ArticleCureus2025
Focal Pigmented Squamous Cell Carcinoma (pSCC) In Situ of the Nail: A Rare Case Emphasizing Diagnostic Vigilance.
Article in Cureus, 2025. 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.
- Nail Squamous Cell Carcinoma Involving the Nail Fold in a Skin of Color Patient: A Case Report.Case reports in dermatologyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pigmented squamous cell carcinoma (pSCC) of the nail unit is an uncommon condition that can mimic benign entities. Clinically, pSCC can present as longitudinal melanonychia, onycholysis, or verrucous plaques, potentially leading to diagnostic delays. The pigmented variant is particularly challenging to diagnose, as it may be mistaken for benign melanocytic lesions. Histologically, pSCC demonstrates atypical keratinocyte proliferation with pigmentation, and immunohistochemical analysis is crucial to exclude melanocytic involvement. This case report describes a 25-year-old immunocompetent female with Fitzpatrick type IV skin who presented with progressive nail discoloration and sensitivity of the right thumb, persisting for approximately one year. Despite the absence of a personal or family history of skin malignancy, clinical evaluation and subsequent biopsy revealed focal pSCC in situ with wart-like histopathological features, including full-thickness epithelial atypia, papillomatosis, hypergranulosis, and keratohyalin granule formation. The patient was referred to Moh's micrographic surgery. This case underscores the importance of maintaining a broad differential diagnosis when evaluating persistent or evolving nail pigmentation, especially in patients without classic risk factors. The wart-associated histological changes suggest a possible link to human papillomavirus (HPV) infection, warranting further investigation into viral oncogenesis in nail unit SCC. Clinicians should maintain a high index of suspicion for atypical presentations, particularly in cases with progressive changes and associated pain, to ensure timely diagnosis and optimal management.
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