Evidence map›Paper›PMID 36540528›Full record

ArticleCureus2022

Familial Adenomatous Polyposis: Case Report and Literature Review.

Juan José Chaves, Viviana Chaves-Cabezas, Rafael Parra-Medina, José Octavio Chaves-Chamorro

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 50% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Juan José ChavesDepartment of Pathology, Fundación Universitaria de Ciencias de la Salud, Hospital San José, Bogota, COL.
Viviana Chaves-CabezasDepartment of Pathology, Fundación Universitaria de Ciencias de la Salud, Hospital San José, Bogotá, COL.
Rafael Parra-MedinaDepartment of Pathology, Fundación Universitaria de Ciencias de la Salud, Hospital San José, Bogotá, COL.
José Octavio Chaves-ChamorroDepartment of Gastroenterology, Hospital Civil de Ipiales, Ipiales, COL.
Fundación Universitaria de Ciencias de la Salud · COHospital de Especialidades · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial adenomatous polyposis (FAP) is an autosomal inheritance disease characterized by 100 or more adenomatous polyps in the colon and rectum with a high risk of developing colorectal carcinoma (CRC). The management of this disease is based on early screening and timely follow up, with subsequent planning of risk-reducing or therapeutic surgeries. We present a case of a patient with a strong family history of FAP with a "de novo" diagnosis of CRC. Furthermore, a literature discussion of current and future perspectives of treatment is performed.

Indexed as

colombiacolorectal cancerfamilial adenomatous polyposisfamily researchgenetic syndromes

Identifiers

PMID36540528
PMCPMC9759120
OpenAlexW4309183679

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.