Literature DB >> 22075824

Surgical treatment of a giant neurofibroma.

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.

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Year:  2011        PMID: 22075824     DOI: 10.1097/SCS.0b013e31823270cb

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  2 in total

1.  Unusual Evolution of Plexiform Neurofibroma in the Scalp: A Case Report.

Authors:  Amine Rafik; Mounia Diouri; Naima Bahechar; Abdessamad Chlihi
Journal:  World J Plast Surg       Date:  2018-01

2.  Lady with wings: a case report of giant neurofibromatosis type I.

Authors:  Suraj Maharjan; Xiucun Li; Jianli Cui; Yang Liu; Laijin Lu
Journal:  Medicine (Baltimore)       Date:  2017-07       Impact factor: 1.889

  2 in total

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