Evidence map›Paper›PMID 35475041›Full record

ArticleCureus2022

A Rare Case of Juvenile Polyposis Syndrome Mimicking Ménétrier's Disease.

Michelle Bernshteyn, Abdul Q Bhutta, Jozsef Bordas, Rohin Mehta, Muhammad Osman Arif

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

5 authors at 2 institutions in 1 country.

Michelle BernshteynInternal Medicine, Upstate University Hospital, Syracuse, USA.
Abdul Q BhuttaGastroenterology, Upstate University Hospital, Syracuse, USA.
Jozsef BordasPathology, Upstate University Hospital, Syracuse, USA.
Rohin MehtaPathology, Upstate University Hospital, Syracuse, USA.
Muhammad Osman ArifGastroenterology, Upstate University Hospital, Syracuse, USA.
SUNY Upstate Medical University · USUpstate University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a wide differential diagnosis within polyposis syndromes. Our case represents an interesting and diagnostically challenging diagnosis involving a 41-year-old male who presented with an incidental gastric mass on imaging and a colonic mass seen on colonoscopy. Following multiple endoscopic evaluations, histological analysis, and genetic testing, the patient was ultimately diagnosed with juvenile polyposis syndrome (JPS)/hereditary hemorrhagic telangiectasia (HHT) despite the initial suspicion for Ménétrier's disease. His disease course was complicated by an acute upper extremity thrombus and diagnosis of colorectal carcinoma. This case highlights the importance of a thorough evaluation when polyposis syndromes are suspected. Prompt and accurate diagnosis can aid in the treatment, surveillance, and prevention of colorectal carcinoma.

Indexed as

colonoscopycolorectal cancergastroenterology and endoscopygastrointestinal polyposisgi polyposis syndromejuvenile polyposis syndromemenetrier's diseasepolyposisprotein-losing enteropathyupper extremity deep venous thrombosis

Identifiers

PMID35475041
PMCPMC9022607
OpenAlexW4220917126

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.