Gurung Ishwor, Gao Yan, Han Kai, Peng Xue-Biao
Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Indian J Dermatol. 2019 Sep-Oct;64(5):414-416. doi: 10.4103/ijd.IJD_504_18.
Langerhans cell histiocytosis (LCH) is a proliferative disease commonly seen in the pediatric population but rarely encountered in the adult population. The exact etiology remains unclear. It has various clinical features and is very likely to be misdiagnosed. Histopathology and immunohistochemistry are very important for the diagnosis of LCH. Treatment protocols remain controversial. Herein, we report a rare adult onset LCH, which is confined to the skin. A 50-year-old Chinese man presented with a nodule with itchy rashes on the left lower leg, which gradually grew in size for the last 6 months. He also had multiple scattered rashes on the right lower leg. The skin biopsy demonstrated Langerhans cells infiltrating the superficial dermis, and the tumor cells were positive for CD1a and S-100 expression. The diagnosis was LCH based on the histopathological and immunohistochemistry results.
朗格汉斯细胞组织细胞增多症(LCH)是一种增殖性疾病,常见于儿童群体,但在成人中很少见。确切病因尚不清楚。它有多种临床特征,很容易被误诊。组织病理学和免疫组织化学对LCH的诊断非常重要。治疗方案仍存在争议。在此,我们报告一例罕见的成人起病的局限于皮肤的LCH。一名50岁的中国男性,左小腿出现一个伴有瘙痒皮疹的结节,在过去6个月中逐渐增大。他的右小腿也有多个散在的皮疹。皮肤活检显示朗格汉斯细胞浸润浅表真皮,肿瘤细胞CD1a和S-100表达呈阳性。根据组织病理学和免疫组织化学结果,诊断为LCH。