Chen W Z, Lv Y X, Xu D B, Chen W Z, Yu J C
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Mar 5;31(5):397-399. doi: 10.13201/j.issn.1001-1781.2017.05.018.
Langerhans cell histiocytosis (LCH) is a rare monoclonal disease,its clinical presentation is highly variable because it can affect multiple organs, such as lung, bone, skin, lymph nodes, hypothalamopituitary axis, and other multiple sites. LCH involving the thyroid gland is extremely rare, here we reported a rare case of LCH involving thyroid, presenting as painless thyroid goiters.
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的单克隆疾病,其临床表现高度多变,因为它可累及多个器官,如肺、骨、皮肤、淋巴结、下丘脑 - 垂体轴及其他多个部位。累及甲状腺的LCH极为罕见,在此我们报告1例罕见的累及甲状腺的LCH,表现为无痛性甲状腺肿大。