ArticleClinical case reports2026
Palatal Congenital Melanocytic Nevus With Unusual Clinical Feature: A Rare Case Report With Literature Review.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital melanocytic nevi are uncommon benign lesions that primarily involve the skin and are exceedingly rare within the oral cavity, where their atypical presentation may pose a diagnostic challenge due to clinical overlap with other pigmented lesions. We report a case of an intramucosal palatal congenital melanocytic nevus (CMN) in a 34-year-old woman who presented with a painless nodular lesion arising from a lifelong pigmented area of the palate. Histopathological examination demonstrated a benign proliferation of nevus cells with theques formation. The deepest nevus cells showed proximity to the adjacent minor salivary gland lobules. The lesion was managed by complete surgical excision, with uneventful healing at 6-month follow-up. A comprehensive review of the literature identified only 11 reported cases of intraoral CMNs, confirming the palate as the most frequently involved site and a marked female predominance. This case highlights the critical role of correlating clinical history with histopathological findings to achieve an accurate diagnosis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.