Evidence map›Paper›PMID 38715896›Full record

ArticleDEN open2025

Immunoglobulin G4 -related gastrointestinal disease associated with type 1 autoimmune pancreatitis: A case report.

Shingo Sato, Toyotaka Kasai, Hiroyuki Eto, Shikiko Okamoto, Ariki Nagashima, Rui Ushiyama, Reiri Shimazaki, Hiroshi Nitta, Motonori Arai, Hiroshi Ito

Abstract readCase Reports
In one paragraph

Article in DEN open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

10 authors.

Shingo SatoDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.ORCID https://orcid.org/0009-0009-3132-0158
Toyotaka KasaiDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.
Hiroyuki EtoDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.
Shikiko OkamotoDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.
Ariki NagashimaDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.
Rui UshiyamaDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.
Reiri ShimazakiDepartment of Surgery Fukaya Red Cross Hospital Saitama Japan.
Hiroshi NittaDepartment of Surgery Fukaya Red Cross Hospital Saitama Japan.
Motonori AraiDepartment of Diagnostic Pathology Fukaya Red Cross Hospital Saitama Japan.
Hiroshi ItoDepartment of Gastroenterology Fukaya Red Cross Hospital Saitama Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoglobulin G4 (IgG4)-related diseaseis a systemic inflammatory condition of unknown etiology characterized by increases in serum IgG4 and in the number of IgG4-positive cells in affected tissues. One of the commonly involved locations is the pancreas; this condition is known as type 1 autoimmune pancreatitis (AIP). Type 1 AIP, which shows a biliary stricture in the intrapancreatic bile duct, can be misdiagnosed as a malignancy due to similar cholangiography findings and clinical presentation. In rare cases complicated by post-bulbar duodenal ulcers, differentiating between type 1 AIP and malignancies is even more difficult. An 81-year-old male was referred to our hospital for the treatment of a pancreatic head mass and obstructive jaundice. Serological and radiological findings were consistent with both type 1 AIP and a malignancy. Gastroduodenoscopy revealed a post-bulbar duodenal ulcer with endoscopic features that evoked malignant duodenal invasion. Although biopsies were negative for malignant cells, subsequent bleeding from the lesion suggested the progression of malignancy, which led to surgical resection. Pancreatoduodenectomy and pathological examination indicated that type 1 AIP was present. Simultaneously, the involvement of IgG4-related disease in the ulcerative lesion was suggested. To our knowledge, this is the first reported case of type 1 AIP complicated by post-bulbar duodenal ulcers, which was misdiagnosed as malignancy and considered an IgG4-related gastrointestinal disease associated with type 1 AIP.

Indexed as

autoimmune pancreatitisduodenal ulcerendoscopygastrointestinal tractimmunoglobulin G4‐related disease

Identifiers

PMID38715896
PMCPMC11075072

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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.