ArticleInternational journal of clinical and experimental pathology2017
Stomach desmoid tumor: a case report and review of the literature.
Article in International journal of clinical and experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed, 5 citations in OpenAlex.
- Large desmoid tumour of the small bowel mesentery.BMJ case reports · 2022Article
- Gastric Desmoid Fibromatosis - Report of a Rare Mimic of Gastrointestinal Stromal Tumor.Cureus · 2021Article
- Calcifying fibrous tumor of the gastrointestinal tract: A clinicopathologic review and update.World journal of gastroenterology · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Desmoid tumors, also known as aggressive fibromatoses, are clinically rare soft-tissue tumors that arise from such connective tissues as the musculoaponeurotic structures. The majority of the reported intra-abdominal desmoid tumors occur in the small intestinal mesentery and peritoneum, whereas stomach desmoid tumors are extremely rare. The present study reports a case of stomach desmoid tumor and reviews the related available literature. The diagnosis of the stomach desmoid tumors can be made with routine pathological and immunohistochemical examinations. Compared with desmoid tumors at other sites, the currently preferred treatment of the stomach desmoid tumors with negative margins is radical resection of tumors. All the follow-ups of patients with the stomach desmoid tumors show no obvious recurrence, suggesting that the prognosis of the stomach desmoid tumors is good.
Indexed as
Identifiers
31966392PMC6965783W3026308673What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.