RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      검색결과 좁혀 보기

      • 좁혀본 항목

      • 좁혀본 항목 보기순서

        • 원문유무
        • 음성지원유무
          • 원문제공처
          • 등재정보
          • 학술지명
          • 주제분류
          • 발행연도
          • 작성언어
          • 저자

        오늘 본 자료

        • 오늘 본 자료가 없습니다.
        더보기
        • 무료
        • 기관 내 무료
        • 유료
        • KCI등재

          Silver Diamine Fluoride의 치아우식 예방 효과

          송지수(Ji-Soo Song) 대한치과의사협회 2018 대한치과의사협회지 Vol.56 No.8

          Silver diamine fluoride (SDF) is an alkaline topical solution and it derives from the conjunction of silver nitrate and fluoride. It reduces the growth of cariogenic bacteria, inhibits degradation of dentinal collagen, impedes demineralization and enhances remineralization. It is inexpensive due to the low cost of materials and its application to dental surface is very simple and requires relatively short chair time. Previous studies have shown that the dental caries prevention effect of SDF is superior or similar to topical fluoride application. The main disadvantage of SDF is its esthetic result, and it permanently blacken carious enamel and dentin. The use of SDF has not yet been approved in Korea, but it may be helpful to prevent and treat dental caries in patients with special health care needs and uncooperative young patients.

        • CATCH22 syndrome 환아의 전신마취 하 치아우식 치료

          김민진(Min Jin Kim), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 현홍근(Hong-Keun Hyun) Asia association of Disability and Oral health 2018 대한장애인치과학회지 Vol.14 No.1

          CATCH22 syndrome or DiGeorge syndrome is a medical acronym of cardiac defects, abnormal facial appearances, thymic hypoplasia, cleft palate, and hypocalcemia. Patients with CATCH22 syndrome are susceptible to infection due to an absent or hypoplastic thymus and often have difficulties in maintaining good oral hygiene, which may require dental treatment. We present a case of dental treatment for the uncooperative child with CATCH22 syndrome under general anesthesia. A 4-year-old, 14.8 kg boy with CATCH22 syndrome visited Seoul National University Dental Hospital for dental check up. The patient had multiple caries requiring dental treatment. He experienced the corrective heart surgery due to Tetralogy of Fallot a few years ago. General anesthesia was planned because his heart rate and vital sign had shown unstable during the previous conscious sedation procedure. Dental restorative treatments were successfully performed and no complications were observed during and after the procedure. Safe and effective dental management of the patients with CATCH22 syndrome could be performed with the help of general anesthesia and careful monitoring.

        • 윌리엄스 증후군(Williams syndrome) 환자의 전신마취 하 치과치료

          서미경(Meekyung Seo), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 현홍근(Hong-Keun Hyun), 김정욱(Jung-Wook Kim), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 김영재(Young-Jae Kim) Asia association of Disability and Oral health 2018 대한장애인치과학회지 Vol.14 No.1

          Williams syndrome (WS) is a rare congenital disorder which is caused by microdeletion of approximately 1.6 MBP from the long arm of chromosome 7 at 7q11.23. It is characterized by cardiovascular anomalies, elfin face and mental retardation. The most typical oral signs in patient with WS are hypodontia, reduced mesio-distal dimensions both in the primary and permanent teeth, macroglossia, excessive interdental spacing, enamel hypoplasia and enamel hypomineralization. The majority of children with WS have mild to moderate mental retardation, generalized anxiety disorder, hyperactivity disorder and sensitivity to sounds. The purpose of this presentation is to describe dental treatment for a child with WS. A 9-year-old boy diagnosed with WS had caries on his first permanent molars. Because of the poor cooperation, these teeth were filled temporarily with glass ionomer, and treatment under general anesthesia was planned. Under general anesthesia, caries treatment of first permanent molar and extraction of primary molar was successfully performed and there was no postoperative complications related to general anesthesia. Open bite, hypodontia, excessive dental space, enamel hypoplasia, enamel hypomineralization were observed which were characteristic in WS.

