São Paulo Medical Journal ()

Langerhans cell histiocytosis

  • Maria de Lourdes L. F. Chauffaille,
  • Rosana M. Valério,
  • Cybelle Maria Costa Diniz,
  • Milvia Maria Simões,
  • Silva Enokihara,
  • Nylceo Michalany,
  • Karin Ventura Ferreira,
  • José Antonio Baddini Martinez,
  • Karine Marques Hassun,
  • Álvaro Nagib Atallah,
  • José Kerbauy

DOI
https://doi.org/10.1590/s1516-31801998000100006
Journal volume & issue
Vol. 116, no. 1
pp. 1625 – 1628

Abstract

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The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations. Skin biopsy immunohistochemistry presented positive S100 protein and vimentine, but the diagnosis was done with the demonstration of Birbeck granules with eletronic mucroscopy. The treatment was based on systemical chemotherapy although vulvar lesion has a bad response to chemotherapy.

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