Evidence map›Paper›PMID 36359508›Full record

ArticleDiagnostics (Basel, Switzerland)2022

Endoscopic Features of Gastric Epithelial Neoplasm of Fundic Gland Mucosa Lineage.

Kohei Matsumoto, Hiroya Ueyama, Takashi Yao, Tomoyo Iwano, Momoko Yamamoto, Hisanori Utsunomiya, Ryota Uchida, Daiki Abe, Shotaro Oki, Nobuyuki Suzuki and 8 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Clinicopathological characterization of extremely low-grade fundic gland tumors: a study of 11 of a variant of oxyntic gland adenomas.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
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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

18 authors.

Kohei MatsumotoDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Hiroya UeyamaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0002-5370-1009
Takashi YaoDepartment of Human Pathology, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0003-2287-7658
Tomoyo IwanoDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Momoko YamamotoDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Hisanori UtsunomiyaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Ryota UchidaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Daiki AbeDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Shotaro OkiDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0002-2517-8353
Nobuyuki SuzukiDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Atsushi IkedaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Noboru YatagaiDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Yoichi AkazawaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Tsutomu TakedaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Kumiko UedaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Daisuke AsaokaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Mariko HojoDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0001-9671-5585
Akihito NagaharaDepartment of Gastroenterology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.ORCID 0000-0001-5979-4384

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endoscopic features of gastric epithelial neoplasms of fundic gland mucosa lineage (GEN-FGML) have not been well investigated. We aimed to clarify the endoscopic features of GEN-FGML and differences between gastric adenocarcinoma of the fundic gland type (GA-FG) and fundic gland mucosa type (GA-FGM). A total of 62 GEN-FGML lesions, including 52 GA-FG and 10 GA-FGM, were retrospectively analyzed using endoscopic and clinicopathological findings to provide information of diagnostic value using white light imaging (WLI) and magnifying endoscopy with narrow-band imaging (M-NBI). GA-FG frequently presented with a whitish, submucosal tumor (SMT) shape with dilated vessels with branching architecture and background mucosa without atrophic change in WLI, an indistinct demarcation line (DL), dilatation of the crypt opening and intervening part (IP), and microvessels without distinct irregularity in M-NBI. GA-FGM frequently presented as a reddish, elevated lesion in WLI, with a distinct DL, dilatation of the IP, and an irregular microvascular pattern in M-NBI. As for an M-NBI diagnosis, five GA-FGM lesions met the diagnostic criteria for cancer, whereas none of the GA-FG lesions met the same criteria. We highlight the endoscopic features of GEN-FGML, and the differentiation between GA-FG and GA-FGM might be possible by combination of lesion color and morphology in WLI and M-NBI diagnoses.

Indexed as

gastric adenocarcinoma of fundic gland mucosa typegastric adenocarcinoma of fundic gland typegastric epithelial neoplasm of fundic gland mucosa lineagenarrow-band imagingoxyntic gland adenoma

Identifiers

PMID36359508
PMCPMC9689643

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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.