Résumé
Les tumeurs stromales gastro-intestinales (GIST) n’étaient pas reconnues comme des entités cliniques distinctes en 1998, bien que plusieurs équipes d’anatomopathologistes aient rapporté depuis 1983 leur existence et leurs particularités phénotypiques en les désignant sous différents noms (GIST, GANT, GIPACT, ICCT…) (1). En 2009, dix ans après, cette tumeur est devenue le paradigme des maladies néoplasiques traitées par des thérapeutiques ciblées et les règles de leur prise en charge, toujours en rapide évolution, semblent pouvoir s’appliquer à des tumeurs plus fréquentes au-delà des sarcomes.
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Ray-Coquard, I., Cassier, P., El Sayadi, H., Blay, JY. (2010). Tumeurs stromales gastro-intestinales (GIST). In: Tumeurs malignes rares. Springer, Paris. https://doi.org/10.1007/978-2-287-72070-3_26
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DOI: https://doi.org/10.1007/978-2-287-72070-3_26
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