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Diagnosis of Primary Langerhans Cell Histiocytosis of the Vulva in a Postmenopausal Woman
Author(s) -
Sefa Kurt,
Mehmet Tunç Canda,
Aycan Kopuz,
Dudu Solakoğlu Kahraman,
Abdullah Taşyurt
Publication year - 2013
Publication title -
case reports in obstetrics and gynecology
Language(s) - English
Resource type - Journals
eISSN - 2090-6684
pISSN - 2090-6692
DOI - 10.1155/2013/962670
Subject(s) - vulva , langerhans cell histiocytosis , medicine , postmenopausal women , differential diagnosis , female circumcision , histiocytosis , dermatology , rare disease , disease , pathology , gynecology
Langerhans cell histiocytosis (LCH) is a very rare disease of female genital tract, most commonly seen in vulva and unusual in postmenopausal period. Herein, we report the 8th case of pure vulvar LCH in a postmenopausal woman. We pay attention to the differential diagnosis in postmenopausal state, features of pathologic diagnosis, and treatment options.

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