Autopsy and Case Reports (Jun 2016)

Indeterminate cell histiocytosis successfully treated with phototherapy

  • Maria Claudia Nogueira Zerbini,
  • Mirian Nacagami Sotto,
  • Fernando Peixoto Ferraz de Campos,
  • Andre Neder Ramires Abdo,
  • Juliana Pereira,
  • José Antônio Sanches Junior,
  • Jade Cury Martins

DOI
https://doi.org/10.4322/acr.2016.038
Journal volume & issue
Vol. 6, no. 2

Abstract

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First described in 1985, intermediate cell histiocytosis is a rare disorder of the cutaneous dendritic cell group with a varied clinical presentation and evolution. The pathologic substrate is constituted by the proliferation of indeterminate cells (ICs) that are immunophenotypically characterized by the positivity of CD1a, CD68, and faint/focal S100, plus the negativity for CD207 (langerin). The authors present the case of a healthy elderly woman who presented generalized dome-shaped reddish cutaneous nodules over her trunk, neck, face, and extremities over a period of 18 months. A laboratory and imaging work-up ruled out internal involvement. The skin biopsy was consistent with IC histiocytosis. The patient was treated with narrowband ultraviolet B phototherapy, which resulted in an excellent short-term outcome

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