Evidence map›Paper›PMID 41122652›Full record

ArticleFrontiers in oncology2025

Case Report: Surgery combined with targeted therapy for metastatic anorectal malignant mucosal melanoma.

Yadong Yao, Pule Liu, Kai Liu, Lirong Lian, Shuo Gao

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2025. 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.

Yadong YaoDepartment of General Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, China.
Pule LiuDepartment of General Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, China.
Kai LiuThe Second Clinical Medical College of Lanzhou University, Lanzhou, Gansu, China.
Lirong LianDepartment of General Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, China.
Shuo GaoDepartment of General Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Anorectal mucosal melanoma is a rare tumor with a poor prognosis. Timely diagnosis and treatment are essential for improving patient survival. Currently, there is no standardized treatment approach for this disease. This case report emphasizes the effectiveness of combining surgery with targeted therapy for advanced KIT-mutated anorectal mucosal melanoma, as well as the potential adverse effects during targeted therapy. Case report: We report a 66-year-old female diagnosed with primary anorectal mucosal melanoma with liver metastasis. She underwent a transanal local excision to remove the primary anorectal mucosal melanoma and ultrasound-guided radiofrequency ablation for the liver metastasis. After surgery, she received targeted therapy with imatinib due to the presence of c-Kit mutations. The results showed the expected clinical efficacy. Unfortunately, the patient later developed portal vein thrombosis and liver dysfunction during the imatinib therapy, necessitating the discontinuation of targeted therapy. Conclusions: The combination of transanal local excision of the primary lesion and radiofrequency ablation of liver metastases, complemented by imatinib-targeted therapy, represents a feasible therapeutic strategy for advanced KIT-mutated anorectal mucosal melanoma. This strategy may prolong patient survival; however, potential adverse events require careful monitoring.

Indexed as

anorectal mucosal melanomaKIT mutationprognosissurgerytargeted therapy

Identifiers

PMID41122652
PMCPMC12535906

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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.