Evidence map›Paper›PMID 26649731›Full record

ArticleVirchows Archiv : an international journal of pathology2016

Syndromic versus non-syndromic sporadic gastrin-producing neuroendocrine tumors of the duodenum: comparison of pathological features and biological behavior.

M Johannes Rosentraeger, Nele Garbrecht, Martin Anlauf, Andreas Raffel, Wolfram T Knoefel, Bertram Wiedenmann, Günter Klöppel

Abstract readComparative Study
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Concept of neuroendocrine neoplasms of all organs with a focus on grading, subtyping.Virchows Archiv : an international journal of pathology · 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

7 authors.

M Johannes RosentraegerFirst Department of Medicine, University Hospital Schleswig-Holstein, Christian-Albrechts University, Arnold-Heller-Str. 3, Kiel, 24105, Germany. johannes.rosentraeger@uksh.de.ORCID http://orcid.org/0000-0001-5893-1033
Nele GarbrechtDepartment of Pathology, University Hospital Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany.
Martin AnlaufInstitute of Pathology and Cytology, St. Vincenz Hospital, Limburg, Germany.
Andreas RaffelDepartment of General, Visceral and Pediatric Surgery, University Hospital of Düsseldorf, Düsseldorf, Germany.
Wolfram T KnoefelDepartment of General, Visceral and Pediatric Surgery, University Hospital of Düsseldorf, Düsseldorf, Germany.
Bertram WiedenmannDepartment of Hepatology and Gastroenterology, Charité, Campus Virchow Clinic, Berlin, Germany.
Günter KlöppelDepartment of Pathology, Consultation Center for Pancreatic and Endocrine Tumors, Technical University, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sporadic gastrin-producing neuroendocrine tumors of the duodenum present either with the Zollinger-Ellison syndrome (ZES) or with unspecific symptoms. While syndromic gastrin-producing neuroendocrine tumors often show metastases at the time of diagnosis, those without a syndrome do not. The aim of the study was to search for clinicopathological features that may distinguish the two categories of gastrin-producing duodenal tumors. In a retrospective study, we analyzed the clinical and pathological data in a series of 41 patients with syndromic (i.e., gastrinomas) or non-syndromic duodenal gastrin-producing neuroendocrine tumors (ns-gas-NETs). Twenty-four (59 %) of the 41 patients had tumors that were associated with a ZES and were classified as gastrinomas. These tumors showed a higher Ki-67 index than that of the ns-gas-NETs (1.74 vs. 0.85 %, p = 0.012). In addition, they had more lymph node metastases (75 vs. 6 %, p < 0.001) and showed liver metastases and thus presented much more frequently in TNM stage ≥III (75 vs. 6 %; p < 0.001) than their non-syndromic counterparts. Gastrinomas were removed surgically, ns-gas-NETs endoscopically. We did not observe any significant differences in overall survival or recurrence of disease. Duodenal gastrinomas show no clear morphological features that distinguish them from their non-syndromic counterparts. However, the patients with gastrinomas present in a more advanced stage of disease and need surgical treatment, while non-syndromic gastrin-producing duodenal NETs may be cured by complete endoscopical removal.

Indexed as

AdultAgedAged, 80 and overDuodenal NeoplasmsFemaleGastrinomaGastrinsHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeuroendocrine TumorsPancreatic NeoplasmsRetrospective StudiesGastrinsDuodenumGastrinomaGastrin productionNeuroendocrine tumorsZollinger-Ellison syndrome

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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.