Evidence map›Paper›PMID 41835964›Full record

ArticleClinical, cosmetic and investigational dermatology2026

Muir-Torre Syndrome: A Rare Case Report and Review of Literature.

Zihao Chen, Yan Wan, Chen Zhou, Luying Wang, Ran Huo

Abstract readCase Reports
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2026. 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
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.

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

5 authors.

Zihao ChenDepartment of Burn and Plastic Surgery, Shandong Provincial Hospital, Shandong University, Jinan, People's Republic of China.ORCID 0009-0004-9217-7977
Yan WanDepartment of Burn and Plastic Surgery, Shandong Provincial Hospital, Shandong University, Jinan, People's Republic of China.
Chen ZhouDepartment of Burn and Plastic Surgery, Shandong Provincial Hospital, Shandong University, Jinan, People's Republic of China.
Luying WangDepartment of Burn and Plastic Surgery, Shandong Provincial Hospital, Shandong University, Jinan, People's Republic of China.
Ran HuoDepartment of Burn and Plastic Surgery, Shandong Provincial Hospital, Shandong University, Jinan, People's Republic of China.ORCID 0000-0002-3513-1073

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muir-Torre syndrome (MTS) is an uncommon autosomal dominant disorder characterized by germline mutations in DNA mismatch repair (MMR) genes, resulting in microsatellite instability (MSI). It is regarded as a variant form of Lynch syndrome, characterized by the co-occurrence of at least one cutaneous sebaceous neoplasm and at least one visceral malignancy. Furthermore, studies have indicated that MTS may manifest in transplant recipients and in immunocompromised patients. The diagnosis and management of such cases necessitate a multidisciplinary approach. Here, we report a case of a Chinese patient with a history of rectal cancer who developed multiple sebaceous adenomas during immunosuppressive therapy six years after renal transplantation. This case report not only provides additional evidence for the inducing effect of immunosuppressants on MTS but also emphasizes the importance of a thorough diagnosis of MTS and the significance of preventing the development of potential skin tumors in patients with MTS.

Indexed as

cutaneous sebaceous neoplasmDNA mismatch repairimmunosuppressive therapymuir-torre syndrome

Identifiers

PMID41835964
PMCPMC12988781

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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.