Evidence map›Paper›PMID 36998347›Full record

ArticleDEN open2023

Endoscopic resection for a solitary Peutz-Jeghers type polyp in the duodenum: A case report with literature review.

Yasuhiko Hamada, Masaki Katsurahara, Yuhei Umeda, Yohei Ikenoyama, Akina Shigefuku, Yasuko Fujiwara, Tuyoshi Beppu, Junya Tsuboi, Reiko Yamada, Misaki Nakamura and 3 more

Open access · goldFull text readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in DEN open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

13 authors at 1 institution in 1 country.

Yasuhiko HamadaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.ORCID https://orcid.org/0000-0001-5564-184X
Masaki KatsuraharaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Yuhei UmedaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Yohei IkenoyamaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Akina ShigefukuDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Yasuko FujiwaraDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Tuyoshi BeppuDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Junya TsuboiDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Reiko YamadaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Misaki NakamuraDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Kyosuke TanakaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Noriyuki HorikiDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Hayato NakagawaDepartment of Gastroenterology and Hepatology Mie University Hospital Tsu Mie Japan.
Mie University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 68-year-old female patient was referred to our hospital with a 30-mm polyp in the second portion of the duodenum found via esophagogastroduodenoscopy. The polyp had an irregular, lobular surface and a thick stalk. In addition, white dots were detected on the surface. Magnifying endoscopy with narrow-band imaging showed a white material deep in the loop-shaped microvessels on the white dots. Endoscopic ultrasonography showed a hypoechoic elevated lesion from the mucosal layer, and a feeding vessel traversing the stalk to supply the head of the polyp. Endoscopic biopsy did not provide a definitive diagnosis. Endoscopic resection was conducted for a definitive diagnosis and treatment. The resected specimen showed a branching bundle of smooth muscle fibers covered by hyperplastic mucosa, consistent with a hamartomatous polyp. The patient had no mucocutaneous pigmentation or familial history of the hamartomatous polyp. The polyp was finally diagnosed as a solitary Peutz-Jeghers-type polyp. No recurrence has been observed for seven years postoperatively.

Indexed as

duodenumendoscopic resectionhamartomatous polypPeutz‐Jeghers syndromePeutz‐Jeghers‐type polyp

Identifiers

PMID36998347
PMCPMC10043356
OpenAlexW4361291432

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read11
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.