Lin Chien-Heng, Lin Wei-Ching, Chiang I-Ping, Ho Yung-Jen, Peng Ching-Tien, Wu Kang-Hsi
Department of Pediatrics, Jen-Ai Hospital, Taichung, Taiwan.
J Pediatr Hematol Oncol. 2010 May;32(4):309-11. doi: 10.1097/MPH.0b013e3181c4de1a.
Langerhans cell histiocytosis (LCH), a monoclonal disease of histiocytes, may involve several organ systems but rarely primarily involves the thyroid gland. This report presents an extremely rare case of LCH of the thyroid and lungs in a 3-year-old boy who presented with a neck mass for several weeks. The patient subsequently underwent chemotherapy with resolution of the goiter and lung findings, and the patient remained in complete remission 1 year after chemotherapy. LCH of the thyroid should be considered in the differential diagnosis of a child with a thyroid mass. Pulmonary examination should be done in these patients.
朗格汉斯细胞组织细胞增多症(LCH)是一种组织细胞的单克隆疾病,可累及多个器官系统,但很少以甲状腺为主要受累部位。本报告介绍了一名3岁男孩甲状腺和肺部LCH的极其罕见病例,该男孩颈部肿块数周。患者随后接受化疗,甲状腺肿和肺部病变消退,化疗后1年患者仍处于完全缓解状态。对于有甲状腺肿块的儿童,鉴别诊断时应考虑甲状腺LCH。这些患者应进行肺部检查。