Langerhans cell histiocytosis presenting as a rapidly evolving frontotemporal syndrome

Neurol Sci. 2019 May;40(5):1055-1058. doi: 10.1007/s10072-019-3709-y. Epub 2019 Jan 10.

Abstract

Langerhans cell histiocytosis (LCH) is a rare disorder in adults which usually manifests with involvement of multiple organ systems, including the central nervous system. We describe an unusual case of biopsy-proven LCH presenting with frontotemporal-dominant cognitive impairment with hypothalamic involvement, along with multisystem disease. We propose that the dementia was probably an immune-mediated process triggered by LCH which responded dramatically to high-dose steroids.

Keywords: Cognition; Dementia; Hypothalamus; Langerhans cell histiocytosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Brain / diagnostic imaging
  • Brain / pathology
  • Cognitive Dysfunction / diagnosis*
  • Cognitive Dysfunction / drug therapy
  • Cognitive Dysfunction / pathology
  • Cognitive Dysfunction / physiopathology
  • Dementia / diagnosis*
  • Dementia / drug therapy
  • Dementia / pathology
  • Dementia / physiopathology
  • Diagnosis, Differential
  • Histiocytosis, Langerhans-Cell / diagnosis*
  • Histiocytosis, Langerhans-Cell / drug therapy
  • Histiocytosis, Langerhans-Cell / pathology
  • Histiocytosis, Langerhans-Cell / physiopathology
  • Humans
  • Male
  • Syndrome