ArticleInternational journal of clinical and experimental pathology2020
Multiple gastrointestinal stromal tumors with exon 11 mutation of the c-KIT gene in a young male without family history.
Article in International journal of clinical and experimental pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
- Chinese Pedigree with Hereditary Gastrointestinal Stromal Tumors: A Case Report and Literature Review.International journal of molecular sciences · 2023Review
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Multiple gastrointestinal stromal tumors (GISTs) are extremely rare, usually related to specific tumor syndromes such as familial GIST syndrome, neurofibromatosis type 1 (NF1), and the Carney triad. A 27-year-old man came to the hospital for treatment due to watery bloody stool. Abdominal CT disclosed multiple tumors in the gastrointestinal tract. The postoperative pathological examination showed multiple GISTs and diffuse hyperplasia of interstitial cells of Cajal. The c-KIT mutation at exon 11 c.1676T>C (p.V559A) was detected in the paraffin-embedded tumor tissue. He had skin hyperpigmentation from childhood, but had no family history of GIST. This case of multiple GISTs without family history attracted our attention.
Indexed as
Identifiers
32782703PMC7414506W3049412346What OpenQuestion holds
Registered trials
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