Eczema and Urticaria as Manifestations of Undiagnosed and Rare Diseases

Pediatr Clin North Am. 2017 Feb;64(1):39-56. doi: 10.1016/j.pcl.2016.08.004.

Abstract

Eczema and urticaria are common disorders encountered in pediatric patients, but they may occasionally be the presenting complaint in a child with an underlying rare disease. Immunodeficiency syndromes should be suspected when eczema is associated with neonatal onset, recurrent infections, chronic lymphadenopathy, or failure to thrive. Nutritional deficiencies and mycosis fungoides are in the differential diagnosis for a child with a recalcitrant eczematous eruption. Autoinflammatory syndromes should be suspected in a child with chronic urticaria, fever, and other systemic signs of inflammation. Although these disorders are rare, early recognition allows for appropriate treatment and decreased morbidity for the child.

Keywords: Autoinflammatory syndromes; Eczema; Immunodeficiency syndromes; Mycosis fungoides; Nutritional deficiencies; Urticaria.

Publication types

  • Review

MeSH terms

  • Child
  • Child Nutrition Disorders / diagnosis
  • Diagnosis, Differential
  • Eczema / diagnosis*
  • Hereditary Autoinflammatory Diseases / diagnosis
  • Humans
  • Immunologic Deficiency Syndromes / diagnosis
  • Mycosis Fungoides / diagnosis
  • Rare Diseases / diagnosis*
  • Urticaria / diagnosis*