Evidence map›Paper›PMID 29222587›Full record

ArticleJournal of gastroenterology2018

Gastrointestinal manifestation of immunoglobulin G4-related disease: clarification through a multicenter survey.

Kenji Notohara, Terumi Kamisawa, Kazushige Uchida, Yoh Zen, Mitsuhiro Kawano, Satomi Kasashima, Yasuharu Sato, Masahiro Shiokawa, Takeshi Uehara, Hajime Yoshifuji and 11 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of gastroenterology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 1% of its field
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

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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

21 authors at 17 institutions in 1 country.

Kenji NotoharaDepartment of Anatomic Pathology, Kurashiki Central Hospital, Kurashiki, Japan.ORCID http://orcid.org/0000-0001-5618-1312
Terumi KamisawaDepartment of Internal Medicine, Tokyo Metropolitan Komagome Hospital, Tokyo, Japan. kamisawa@cick.jp.
Kazushige UchidaDepartment of Gastroenterology and Hepatology, Kansai Medical University, Hirakata, Osaka, Japan.
Yoh ZenDepartment of Diagnostic Pathology, Kobe University Graduate School of Medicine, Kobe, Japan.
Mitsuhiro KawanoDivision of Rheumatology, Department of Internal Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.
Satomi KasashimaDepartment of Pathology, National Hospital Organization, Kanazawa Medical Center, Kanazawa, Japan.
Yasuharu SatoDepartment of Pathology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Masahiro ShiokawaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Takeshi UeharaDepartment of Laboratory Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Hajime YoshifujiDepartment of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hiroko HayashiDepartment of Pathology, Nagasaki University Graduate School of Biomedical Science, Nagasaki, Japan.
Koichi InoueDivision of Surgery, Yamachika Memorial Hospital, Odawara, Kanagawa, Japan.
Keisuke IwasakiDepartment of Pathology, Sasebo City General Hospital, Sasebo, Japan.
Hiroo KawanoDepartment of Laboratory Science, Faculty of Health Science, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Hiroyuki MatsubayashiDivision of Endoscopy, Shizuoka Cancer Center, Suntogun, Shizuoka, Japan.
Yukitoshi MoritaniMoritani Surgical Clinic, Okayama, Japan.
Katsuhiko MurakawaDepartment of Surgery, Obihiro Kosei General Hospital, Obihiro, Japan.
Yoshio OkaDepartment of Surgery, Nishinomiya Municipal Central Hospital, Nishinomiya, Japan.
Masatoshi TatenoDepartment of Pathology, Kushiro Red Cross Hospital, Kushiro, Japan.
Kazuichi OkazakiDepartment of Gastroenterology and Hepatology, Kansai Medical University, Hirakata, Osaka, Japan.
Tsutomu ChibaDepartment of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kyoto University · JPKansai Medical University · JPKanazawa Medical Center · JPKanazawa University · JPKobe University · JPKurashiki Central Hospital · JPKushiro Rosai Hospital · JPNagasaki University · JPNishinomiya Municipal Central Hospital · JPObihiro Kosei General Hospital · JPOkayama Psychiatric Medical Center · JPOkayama University · JPSasebo City General Hospital · JPShinshu University · JPShizuoka Cancer Center · JPTokyo Metropolitan Komagome Hospital · JPYamaguchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral reports on immunoglobulin (Ig)G4-related disease (IgG4-RD) with gastrointestinal involvement (IgG4-related gastrointestinal disease; IgG4-GID) have been published, although this entity has not been fully established clinicopathologically. Thus, we carried out a multicenter survey.

methodsPatients with possible IgG4-GID who underwent resection were collected. Histologic slides were reevaluated, and eight cases with diffuse lymphoplasmacytic infiltration but without numerous neutrophils, granulations or epithelioid granulomas were further analyzed.

resultsOverall, the IgG4 counts (87-345/high-power field) and IgG4/IgG-positive ratio were high (44-115%). The demographic findings included advanced age among the patients (55-80 years) and male preponderance (six cases). Six lesions (five gastric, one esophageal), consisting of lymphoplasmacytic infiltration with neural involvement in the muscularis propria and/or bottom-heavy plasmacytosis in the gastric mucosa, were histologically regarded as highly suggestive of IgG4-RD. Storiform fibrosis and obliterative phlebitis were found in two cases, and the former gave rise to a 7-cm-sized inflammatory pseudotumor (IPT) in one case. Ulceration and carcinoma co-existed in three and two lesions, respectively. All the patients had other organ involvement (OOI), and serum IgG4 levels were markedly elevated (four of five patients). The remaining two cases with gastric IPTs featuring reactive nodular fibrous pseudotumor or nodular lymphoid hyperplasia were regarded as possible cases of IgG4-RD because of the histologic findings and lack of OOI.

conclusionsIgG4-GID is found in the setting of IgG4-RD, often with ulceration or cancer. Characteristic histologic findings are observed in the muscularis propria and gastric mucosa. Cases with IPT may be heterogeneous, and there may be mimickers of IgG4-GID.

Indexed as

AgedAged, 80 and overAge FactorsDiagnosis, DifferentialFemaleFibrosisFollow-Up StudiesGastrointestinal DiseasesGastrointestinal TractGranuloma, Plasma CellHumansImmunoglobulin GImmunoglobulin G4-Related DiseaseJapanMaleMiddle AgedImmunoglobulin GGastrointestinal tractIgG4IgG4-related diseaseInflammatory pseudotumorPathology

Identifiers

PMID29222587
OpenAlexW2771931581

What OpenQuestion holds

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Registered trials

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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.