Isolated Langerhans Cell Histiocytosis of the Vulva in a 28-Year-Old Lady: A Report of a Case and Brief Review of the Literature
Langerhans cell histiocytosis (LCH) is a rare, proliferative disorder of Langerhans’ cells. The presentation can vary from single organ involvement to multisystem and disseminated in severe cases, affecting children more than adults. Isolated vulvar involvement of LCH in a 28-year-old woman has rare...
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Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2022-01-01
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Series: | Case Reports in Dermatological Medicine |
Online Access: | http://dx.doi.org/10.1155/2022/8483008 |
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Summary: | Langerhans cell histiocytosis (LCH) is a rare, proliferative disorder of Langerhans’ cells. The presentation can vary from single organ involvement to multisystem and disseminated in severe cases, affecting children more than adults. Isolated vulvar involvement of LCH in a 28-year-old woman has rarely been described and also there are limited data for diagnosis and treatment. Herein, we report the case of a 28-year-old woman with isolated vulvar LCH, misdiagnosed with herpes simplex infection, successfully treated with thalidomide. |
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ISSN: | 2090-6471 |