        • Lennox-Gastaut syndrome 환아의 전신마취 하 치아우식 치료

          서희원(Heewon Suh), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 현홍근(Hong-Keun Hyun), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 이상훈(Sang-Hoon Lee), 장기택(Ki-Taeg Jang) Asia association of Disability and Oral health 2018 대한장애인치과학회지 Vol.14 No.1

          Lennox-Gastaut syndrome (LGS) is one of the most severe epileptic encephalopathies of childhood onset. It is characterized by multiple types of generalized seizures, slowness of intellectual growth, and specific electroencephalogram pattern. It is one of the most difficult epilepsy syndromes to treat and is frequently resistant to treatment. In this case report, we report a case of dental treatment under general anesthesia in a child with LGS. A 4-year-6-month old boy with LGS visited Seoul National University Dental Hospital for dental treatment. Dental treatment was planned under general anesthesia because of his medical condition. Treatment was successfully done without any postoperative complications. If a LGS patient requires dental treatment, a treatment plan should be established to take into account the degree of seizure, the medication being used, and the cooperation of the patient. If the degree of seizure is severe and the patient's cooperation is poor, dental treatment under general anesthesia would be advantageous.

        • 모야모야병(moyamoya disease) 환자의 전신마취 하 치과 치료

          상은정(Eun Jung Sang), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 김영재(Young-Jae Kim), 김정욱(Jung-Wook K), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 현홍근(Hong-Keun Hyun) Asia association of Disability and Oral health 2017 대한장애인치과학회지 Vol.13 No.2

          Moyamoya disease is a disorder in which certain arteries in the brain are constricted. Blood flow can be blocked by the constriction and blood clots. The patients frequently experience transient ischemic attacks (TIA), cerebral hemorrhage, or may not experience any symptoms at all. It is reported that they have a higher risk of recurrent stroke and a distinct underlying pathophysiology. A 3-year-8-month old boy with moyamoya disease experienced cerebral infarctions five times, and he underwent a cerebrovascular anastomosis surgery four years ago. He showed swallow disturbance, general delayed development, hemiplegia, and strabismus. Also he had hypocalcified teeth with or without multiple caries lesions in all dentitions. Dental treatment under general anesthesia using sevoflurane was performed due to his lack of cooperation. Moyamoya disease is associated with various medical conditions requiring a thoughtful deliberation and a careful examination before and during dental treatment. Pain and anxiety control during dental treatment is important because hyperventilation induced by crying has been seen to trigger TIA. Both isoflurane and sevoflurane are commonly used in patients with MMD, but dynamic autoregulation is better preserved during sevoflurane than isoflurane anesthesia. So sevoflurance general anesthesia may be recommendable to manage dental patients having multiple caries with moyamoya disease.

        • Bartter 증후군 환아의 치아우식 치료: 증례보고

          김민지(Minji Kim), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 현홍근(Hong-Keun Hyun), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 이상훈(Sang-Hoon Lee), 장기택(Ki-Taeg Jang) Asia association of Disability and Oral health 2019 대한장애인치과학회지 Vol.15 No.1

          Bartter 증후군은 심각한 헨레고리 비후 상행각(TAL)에서의 일차적인 염류(NaCl) 수송 장애로 인하여 심각한 저칼륨혈증을 특징으로 하는 질환이다. 만성 구토로 인한 치아의 부식, 교모, 마모의 구강 내 소견을 보여 구토와 관련된 적절한 칫솔질 및 식이 습관 등에 대한 정기적인 교육과 관찰이 권장되며 교합고경의 회복을 위해 전장관 수복이 추천된다. 치과 치료 시의 스트레스로 인하여 전해질 수치의 불균형이 초래될 가능성이 있어 전신마취 하 치료가 유리할 수 있으며, 전신마취 시 과환기되어 저칼륨혈증이 심화되지 않도록 지속적인 감시를 해야하고 술 후에도 전해질 불균형이 초래되지 않도록 지속적인 감시가 필요하다. Bartter syndrome is an inherited renal tubular disorder characterized by hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia, hyperprostaglandinism, and normal blood pressure. Bartter syndrome is classified by neonatal and classic type. Clinical manifestation of Bartter syndrome considered in dental treatment include tendency to dehydration, vomiting and erosion, attrition and abrasion of the teeth. A 2-year-4 month old boy with Bartter syndrome type III was referred to the Seoul National University Dental Hospital for dental evaluation and treatment. He showed hypokalemic hypochloremic metabolic alkalosis and had been treated with indomethacin and potassium chloride. He had hypocalcified teeth with or without multisurface caries lesions in all dentition and the erosion of maxillary teeth was detected. Dental procedure under general anesthesia was scheduled due to multiple caries and his medical condition. The dental procedure was successfully performed. This case suggests that electrolyte imbalances need to be treated prior to dental treatment and complete coverage restoration is necessary to protect the eroded teeth. An appropriate management plan for the patients with Bartter syndrome should include considerations of the need for close interaction with the pediatrician for pre- and post-operative care. General anesthesia may be recommendable to manage the patients having multiple caries with Bartter syndrome.

