Isolated Langerhans Cell Histiocytosis of the Vulva in a 28-Year-Old Lady: A Report of a Case and Brief Review of the Literature.

Q3 Medicine
Case Reports in Dermatological Medicine Pub Date : 2022-06-28 eCollection Date: 2022-01-01 DOI:10.1155/2022/8483008
Maryam Sadat Sadati, Nafiseh Todarbary, Fatemeh Sari Aslani, Maryam Hadibarhaghtalab
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引用次数: 0

Abstract

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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28岁女性外阴分离朗格汉斯细胞组织细胞增多症1例报告及文献复习。
朗格汉斯细胞组织细胞增生症(LCH)是一种罕见的朗格汉斯细胞增生性疾病。表现可从单一器官受累到多系统,严重时可播散,儿童多于成人。孤立外阴累及LCH的28岁妇女很少被描述,也有有限的数据诊断和治疗。在此,我们报告一例28岁女性孤立外阴LCH,误诊为单纯疱疹感染,成功治疗沙利度胺。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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