Ⅰ maxillary advancement and expansion in a bilateral alveolo-palatal cleft patient
문행규(Hang Gyu Moon),여환호(Hwan Ho Yeo),길병동(Byung Bong Kill),김일호(Il Ho Kim) 대한구강악안면외과학회 1989 대한구강악안면외과학회지 Vol.15 No.1
토순 및 구개파열환자의 부정교합은 골과 연조직의 결핍, 선천적 치아결손, 조기수술로 인한 반흔조직이 원인이 되며, 륵히 악궁의 비정상적인 힘의 영향으로 상ㆍ하악골의 부조화를 초래하여, 발육 또한 비정상적이 되고 부정교합의 영향이 더욱 심해지면서 안모의 부조화를 이루는 경우가 많다. 본 증례는 생후 11개월과 2년에 각각 양측성 토순과 양측성 구개열을 외과적으로 치료한 기왕력이 있는 17세된 남자 환자로서 부정교합 및 함몰형 측모를 주소로 내원한 바 상악골 수평골 절단술을 이용하여 상악골 전진 및 확장을 하면서 자가골 이식술을 시행하여 지견을 얻었기에 문헌고찰과 함께 보고드리는 바이다. 1. 영아ㆍ유아기에의 초기 외과적 처치 전후 계속 관찰하면서 차단성 악정형 처치의 필요성을 재 인식 하였고 2. 외과적으로 확장된 구개열 부위의 골이식은 palatal splint의 도움으로 재생능력과 위치 안정 성에 효과가 있었으며 3. Le Fort Ⅰ 골절단술을 통한 상악골 전진후 나타날 수 있는 발음의 비음화는 관찰할 수 없었 다.