Evidence map›Paper›PMID 41589167›Full record

ArticleCureus2025

Early Detection and Curative Endoscopic Submucosal Dissection of a 4-mm Signet Ring Cell Microcarcinoma in a Reconstructed Gastric Tube: A Case Report.

Masao Sato, So Takahashi, Masahide Shimura, Naohiro Kobayashi, Suguru Arata, Takahiro Domen, Misa Yamauchi, Katsunori Iijima

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

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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

8 authors.

Masao SatoDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
So TakahashiDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Masahide ShimuraDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Naohiro KobayashiDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Suguru ArataDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Takahiro DomenDepartment of Gastroenterology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Misa YamauchiDepartment of Pathology, Yuri Kumiai General Hospital, Yurihonjo, JPN.
Katsunori IijimaDepartment of Gastroenterology and Neurology, Akita University Graduate School of Medicine, Akita, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric tube cancers are rare but clinically challenging entities that may arise years after esophageal or gastric surgery. Due to anatomical alteration and subtle mucosal changes, early detection remains difficult, particularly for signet-ring cell carcinoma (SRCC), which often progresses unnoticed. We report a rare case of micro SRCC arising in a reconstructed gastric tube, which was detected early and curatively resected by endoscopic submucosal dissection (ESD). The patient was initially diagnosed with adenocarcinoma of the esophagogastric junction during a routine esophagogastroduodenoscopy (EGD) performed as part of a medical check-up at a local clinic. He underwent ESD, but the pathological evaluation revealed a positive vertical margin, and he was subsequently referred to a tertiary center. Curative resection was achieved through open proximal gastrectomy combined with robot-assisted thoracoscopic esophagectomy of the middle and lower esophagus. Two years postoperatively, a follow-up EGD revealed a small, flat, whitish lesion measuring 5 mm on the lesser curvature of the gastric angle in the reconstructed gastric tube. Biopsy results revealed undifferentiated-type gastric cancer, predominantly composed of SRCC. Given the lesion's clearly shallow invasion and very small size on endoscopic examination, ESD was performed. Pathological findings confirmed a 4 × 4 mm SRCC limited to the mucosal layer, with negative horizontal and vertical margins, and no lymphovascular invasion, consistent with curative resection. This case highlights the importance of vigilant long-term endoscopic follow-up after upper gastrointestinal surgery and demonstrates that even micro SRCCs in reconstructed gastric tubes can be successfully detected and treated at an early stage by ESD.

Indexed as

egdendoscopic submucosal dissectionesdesophagogastroduodenoscopygastric cancergastric tubegastric tube cancerreconstructive gastric tubesignet-ring cell carcinomaundifferentiated gastric cancer

Identifiers

PMID41589167
PMCPMC12831960

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