ArticleClinical case reports2025
Neurocutaneous Melanosis in Children and Adults With Clinical, Radiological, and Pathogenic Evaluation: Case Report and Review of the Literature.
Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed.
- Prenatal Fetal Neurocutaneous Melanosis: A Case Report and Literature Review.Molecular genetics & genomic medicine · 2026Review
- Neurocutaneous Melanosis in Children and Adults With Clinical, Radiological, and Pathogenic Evaluation: Case Report and Review of the Literature.Clinical case reports · 2025Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Neurocutaneous melanosis (NCM) is a rare, non-inherited disease characterized by the presence of giant congenital melanocytic nevi (CMN) or multiple CMN, and it is often associated with meningeal melanosis or meningeal melanoma. This report presents two representative cases of NCM: one involving a 6-year-old female patient and the other involving a 30-year-old male patient. Both patients were born with severe CMN, including lesions on their hairy trunk, and later acquired malignant leptomeningeal involvement. We evaluated the clinical, radiological, and pathological features of cutaneous and central nervous system (CNS) lesions in these two patients, emphasizing their similarities and distinct manifestations. The research analysis highlights that individualized monitoring and related intervention strategies may improve the clinical prognosis of patients with this uncommon and potentially fatal disease through the process of early identification of high-risk features associated with malignant transformation.
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Registered trials
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