ArticleCureus2026
Histologic Features of Melanocytic Nevi Secondary to Melanoma Treatment With Immune Checkpoint Inhibitors.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Halo Nevus as a Self-Limited Model of Melanocyte Autoimmunity: Bridging Vitiligo, Immune Resolution, and Tumor Immunology-A Narrative Review.Dermatopathology (Basel, Switzerland) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Programmed death-1 (PD-1) inhibitors are anticancer drugs that function as immune checkpoint blockers, targeting PD-1 proteins on the surface of cells to restore immune system activity against tumors. While cutaneous adverse events associated with immune checkpoint inhibitor therapy are well documented, this case highlights the reactive histopathologic changes that can occur in benign nevi during treatment. Here, we present the case of a 51-year-old Hispanic female with a history of melanoma on the chest who was seen in clinic for routine follow-up. Three suspicious pigmented lesions located on the right upper back, abdomen, and left shoulder were biopsied for further analysis. Histopathologic examination indicated an intradermal melanocytic nevus with irritation and inflammation, an inflamed, mildly dysplastic compound melanocytic nevus, and a compound melanocytic nevus with marked inflammation and no atypia. Additional clinical history revealed that the patient was receiving treatment for advanced melanoma with immune checkpoint inhibitors. Increased awareness of these features in melanocytic lesions associated with PD-1 and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors may help with accurate diagnosis.
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Registered trials
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