| Literature DB >> 22075824 |
Xiao-Bing Cheng1, De-Lin Lei, Yun-Peng Li, Lei Tian, Yan-Pu Liu, Xing-Hua Feng, Xiao-Guang Hu, Mo-Yi Sun, Qin Ma, Tian-Qiu Mao, Bao-Lin Liu, Yi-Min Zhao, Zhi-Hong Feng, Li-Xian Xu, Hui Zhang, Tie-Cheng Zhang, Rui Liu, Lei Shen.
Abstract
Neurofibromatosis type 1, an autosomal dominant inherited disease, presents pathologic symptoms of multiple systems, including neurofibromatosis, skeletal dysplasia, café-au-lait spots in skins, and so on. A 45-year-old man with neurofibromatosis type 1 was reported in this article. The patient presented a giant neurofibroma in his head and neck, dysplasia of skull, facial bones and spinal columns, and multiple café-au-lait spots in systematic skins. Satisfactory curative effects were obtained in this case after tumor resection and prosthesis implantation.Entities:
Mesh:
Year: 2011 PMID: 22075824 DOI: 10.1097/SCS.0b013e31823270cb
Source DB: PubMed Journal: J Craniofac Surg ISSN: 1049-2275 Impact factor: 1.046