Evidence map›Paper›PMID 39460489›Full record

ArticleThe Journal of dermatology2024

First reported case of thymoma-associated multiorgan autoimmunity induced by COVID-19.

Rie Hyobu, Miho Mori, Tatsuo Maeda, Kazuki Fujimori, Yukako Shimai, Makiko Naito, Masayuki Masuda, Tatsuo Ohira, Norihiko Ikeda, Yukari Okubo and 1 more

Abstract readCase Reports
In one paragraph

Article in The Journal of dermatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Rie HyobuDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.ORCID https://orcid.org/0009-0008-1960-3326
Miho MoriDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.
Tatsuo MaedaDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.
Kazuki FujimoriDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.
Yukako ShimaiDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.
Makiko NaitoDepartment of Neurology, Tokyo Medical University, Tokyo, Japan.
Masayuki MasudaDepartment of Neurology, Tokyo Medical University, Tokyo, Japan.
Tatsuo OhiraDepartment of Surgery, Tokyo Medical University, Tokyo, Japan.
Norihiko IkedaDepartment of Surgery, Tokyo Medical University, Tokyo, Japan.
Yukari OkuboDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9526-1259
Kazutoshi HaradaDepartment of Dermatology, Tokyo Medical University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9059-4097

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymoma-associated multiorgan autoimmunity (TAMA) presents with skin symptoms similar to those of graft-versus-host disease (GVHD), liver dysfunction, and enteritis, in the absence of a history of hematopoietic stem cell or bone marrow transplantation. TAMA is a type of paraneoplastic syndrome associated with thymoma. Its etiology is unclear but is thought to be a result of breakdown of immune tolerance. Histopathologically, TAMA is characterized by epidermal acanthosis with parakeratosis, individual cell keratinization, liquefaction degeneration, and intraepidermal infiltration of CD8-positive lymphocytes. A 64-year-old female patient with a history of myasthenia gravis and thymoma treated with prednisolone (10 mg/day) and cyclosporine (150 mg/day) experienced erythema on her trunk after coronavirus disease 2019 (COVID-19) onset. A psoriatic drug eruption was suspected and the possible causative drug was discontinued, but the skin rash failed to improve. A skin biopsy demonstrated GVHD-like histopathological findings. Diarrhea, abdominal pain, and duodenal perforation occurred concurrently, leading to the diagnosis of TAMA. Thereafter, the patient continued prednisolone and cyclosporine in the same doses as the TAMA treatment and added topical steroids. During the disease course, candida fungemia and cytomegalovirus infection developed, resulting in the patient's death. The TAMA was considered to have been caused by the release of inflammatory cytokines, autoreactive T cell activation, and regulatory T cell dysfunction induced by COVID-19.

Indexed as

COVID-19ThymomaThymus NeoplasmsAutoimmune DiseasesAutoimmunityBiopsyCyclosporineFatal OutcomeFemaleHumansMiddle AgedParaneoplastic SyndromesPrednisoloneSARS-CoV-2SkinCyclosporinePrednisolonealopeciaCOVID‐19graft‐versus‐host diseasemyasthenia gravisthymoma

Identifiers

PMID39460489
PMCPMC11624154

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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.