Evidence map›Paper›PMID 41030443›Full record

ArticleFrontiers in immunology2025

Case Report: An unexpected case of tumor regression in blue nevus melanoma following COVID-19 infection.

Yadriel Bracero, Emily Nghiem, Ajay K Singh, Divya B Kenchappa, Rachel Berglas, Shabnam Fidvi, Chaoyuan Kuang, Katia Papalezova, Beth McLellan, Bijal Amin and 1 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 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

11 authors.

Yadriel Bracero *Department of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Emily Nghiem *Department of Surgery, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY, United States.
Ajay K SinghDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Divya B KenchappaDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Rachel BerglasDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Shabnam FidviDepartment of Radiology, Albert Einstein College of Medicine, Bronx, NY, United States.
Chaoyuan KuangDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Katia PapalezovaDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.
Beth McLellanDepartment of Dermatology, Albert Einstein College of Medicine, Bronx, NY, United States.
Bijal AminDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, United States.
Yvonne M SaengerDepartment of Oncology, Albert Einstein College of Medicine, Bronx, NY, United States.

Funding

Applying pathomics to establish a biosignature for aggressive skin melanoma.R01CA260375 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rui Chang, Yvonne Margaret Saenger · 2021 to 2026
$3.1M
NCI NIH HHS R01 CA260375
6 · The paper itself

Abstract

Blue nevus is a benign melanocytic lesion that appears as a blue or dark mole due to the presence of melanin deep within the skin. In rare cases melanoma can arise from this association with blue nevus, and entity termed blue nevus melanoma (BNM). BNM most frequently occurs on the scalp and is an aggressive subtype of melanoma which has the tendency to metastasize. Similar to acral melanoma, BNM has a distinct genetic profile, is less linked to sun exposure, and has an equal incidence in patients of European and non-European ancestry. It is also less responsive to immunotherapy. This case report describes a diagnosis of blue nevus-related scalp melanoma characterized by GNA11 mutation in a 50-year-old female Hispanic patient, with a tumor refractory to multiple courses of combination immunotherapy who developed metastases to the liver and underwent microwave ablation of the hepatic lesions. Her disease course was complicated by hospitalization for infection with coronavirus disease of 2019 (COVID-19) and autoimmune hepatitis. Months after being discharged, surveillance imaging revealed a decrease in size of the existing lesions without additional therapeutic intervention. While this unusual response can be attributed to multiple factors, this observation aligns with emerging reports suggesting potential tumor remission associated with COVID-19 infection.

Indexed as

COVID-19MelanomaNevus, BlueSkin NeoplasmsFemaleHumansMiddle AgedSARS-CoV-2blue nevus melanomacase reportCOVID-19GNA11 mutationimmune checkpoint inhibitors (ICIs)immunotherapytumor regression

Identifiers

PMID41030443
PMCPMC12477163

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