神経線維腫症1型患者の口蓋に発生した巨大な神経線維腫の1例

Neurofibromatosis type I (NF1) is a chromosomal dominant hereditary disease characterized by cafe-au-lait spots of the skin and multiple neurofibroma. Oral manifestation of NF1 is relatively infrequent. We report a rare case of huge neurofibroma arising in the palate, associated with NF1. A 39-year-...

Full description

Saved in:
Bibliographic Details
Published in日本口腔外科学会雑誌 Vol. 67; no. 10; pp. 596 - 600
Main Authors 比嘉, 努, 比嘉, 盛敏, 狩野, 岳史, 銘苅, 泰明, 新垣, 敬一, 仲間, 錠嗣
Format Journal Article
LanguageJapanese
Published 社団法人 日本口腔外科学会 20.10.2021
Subjects
Online AccessGet full text
ISSN0021-5163
2186-1579
DOI10.5794/jjoms.67.596

Cover

More Information
Summary:Neurofibromatosis type I (NF1) is a chromosomal dominant hereditary disease characterized by cafe-au-lait spots of the skin and multiple neurofibroma. Oral manifestation of NF1 is relatively infrequent. We report a rare case of huge neurofibroma arising in the palate, associated with NF1. A 39-year-old woman visited our department with the complaint of a painless mass in the hard palate. An elastic-soft swelling measuring 50 x 38 mm was found on the right palate. The tumor was excised under general anesthesia. Histopathological findings revealed neurofibroma. The tumor has not recurred, and the patient has made good progress.
ISSN:0021-5163
2186-1579
DOI:10.5794/jjoms.67.596