Log in to save to my catalogue

Jejunal gastrointestinal stromal tumor that developed in a patient with neurofibromatosis type 1: a...

Jejunal gastrointestinal stromal tumor that developed in a patient with neurofibromatosis type 1: a...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9079a1b14dff4c70ae2826a2dfc6b9c7

Jejunal gastrointestinal stromal tumor that developed in a patient with neurofibromatosis type 1: a case report

About this item

Full title

Jejunal gastrointestinal stromal tumor that developed in a patient with neurofibromatosis type 1: a case report

Publisher

London: BioMed Central Ltd

Journal title

Diagnostic pathology, 2023-10, Vol.18 (1), p.1-8, Article 110

Language

English

Formats

Publication information

Publisher

London: BioMed Central Ltd

More information

Scope and Contents

Contents

Background Neurofibromatosis type 1 (NF1) is known to be associated with the frequent occurrence of unique gastrointestinal stromal tumors (GISTs), preferably occurring in the small intestine, with no mutations in the c-kit proto-oncogene or platelet-derived growth factor receptor-alpha (PDGFRA), with a high tendency for multifocal development, ind...

Alternative Titles

Full title

Jejunal gastrointestinal stromal tumor that developed in a patient with neurofibromatosis type 1: a case report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_9079a1b14dff4c70ae2826a2dfc6b9c7

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_9079a1b14dff4c70ae2826a2dfc6b9c7

Other Identifiers

ISSN

1746-1596

E-ISSN

1746-1596

DOI

10.1186/s13000-023-01398-6

How to access this item