Understanding alopecia areata characteristics in children under the age of 4 years

Sneha Rangu1, Rachel Rogers2, Leslie Castelo-Soccio1,3

  • 1Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Pediatric Dermatology
|August 31, 2019
PubMed

Insights

Most young children with alopecia areata (AA) present with mild disease. However, those with over 50% hair loss at initial presentation are more likely to experience worsening or persistent severe alopecia areata.

Area of Science:

  • Pediatric dermatology
  • Dermatology
  • Epidemiology

Background:

  • Epidemiologic data on pediatric alopecia areata (AA) is limited, especially for very young children.
  • No prior studies have specifically investigated the youngest children diagnosed with AA.

Purpose of the Study:

  • To evaluate the clinical presentations of alopecia areata (AA) in children younger than 4 years.
  • To identify prognostic factors associated with disease progression in pediatric AA.

Main Methods:

  • Retrospective chart review of 125 pediatric patients diagnosed with AA before age 4.
  • Disease severity assessed using the Severity of Alopecia Tool (SALT) score at baseline and at 3-6 months, 1 year, and 2 years post-presentation.

Main Results:

  • The majority of children presented with mild AA (less than 50% hair loss) and maintained mild disease over 2 years.
  • Children with over 50% hair loss at initial presentation had significantly higher likelihood of worsening SALT scores and persistent severe disease.
  • Associated conditions included atopic dermatitis (41%), family history of AA (28%), and family history of autoimmune diseases (27%).

Conclusions:

  • Most children under age 4 with alopecia areata (AA) present with mild disease, characterized by less than 50% scalp hair loss.
  • Children presenting with more severe AA are at higher risk for disease progression or sustained severity.
  • Findings support the use of prognostic factors for improved family counseling and education regarding pediatric AA.
Abstract

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