Langerhans cell histiocytosis of vulva and cervix in a 19-year-old woman

Gynecol Obstet Invest. 1997;44(1):67-9. doi: 10.1159/000291414.

Abstract

Langerhans cell histiocytosis of the female genital tract is a rare disease. A clinical diagnosis is impossible to establish because no typical lesions are found. Immunohistochemistry of bioptic samples is the easier technique to obtain the correct diagnosis. We present a case of a 19-year-old woman with Langerhans cell histiocytosis of mandible and maxilla with subsequent cervical and vulvar histiocytosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Histiocytosis, Langerhans-Cell / diagnosis*
  • Histiocytosis, Langerhans-Cell / pathology
  • Humans
  • Immunoenzyme Techniques
  • Mandibular Diseases / complications
  • Mandibular Diseases / pathology
  • Maxillary Diseases / complications
  • Maxillary Diseases / pathology
  • S100 Proteins / analysis
  • Uterine Cervical Diseases / complications
  • Uterine Cervical Diseases / diagnosis*
  • Uterine Cervical Diseases / pathology
  • Vulvar Diseases / complications
  • Vulvar Diseases / diagnosis*
  • Vulvar Diseases / pathology

Substances

  • S100 Proteins