Gastrointestinal Stromal Tumors with KIT Mutation Coexisting with Wild-type Gastrointestinal Stromal Tumors in a Patient with Neurofibromatosis Type 1

Chin Med J (Engl). 2018 Sep 20;131(18):2244-2245. doi: 10.4103/0366-6999.240814.

Authors

Yang Li¹, Zhi-Dong Gao², Xiao-Dong Yang², Ying-Jiang Ye², Shan Wang¹, Ke-Wei Jiang²

Affiliations

¹ Laboratory of Surgical Oncology, Peking University People's Hospital, Beijing 100044, China.
² Department of Gastrointestinal Surgery, Peking University People's Hospital, Beijing 100044, China.

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Aged
Female
Gastrointestinal Neoplasms / genetics
Gastrointestinal Stromal Tumors / genetics*
Humans
Mutation / genetics
Neurofibromatosis 1 / genetics*
Proto-Oncogene Proteins c-kit / genetics*
Receptor, Platelet-Derived Growth Factor alpha / genetics

Substances

Proto-Oncogene Proteins c-kit
Receptor, Platelet-Derived Growth Factor alpha