기저세포모반 증후군의 1례보고

• 영문명: A CASE REPORT OF BASAL CELL NEVUS SYNDROME
• 발행기관: 대한구강악안면외과학회
• 저자명: 류동목(Dong-Mok Ryu) 최병준(Byung-Jun Choi) 이상철(Sang-Chull Lee) 김여갑(Yeo-Gab Kim) 이백수(Baek-Soo Lee)
• 간행물 정보: 『대한구강악안면외과학회지』대한구강악안면외과학회지 제28권 제2호, 136~140쪽, 전체 5쪽
• 주제분류: 의약학 > 내과학
• 파일형태: PDF
• 발행일자: 2002.04.30

영문 초록

Basal cell nevus syndrome is inherited as an autosomal dominant trait with variable expressivity. This syndrome comprises a number of abnormalities such as multiple nevoid basal cell carcinomas of the skin, skeletal abnormalities as bifid rib and fusion of vertebrae, central nervous system abnormalities as mental retardation, eye abnormalities, and multiple odontogenic kerato cysts. In 1960, Gorlin and Goltz first described the features of this disease as constituting a true syndrome; since then, it has been realized that it is much more complex and encompassing than initially thought. This patient has many symtoms of basal cell nevus syndrome. - we has known multiple jaw cysts through panorama and facial computed tomography. He has hyperchromatism on basal cell through skin biopsy. In ophthalmologic consult, he has blindness on right. On his past medical history, amputation was done on his toes for polyductalism. - So we report with literature reviews

키워드

Basal Cell Nevus Syndrome Odontogenic Cysts