Gastrointestinal stromal tumours in pediatrics: A summary of the literature on this orphan disease

被引:0
|
作者
Verschuur, Arnauld [1 ]
Andre, Nicolas [1 ]
Blay, Jean-Yves [2 ]
机构
[1] Hop Enfants La Timone, Serv Oncol Pediat, F-13385 Marseille 5, France
[2] Ctr Leon Berard, Dept Med Oncol, F-69373 Lyon, France
关键词
GIST; children; adolescents; Carney triad; KIT; OF-THE-LITERATURE; PULMONARY CHONDROMA; MOLECULAR-FEATURES; GERMLINE MUTATION; CARNEY TRIAD; YOUNG-ADULTS; FOLLOW-UP; KIT GENE; GIST; PARAGANGLIOMA;
D O I
10.1684/bdc.2010.1296
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recommendations for the management of gastrointestinal stromal tumours (GIST) in children and adolescents do presently not exist. Thus, a summary of the current literature was conducted serving as a basis for the development of optimal management strategies for childhood GIST. Pediatric cases of GIST may occur sporadically, or within a predisposition syndrome such as Carney triad or Carney-Stratakis syndrome. Moreover, cases with familial GIST have been reported. The frequency of mutations of the oncogenes KIT and PDCFR alpha in sporadic GIST is substantially lower as compared with adults with GIST. An international prospective registration based on national registries has recently been started in order to acquire more clinical and molecular data and to develop appropriate management strategies for children and adolescents with GIST. Delta
引用
收藏
页码:79 / 86
页数:8
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