Evidence map›Paper›PMID 33613165›Full record

ArticleCase reports in gastroenterology

Next-Generation Sequencing for Non-Ampullary Duodenal Carcinoma Suggesting the Existence of an Adenoma-Carcinoma Sequence.

Tsubasa Yoshida, Yohei Kojima, Ryusuke Shimada, Hidesato Tanabe, Koichi Tabei, Osamu Yanagida, Takashi Nikaido, Kouki Ohtsuka, Hiroaki Ohnishi, Nobutsugu Abe and 2 more

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In one paragraph

Article in Case reports in gastroenterology. 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

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, 0 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

12 authors at 2 institutions in 1 country.

Tsubasa YoshidaDepartment of Internal Medicine, Kosei Hospital, Tokyo, Japan.
Yohei KojimaDepartment of Surgery, Kosei Hospital, Tokyo, Japan.
Ryusuke ShimadaDepartment of Internal Medicine, Kosei Hospital, Tokyo, Japan.
Hidesato TanabeDepartment of Internal Medicine, Kosei Hospital, Tokyo, Japan.
Koichi TabeiDepartment of Internal Medicine, Kosei Hospital, Tokyo, Japan.
Osamu YanagidaDepartment of Surgery, Kosei Hospital, Tokyo, Japan.
Takashi NikaidoDepartment of Pathology, Kosei Hospital, Tokyo, Japan.
Kouki OhtsukaDepartment of Laboratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Hiroaki OhnishiDepartment of Laboratory Medicine, Kyorin University School of Medicine, Tokyo, Japan.
Nobutsugu AbeDepartment of Gastroenterological and General Surgery, Kyorin University School of Medicine, Tokyo, Japan.
Tadakazu HisamatsuDepartment of Gastroenterology and Hepatology, Kyorin University School of Medicine, Tokyo, Japan.
Shinichi TakahashiDepartment of Internal Medicine, Kosei Hospital, Tokyo, Japan.
Anjo Kosei Hospital · JPKyorin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duodenal tumors with a sporadic adenoma-carcinoma sequence are extremely rare. For such clinically suspected cases without a specific family history, performing a comprehensive gene search is important to understand the germline mutation background. We present a 68-year-old woman without a genetic or familial history of familial adenomatous polyposis (FAP), Peutz-Jeghers syndrome, or Lynch syndrome who presented to Kosei Hospital, Japan, with exertional dyspnea induced by abdominal pain lasting 3 weeks. A duodenal tumor was suspected by contrast-enhanced computed tomography. Esophagogastroduodenoscopy showed a lesion accompanied by a white microprotuberance on the descending part of the duodenum opposite the papilla, with a giant ulcerative lesion at the center of the white lesion. Biopsy revealed a low-grade adenoma, high-grade adenoma, and adenocarcinoma. Immunohistochemical analysis of the adenoma and adenocarcinoma showed Ki-67, p53, cytokeratin 20, caudal-type homeobox 2, and carcinoembryonic antigen positivity and cytokeratin 7 negativity. The findings suggested the presence of an adenoma-adenocarcinoma sequence in duodenal carcinoma. However, in the mutational analysis using next-generation sequencing, c.4348C>T (p.Arg1450Ter) mutation in APC was detected in all normal mucosal, adenoma, and carcinoma tissues. This mutation is common in FAP patients. Even if the presence of an adenoma-adenocarcinoma sequence in duodenal carcinoma is suggested in cases without a familial FAP history, as in this case, genetic analysis may reveal FAP. Thus, performing a comprehensive genetic analysis of duodenal carcinoma patients with a possible adenoma-carcinoma sequence is necessary to explore their genetic background.

Indexed as

Adenoma-carcinoma sequenceDuodenal cancerFamilial adenomatous polyposisNext-generation sequencing

Identifiers

PMID33613165
PMCPMC7879259
OpenAlexW3126057356

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