LCH Case Report in Adult- A Rare and Unusual Event

Neetu Pandey
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Abstract

Langerhans cell histiocytosis (LCH) is a histiocytic neoplasm characterized by clonal proliferation of Langerhans type cells, a normal antigen presenting cells. It most commonly affects children, with an annual incidence of 2–5 cases per million inhabitants, it is extremely rare in adults. Herein we are reporting a case of LCH in 37 year old male which was initially diagnosed by FNAC and confirmed by histopathology and IHC performed later on.
成人LCH病例报告-罕见和不寻常的事件
朗格汉斯细胞组织细胞增生症(LCH)是一种以朗格汉斯型细胞(一种正常的抗原呈递细胞)克隆性增殖为特征的组织细胞性肿瘤。它最常见于儿童,年发病率为每百万居民2-5例,在成人中极为罕见。在此,我们报告一例37岁男性LCH,最初通过FNAC诊断,后来通过组织病理学和免疫组化证实。
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