Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1111/cup.13670 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Risk factors associated with tumor upstaging in melanomas treated with Mohs micrographic surgery with melanocytic immunohistochemistry.
JAAD Int
September 2024
Department of Dermatology, Mayo Clinic, Rochester, Minnesota.
Background: Mohs micrographic surgery with melanocytic immunohistochemistry (MMS-I) is increasingly utilized for special site melanoma treatment. Yet, frequency and risk factors associated with upstaging of all-stage cutaneous melanomas treated with MMS-I remain undefined.
Objective: Determine upstaging frequency and factors associated with tumor upstaging for all-stage melanomas treated with MMS-I.
Pediatric spitzoid lesions of the ear: a single-center experience and review of the literature.
Dermatol Reports
September 2023
Dermatology Unit, Pediatric Hospital IRCSS Giannina Gaslini, Genoa, Italy.
Spitzoid lesions are challenging melanocytic lesions comprising benign, intermediate, and malignant lesions. In this study, we aimed to analyze the diagnostic accuracy of clinical and dermatoscopical evaluations of pediatric spitzoid ear lesions. We collected and analyzed, clinically, dermatoscopically, and histologically, pediatric spitzoid ear lesions.
View Article and Find Full Text PDFSeries of 50 special-site nevi cases: Is it a unique entity or only one variant of dysplastic nevi?
J Cutan Pathol
July 2020
Surgical Pathology Department, Pathology Institute of Araçatuba, Araçatuba, Brazil.
Atypical umbilical naevi: histopathological analysis of 20 cases.
Histopathology
February 2015
Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
Aims: Melanocytic naevi on the umbilicus have been described as a form of flexural naevi, with the most common feature being a 'nested and dyshesive pattern'. We have encountered a distinct group of umbilical naevi with more significant atypia and prominent fibrosis, not reported previously. This study aimed to characterize these naevi more clearly.
View Article and Find Full Text PDFAnalysis of loss of heterozygosity in single-system and multisystem Langerhans' cell histiocytosis.
Pediatr Dev Pathol
May 2007
University of Pittsburgh School of Medicine and Department of Pathology, Presbyterian University Hospital, PA 15213, USA.
Article Synopsis
- This study investigates the role of genetic mutations, specifically fractional allelic loss (FAL), in the progression of Langerhans' cell histiocytosis (LCH) by comparing different clinical stages and the involvement of various organs.
- Using PCR and genetic analysis, the research found that children with multisystem LCH (MS-LCH) exhibited a significantly higher FAL compared to those with single-system LCH (SS-LCH), indicating a correlation between genetic mutations and disease severity.
- The study suggests that LCH cases with high-risk organ involvement show more genetic alterations, and further research is needed to explore the potential of specific genetic markers for predicting disease progression.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!