Literature DB >> 15874853

Langerhans cell histiocytosis of the vulva: two case reports.

Jennifer E Dietrich1, Creighton Edwards, Rodolfo Laucirica, Raymond H Kaufman.   

Abstract

This report describes the histopathologic results of Langerhans cell histiocytosis of the vulva and options for treatment. We present two new cases demonstrating vulvar manifestations of disease and their course of treatment with a review of the literature. Langerhans cell histiocytosis of the female genital tract is rare. The disease cannot be diagnosed without biopsy of cutaneous lesions. Langerhans cell histiocytosis of the vulva is a rare disorder with few options for treatment.

Entities:  

Year:  2004        PMID: 15874853     DOI: 10.1097/00128360-200404000-00011

Source DB:  PubMed          Journal:  J Low Genit Tract Dis        ISSN: 1089-2591            Impact factor:   1.925


  1 in total

1.  Diagnosis of primary langerhans cell histiocytosis of the vulva in a postmenopausal woman.

Authors:  Sefa Kurt; Mehmet Tunc Canda; Aycan Kopuz; Dudu Solakoglu Kahraman; Abdullah Tasyurt
Journal:  Case Rep Obstet Gynecol       Date:  2013-09-15
  1 in total

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