        • 선천성 범뇌하수체저하증(Congenital panhypopituitarism) 환자의 전신마취 하 치과치료

          김현태(Hyuntae Kim), 송지수(Ji-Soo Song), 현홍근(Hong-Keun Hyun), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 신터전(Teo Jeon Shin) Asia association of Disability and Oral health 2019 대한장애인치과학회지 Vol.15 No.1

          선천성 뇌하수체저하증(Congenital panhypopituitarism)은 갖는 환자는 스트레스에 대한 대처 능력이 떨어지기 때문에 치과치료 전 발생할 수 있는 부신 급성발증(adrenal crisis)에 대해서 미리 대비하는 것이 중요하다 스트레스를 유발하는 치과치료 시행 시 호르몬 대체 요법의 시행을 고려해야 한다. 치과치료 전 환아의 연령과 전신상태를 고려하여 적절한 치료 방법을 선택해야 할 것이며 비정상적인 악안면 성장 패턴을 보일 가능성이 있으므로 성장관찰을 동반한 정기 검진이 요구된다. Congenital panhypopituitarism is an uncommon condition, present from birth, characterized by the decreased secretion of most of the hormones produced by the pituitary. The purpose of this case report is to present a case about caries treatment of a 26-month-old female patient with congenital panhypopituitarism under general anesthesia. A 26-month-old girl with congenital panhypopituitarism visited Seoul National University Dental Hospital for caries treatment of anterior primary teeth. Because of the child's age and underlying systemic disease, dental treatment under general anesthesia was considered. Prior to the dental procedure, 30mg of cortisol was administered intravenously in order to prevent possible adrenal crisis by stressful events. The dental procedure was successfully performed under general anesthesia. This case report suggests that general anesthesia may be useful for the dental treatment with congenital panhypopituitarism. Hormone deficiency should be assessed prior to dental procedure and, if necessary, stress hormone replacement therapy should be considered.

        • 비정형 유기형/간상 종양(Atypical teratoid rhabdoidal tumor) 환자의 전신마취 하 치과치료

          김현태(Hyuntae Kim), 송지수(Ji-Soo Song), 현홍근(Hong-Keun Hyun), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 신터전(Teo Jeon Shin) Asia association of Disability and Oral health 2019 대한장애인치과학회지 Vol.15 No.1

          AT/RT를 갖는 환자는 빈번하게 MRI촬영을 시행하게 된다. MRI 의 경우 강자성 효과(ferromagnetic effect)로 인해 스테인레스스틸 기성금속관의 탈락이 발생할 위험성이 있고 영상의 인공물(artifact)의 형성을 유발할 수 있으므로 유치의 전장관수복 전에 재료의 선택에 있어서 이러한 위험성에 대해 고려해야 한다. 이 경우 기성 지르코니아 전장관은 AT/RT 환자들의 크라운 수복에 있어서 좋은 수복재료로 사용될 수 있다. 또한 항암치료로 인해 AT/RT 환아들은 우식발생율이 높으므로 구강위생 관리 및 전문가 불소도포 등의 주기적인 정기검진이 요구된다. Atypical teratoid rhabdoidal tumor(AT/RT) is a rare and fast-growing tumor usually diagnosed in childhood. Routine magnetic resonance imaging(MRI) assessment of AT/RT patients is done to detect metastatic tumors and recurrent lesions. The purpose of this case report is to present a case about caries treatment of a 3-year-8-month old female patient with AT/RT under general anesthesia. A 3-year-8-month old patient with AT/RT visited Seoul National University Dental Hospital for caries treatment. At the first dental visit, she was receiving chemotherapy. Multiple caries were observed from clinical and radiographic examination. The dental procedure was successfully performed under general anesthesia. Patients with brain tumor may take routine MRI to detect metastatic tumors and recurrent lesions. Dentists should take into consideration of possible dislodgement of restoration by ferromagnetic properties and artifact formation on MRI image. Ready-made zirconia crowns can be a good restoration option for such patients.

