Reticular Pigmentary Anomalies in Pediatrics

Authors

  • Maria Isabel Pastura Dr. Ricardo Gutiérrez General Children’s Hospital Buenos Aires Argentina

Keywords:

Dowling Degos Disease, Gougerot Carteaud, Acanthosis nigricans, Kitamura disease, Dohi disease, Naegeli-Franceschetti-Jadassohn Syndrome, Galli-Galli disease, Haber syndrome

Abstract

Reticular pigmentary anomalies in childhood consists of different entities that clinically present with a common factor of a hyperpigmented reticular skin pattern. This is why they are particularly perplexing for the dermatologist in their daily practice. However, they differ from each other in terms of their age of onset, predominant location, preferred ethnicity, evolution, associated systemic involvement, distinctive histopathological and molecular characteristics, and their therapeutic response.

  A clinical case about a teenage male diagnosed with Dowling-Degos Disease, evaluated at the Pediatric Dermatology Service of Dr. Ricardo Gutiérrez Children's Hospital is reported as an example.

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Author Biography

Maria Isabel Pastura, Dr. Ricardo Gutiérrez General Children’s Hospital Buenos Aires Argentina

Corresponding author:

Maria Isabel Pastura,

Specialist in pediatrics and pediatric dermatology,

Former Chief Resident of Pediatric Dermatology

at the Dr. Ricardo Gutiérrez General Children’s Hospital,

Buenos Aires, Argentina

E-mail: marpastura@gmail.com

Published

2025-03-07

How to Cite

Pastura, M. I. (2025). Reticular Pigmentary Anomalies in Pediatrics. International Journal of Pediatric Dermatology, 2(1), Ahead of print. Retrieved from https://scientificeditorial.com/index.php/IJPD/article/view/Reticular-Pigmentary-Anomalies-in-Pediatrics
Received 2024-09-20
Accepted 2025-03-07
Published 2025-03-07