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

Gastrointestinal Stromal Tumors with KIT Mutation Coexisting with Wild-type Gastrointestinal Stromal Tumors in a Patient with Neurofibromatosis Type 1
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摘要 To the Editor: Neurofibromatosis type 1 (NFI) is one of the most common autosomal dominant inherited disorders with a prevalence of approximately 1 in 3000 individuals, Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. Studies have suggested that NF 1 associated GISTs (NF 1-GISTs) manifest at younger ages than sporadic GISTs. To the Editor: Neurofibromatosis type 1 (NFI) is one of the most common autosomal dominant inherited disorders with a prevalence of approximately 1 in 3000 individuals, Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. Studies have suggested that NF 1 associated GISTs (NF 1-GISTs) manifest at younger ages than sporadic GISTs.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第18期2244-2245,共2页 中华医学杂志(英文版)
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