The management of orbitofacial neurofibromatosis.

Annals of plastic surgery 1982 Vol.8(3) p. 213-20

Van der Meulen JC, Moscona AR, Vandrachen M, Hirshowitz B

관련 도메인

Abstract

Neurofibromatosis is a rare inherited disease that may present as facial hamartoma or as a more generalized disease with subcutaneous tumors, skin pigmentation in the form of café-au-lait patches, and multiple pedunculated neurofibromas on a narrow skin base. The generalized form of the disease is named after von Recklinghausen, who described its main features in 1882. In this paper, we restrict ourselves to a discussion of the craniofacial manifestation of the disorder and also report our experience in treating 2 patients with orbitofacial neurofibromatosis at the Rambam Medical Center in Haifa.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
해부 subcutaneous 피하조직 dict 1
해부 orbitofacial scispacy 1
해부 skin scispacy 1
합병증 pigmentation 색소침착 dict 1
합병증 facial hamartoma scispacy 1
합병증 craniofacial scispacy 1
질환 orbitofacial neurofibromatosis scispacy 1
질환 Neurofibromatosis C0085113
NF1 gene
scispacy 1
질환 hamartoma C0018552
Hamartoma
scispacy 1
질환 tumors C0027651
Neoplasms
scispacy 1
질환 neurofibromas C0027830
neurofibroma
scispacy 1
질환 Recklinghausen C0027831
Neurofibromatosis 1
scispacy 1
질환 disease scispacy 1
질환 subcutaneous tumors scispacy 1
질환 von Recklinghausen scispacy 1

MeSH Terms

Child, Preschool; Facial Neoplasms; Female; Humans; Neurofibromatosis 1; Orbital Neoplasms; Surgery, Plastic

🔗 함께 등장하는 도메인

이 논문이 속한 카테고리와 같은 논문에서 자주 함께 다뤄지는 카테고리들

관련 논문