Evidence map›Paper›PMID 37899945›Full record

ArticleCase reports in dermatology

A Case of Lamina Lucida-Type Linear IgA Disease Complicated by Colon Polyposis and Rectal Adenocarcinoma.

Akiko Miyazaki, Saori Itoi-Ochi, Mami Hayashi, Asako Ota, Kengo Nagai, Shinya Inoue, Naohiro Tomita, Hidetaka Eguchi, Yasushi Okazaki, Hideyuki Ishida and 1 more

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In one paragraph

Article in Case reports in dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 67% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 5 institutions in 1 country.

Akiko MiyazakiDepartment of Dermatology, Suita Municipal Hospital, Osaka, Japan.
Saori Itoi-OchiDepartment of Dermatology, Suita Municipal Hospital, Osaka, Japan.
Mami HayashiDepartment of Dermatology, Suita Municipal Hospital, Osaka, Japan.
Asako OtaDepartment of Dermatology, Suita Municipal Hospital, Osaka, Japan.
Kengo NagaiDepartment of Gastroenterology, Suita Municipal Hospital, Osaka, Japan.
Shinya InoueDepartment of Hematology, Suita Municipal Hospital, Osaka, Japan.
Naohiro TomitaCancer Treatment Center, Toyonaka Municipal Hospital, Osaka, Japan.
Hidetaka EguchiDiagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Yasushi OkazakiDiagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Hideyuki IshidaDepartment of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, Saitama, Japan.
Takashi HashimotoDepartment of Dermatology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Suita Municipal Hospital · JPJuntendo University · JPOsaka Metropolitan UniversitySocial Insurance Saitama Chuo Hospital · JPToyonaka Municipal Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linear IgA disease (LAD) is a rare autoimmune bullous disease characterized by IgA deposition in the basement membrane zone (BMZ). A 66-year-old male was treated for myelodysplastic syndrome at our hospital for 5 years, during which his condition remained stable. He visited our department because of erythema with itching, which appeared 1 year ago and gradually exacerbated with the development of blisters and erosions. During the first visit, multiple erythemas with erosions and crusts on their periphery were observed on the trunk and lower limbs. Histopathological examination revealed subepidermal blisters with inflammatory cell infiltration, mainly constituting of neutrophils, eosinophils, and lymphocytes. Direct and indirect immunofluorescence showed linear IgA deposits in the BMZ and IgA anti-BMZ antibodies, respectively, while immunoblotting using a concentrated culture supernatant of HaCaT cells detected IgA antibodies reactive to 120-kDa LAD-1. Accordingly, the patient was diagnosed with lamina lucida-type LAD. Subsequent colonoscopy revealed multiple colorectal polyps and rectal adenocarcinoma (Tis, N0, and M0). Multigene panel test showed an

Indexed as

Colorectal carcinomaDiaphenylsulfoneLinear IgA diseaseMultiple colorectal polypsMyelodysplasia syndrome

Identifiers

PMID37899945
PMCPMC10601694
OpenAlexW4387543226

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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.