Evidence map›Paper›PMID 41937196›Full record

ArticleJournal of medical case reports2026

Amyloidosis with predominant gastrointestinal symptoms: a challenge for physicians and a burden for patients: a case report.

Masoud Faghieh Dinavari, Kasra Khodadadi, Amir-Taher Eftekhar-Sadat

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2026. 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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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

3 authors.

Masoud Faghieh DinavariLiver and Gastrointestinal Diseases Research Center, Emam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.
Kasra KhodadadiLiver and Gastrointestinal Diseases Research Center, Emam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran. khodadadikasra2020@gmail.com.
Amir-Taher Eftekhar-SadatDepartment of Pathology, Emam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGastrointestinal symptoms resulting from amyloid deposition can differ significantly and might be mistaken for other prevalent intestinal disorders, complicating the diagnostic process. Here, we present a case of systemic amyloidosis with gastrointestinal involvement, where the primary symptom of the disease is gastrointestinal issues. CASE PRESENTATION: A 63-year-old Iranian man presented with intermittent diarrhea, diffuse abdominal pain, and fatigue. The muscle strength of the lower limbs was 2/5, whereas that of the upper limbs was 4/5. Cardiac consultation was requested owing to electrocardiogram changes that were compatible with infiltrative cardiomyopathy. Esophagogastroduodenoscopy revealed multiple clean-based ulcers in the antrum. Four-limb electromyography and nerve conduction velocity was performed, leading to a diagnosis of chronic, partially active axonal-dominant type polyradiculoneuropathy. Owing to the involvement of various organs, particularly the heart, peripheral nervous system, and kidneys, we performed a biopsy of the abdominal fat pad owing to suspected amyloidosis.

conclusionAmyloidosis is a disease with many different manifestations. Although it may not be common, it can present a diagnostic challenge for clinicians, especially when gastrointestinal symptoms are pronounced.

Indexed as

AmyloidosisStomach UlcerAbdominal PainBiopsyDiarrheaElectromyographyEndoscopy, Digestive SystemFatigueHumansMaleMiddle AgedAmyloidosisBiopsyCase reportGastric ulcer

Identifiers

PMID41937196
PMCPMC13188414

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