• J Craniofac Surg · Nov 2011

    Case Reports

    Surgical treatment of a giant neurofibroma.

    • Xiao-Bing Cheng, 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, and Lei Shen.
    • The Fourth Military Medical University. xiaobingcheng828@yahoo.com
    • J Craniofac Surg. 2011 Nov 1; 22 (6): 2244-6.

    AbstractNeurofibromatosis 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.

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