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Cutaneous Langerhans cell histiocytosis presenting with hypopigmented lesions: Report of two cases and review of literature

  • Shoko Mori
  • , Tony Adar
  • , Viktoryia Kazlouskaya
  • , Jaime B. Alexander
  • , Edward Heilman
  • , Sharon A. Glick
  • SUNY Downstate Health Sciences University

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Langerhans cell histiocytosis is a rare group of disorders that results from the abnormal proliferation and accumulation of dendritic-derived cells in various organs of the body, such as the skin and bones. Hypopigmented macules are a rare cutaneous presentation of Langerhans cell histiocytosis that may pose a diagnostic dilemma when no other findings of Langerhans cell histiocytosis are present at the time of examination. We present 2 cases of the hypopigmented variant of Langerhans cell histiocytosis, including a case with histopathologic features of regression, and a review of the literature. These cases highlight the importance of including Langerhans cell histiocytosis in the differential diagnosis of an infant with hypopigmented macules and papules.

Original languageEnglish
Pages (from-to)502-506
Number of pages5
JournalPediatric Dermatology
Volume35
Issue number4
DOIs
StatePublished - Jul 1 2018

Keywords

  • histiocytic disorders
  • skin signs of systemic disease

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