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Article

Multiple gastrointestinal stromal tumors: Clinicopathologic and genetic analysis of 12 patients.

The American journal of surgical pathology - 1 Feb 2007

Kang Dae Young, Park Cheol Keun, Choi Jong Sang, Jin So Young, Kim Hyun Jung, Joo Mee, Kang Mi Seon, Moon Woo Sung, Yun Ki Jung, Yu Eun Sil, Kang Haeyun, Kim Kyoung-Mee

Abstract excerpt

Multiple gastrointestinal stromal tumors (GISTs) are extremely rare and usually associated with type 1 neurofibromatosis and familial GIST. The aim of this study was to investigate the clinical, phenotypic, and genetic characteristics of multiple GISTs to gain insights into their underlying pathogenesis and clinical behavior. Forty-seven paraffin blocks of multiple GISTs from 12 patients were analyzed. Genomic...

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Share to DNA, Neoplasm
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Germ-Line Mutation

Share to Intestinal Mucosa

Share to Neoplasms, Multiple Primary

Share to Neurofibromatosis 1

Share to Proto-Oncogene Proteins c-kit

Share to Receptor, Platelet-Derived Growth Factor alpha

Source

Identifiers

PMID: 17255767
DOI: 10.1097/01.pas.0000213318.66800.94

Genes

KIT
PDGFRA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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