        • Treacher Collins 증후군 환아의 치과 치료: 증례보고

          김민지(Minji Kim), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 현홍근(Hong-Keun Hyun), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 이상훈(Sang-Hoon Lee), 장기택(Ki-Taeg Jang) Asia association of Disability and Oral health 2019 대한장애인치과학회지 Vol.15 No.1

          Treacher Collins 증후군(TCS)은 두개안면 발육의 이상을 보이는 상염색체 우성 질환으로, 외이, 중이 및 이소골(auditory ossicle)의 형태이상과 상악골 발육 부전, 후퇴된 하악, 구개열등의 특징을 보인다. TCS 환아의 경우, 청각 장애로 인한 환아의 불안으로 적절한 협조를 얻기 어렵고, 개구제한과 기도 확보의 어려움으로 인해 전신마취 하에 치과치료를 진행하는 것이 안전하다. 전신마취 시 하악 후퇴 등의 형태학적인 문제로 인하여 삽관의 난이도가 높을 수 있어 주의가 요구되며, 술 후에도 적절한 호흡의 유지를 위해 지속적인 감시가 필요하다. 마지막으로, 보호자로 하여금 구강 위생의 중요성이 강조되어야 한다. Treacher Collins syndrome(TCS) is an autosomal craniofacial development disorder which results from mutations in the gene TCOF1. Major features include midface hypoplasia, micrognathia, microtia, conductive hearing loss. Oral manifestations are characterized by cleft palate, shortened soft palate, malocclusion, anterior open bite and enamel hypoplasia. The purpose of this presentation is to describe the interesting aspects of dental treatment of a patient with TCS. A 6-year-old boy with TCS visited Seoul National University Dental Hospital for dental caries. Multiple caries was observed from clinical and radiographic examination. Because of multiple caries and behavior management ploblem, dental treatment under general anesthesia was planned. Treatment of posterior teeth was performed and some primary teeth were extracted. General anesthesia was induced and maintained with sevoflurane, nitrous oxide and oxygen. Under general anesthesia, successful dental procedure was done. Considering behavior management problem and medical condition of patient with TCS, general anesthesia can be useful.

        • Lowe syndrome 환아의 전신마취 하 치아우식 치료: 증례보고

          김민진(Min Jin Kim), 송지수(Ji-Soo Song), 신터전(Teo Jeon Shin), 김영재(Young-Jae Kim), 김정욱(Jung-Wook Kim), 장기택(Ki-Taeg Jang), 이상훈(Sang-Hoon Lee), 현홍근(Hong-Keun Hyun) Asia association of Disability and Oral health 2019 대한장애인치과학회지 Vol.15 No.1

          Lowe Syndrome 환아는 안 질환, 근신경계 질환, 신장기능이상을 특징으로 하나 임상양상은 다양하게 나타난다. 본 증례는 이전에 악성 고열증 병력이 있었으며, 치과검진에 비협조적이고 다수의 치아 우식을 보이는 4세 6개월의 Lowe syndrome환자를 전정맥 전신마취 하에 효과적으로 치료하였기에 이를 보고하는 바이다. 연하장애로 인한 잦은 유동식섭취와 구토는 치아의 우식 활성과 부식을 가속화시킬 수 있어 보다 적극적인 구강위생교육과 적극적인 치료가 요구된다. Lowe syndrome 환아의 치과치료를 계획할 때에는 전신상태에 대한 충분한 이해 및 이전 전신마취에 대한 평가가 필수적으로 선행되어야 하며, 이전에 악성 고열증 병력이 있었던 경우 프로포폴을 이용한 목표농도 조절 주입법이 보다 안전하고 효과적인 방법이 될 수 있을 것으로 사료된다. Oculo-cerebro-renal syndrome, known as Lowe syndrome, is an X-linked gene disorder characterized by congenital cataracts, brain abnormalities and renal dysfunction. Tooth crowding, taurodontism, delayed eruption in the permanent dentition and over-retained primary teeth with ectopic eruption of the permanent teeth have been reported as dental findings. Because of the high incidence of poor cooperation, patients with Lowe syndrome have difficulties in maintaining good oral hygiene, which may require dental treatment. We present a case of dental treatment for the uncooperative child with Lowe syndrome under general anesthesia. A 4-year-old, 11.2 kg boy with Lowe syndrome visited Seoul National University Dental Hospital for gingival swelling. The patient had multiple caries requiring dental treatment. Because of his past history of malignant hyperthermia during inhalation induction, anesthesia was induced and maintained with total intravenous anesthesia (TIVA) after medical consultation. Dental restorative treatments were successfully performed and no complications were observed during and after the procedure. Safe and effective dental management of the patients with Lowe syndrome could be performed with the help of general anesthesia and careful monitoring.

        맨 위로 스크롤 이동