Marcas congénitas: Uma alteração comum em recém-nascidos

Epidermal nevi are generally benign, isolated conditions, occurring in approximately 1 to 3 per 1,000 newborns, with sebaceous nevi accounting for approximately half of cases. The authors present two clinical cases of newborns with different subtypes of congenital epidermal nevi: a papillomatous epidermal nevus and a sebaceous nevus. Epidermal nevi typically present as a single benign lesion. However, in some cases − especially when the lesions are large or extensive − they may be associated with syndromic forms involving other organs, most commonly the brain, eye, and skeletal systems. Early recognition of these skin lesions at birth is crucial, as it allows fot appropriate clinical management and early detection of any extracutaneous abnormalities.

Publication Details

Journal
Scientific Repository of Open Access of Portugal (RCAAP)
Published
2025-01-15
DOI
https://doi.org/10.25753/birthgrowthmj.v33.i4.32984
Primary Topic
Genetic and rare skin diseases.
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Marcas congénitas: Uma alteração comum em recém-nascidos

Scientific Repository of Open Access of Portugal (RCAAP)
Genetic and rare skin diseases.
article

Marcas congénitas: Uma alteração comum em recém-nascidos

article en

Abstract

Epidermal nevi are generally benign, isolated conditions, occurring in approximately 1 to 3 per 1,000 newborns, with sebaceous nevi accounting for approximately half of cases. The authors present two clinical cases of newborns with different subtypes of congenital epidermal nevi: a papillomatous epidermal nevus and a sebaceous nevus. Epidermal nevi typically present as a single benign lesion. However, in some cases − especially when the lesions are large or extensive − they may be associated with syndromic forms involving other organs, most commonly the brain, eye, and skeletal systems. Early recognition of these skin lesions at birth is crucial, as it allows fot appropriate clinical management and early detection of any extracutaneous abnormalities.

Scientific Repository of Open Access of Portugal (RCAAP)
Good health and well-being
Openalex Percentile: Top 56%
Genetic and rare skin diseases.
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.