Evidence map›Paper›PMID 41695178›Full record

ArticleFrontiers in medicine2026

Case Report: Image-enhanced endoscopic characteristics of gastric amyloidosis with narrow-band imaging comparison.

Xueman Wang, Bo Lian, Quan Luo, Xintong Jiang, Jian Dong, Tiannu Ding, Qiaoying Zhang, Yan Tang, Lifeng Hu

Abstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Xueman WangEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Bo LianEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Quan LuoEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Xintong JiangEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Jian DongEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Tiannu DingEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Qiaoying ZhangForensic Center, Shaoxing University, Shaoxing, Zhejiang, China.
Yan TangEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.
Lifeng HuEndoscopy Center, Shaoxing People's Hospital (The First Affiliated Hospital, Shaoxing University), Shaoxing, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastrointestinal (GI) amyloidosis is a rare disorder with nonspecific clinical and endoscopic features, often leading to misdiagnosis. Timely recognition is crucial to prevent diagnostic delays and systemic complications. Case Presentation: A 64-year-old male initially presented with upper respiratory symptoms, and chest computed tomography (CT) performed for pneumonia evaluation incidentally revealed esophageal wall thickening. The first endoscopy showed diffuse redness with loss of the regular arrangement of collecting venules in the gastric body, and the findings were initially interpreted as Helicobacter pylori-associated gastritis. However, both gastric histopathology and the ¹³C urea breath test were negative, and no clear cause of erythema was identified. The patient's symptoms resolved after taking anti-inflammatory medication, and he did not return for follow-up as instructed. One year later, the patient developed proteinuria and bilateral lower extremity edema and was diagnosed with systemic light-chain (AL) amyloidosis involving the kidneys and heart. Repeat endoscopy revealed disc- and linear-shaped gastric erythema with a submucosal tumor (SMT)-like protrusion. Congo red staining with polarized light confirmed amyloid deposition in the gastric biopsy. In addition, we compared the endoscopic features of gastric erythema from three different etiologies. On narrow-band imaging (NBI), amyloid-related erythema showed a grayish-green signal with a more layered, deeper-appearing distribution, whereas vonoprazan-associated and Helicobacter pylori-associated erythema appeared more superficial with limited layering. Because absolute color intensity is not consistently comparable across panels, this observation should be considered hypothesis-generating rather than diagnostic. Conclusion: This case highlights the diverse and potentially misleading endoscopic manifestations of GI amyloidosis. NBI may aid in visualizing the distribution pattern and apparent depth of amyloid-related mucosal signals and serve as a supportive diagnostic tool; however, histological confirmation via Congo red staining remains the gold standard. The combination of image-enhanced endoscopy, targeted biopsies, and multidisciplinary evaluation may facilitate earlier recognition and more comprehensive management of patients with atypical gastric erythema.

Indexed as

Congo red stainingendoscopygastric erythemagastrointestinal amyloidosisHelicobacter pylorilight-chain amyloidosis (AL)

Identifiers

PMID41695178
PMCPMC12894309

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