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Neurofibromatosis Type 1 Associated Gastrointestinal Stromal Tumors

  • Yao Lin,
  • Xiangyu Zeng,
  • Chengguo Li,
  • Zhidong Gao,
  • Jian Li

摘要

Neurofibromatosis type 1 (NF1), or von Recklinghausen disease, is an autosomal dominant genetic disease. Patients with NF1 are prone to develop various types of tumors, including GIST [1]. For patients with NF1, GIST mainly occur in the duodenum and jejunum. Multiple primary tumors and wild-type KIT and PDGFRA are the most significant features [2].