Ng W K, Lam K Y, Ng I O
Department of Pathology, University of Hong Kong, Queen Mary Compound, Hong Kong.
J Clin Pathol. 1995 Oct;48(10):963-5. doi: 10.1136/jcp.48.10.963.
A rare case of adult onset Langerhans' cell histiocytosis associated with dysgerminoma in a 35 year old Chinese woman is reported. The patient had a history of dysgerminoma of left ovary 15 years previously and had undergone surgery followed by radiotherapy and an uneventful recovery. She presented again in March 1994, this time with a left clavicular mass, which was shown histologically to be Langerhans' cell histiocytosis. The report illustrates the probable association between the two lesions, with some discussion on the underlying pathogenesis.
报告了一例35岁中国女性成人期朗格汉斯细胞组织细胞增多症合并无性细胞瘤的罕见病例。该患者15年前有左侧卵巢无性细胞瘤病史，接受了手术，随后进行了放疗，恢复顺利。1994年3月她再次就诊，此次出现左锁骨肿块，组织学检查显示为朗格汉斯细胞组织细胞增多症。该报告阐述了这两种病变之间可能的关联，并对潜在发病机制进行了一些讨论。
