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Gastrointestinal stromal tumour as a rare association with neurofibromatosis type 1
Gastrointestinal stromal tumours (GIST) are rare tumours of mesenchymal origin. These can be associated with neurofibromatosis type 1 (NF1), which is an autosomal dominant disorder. The prevalence of GIST in NF1 is estimated at 3.9–25%. This paper describes the presentation of a GIST arising from th...
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| Pubblicato in: | J Surg Case Rep |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5822698/ https://ncbi.nlm.nih.gov/pubmed/29492250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jscr/rjy017 |
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