Sellari-Franceschini S, Forli F, Pierini S, Favre C, Berrettini S, Macchia P A
Neuroscience Department, University of Pisa, Italy.
Int J Pediatr Otorhinolaryngol. 1999 Apr 25;48(1):83-7. doi: 10.1016/s0165-5876(99)00013-0.
Langerhans cell histiocytosis (LCH) is a rare disorder of unknown cause, characterized by the proliferation of histiocytic cells in various tissues and organs. The role of the otolaryngologist is important in the early and accurate evaluation, staging and diagnosis of LCH, because it may mimic more common diseases such as otitis externa and acute mastoiditis. We discuss a case report of bilateral mastoid involvement in a child with a history of otalgia unresponsive to medical therapy.
朗格汉斯细胞组织细胞增多症(LCH)是一种病因不明的罕见疾病,其特征是组织细胞在各种组织和器官中增殖。耳鼻喉科医生在LCH的早期准确评估、分期和诊断中起着重要作用,因为它可能类似于外耳道炎和急性乳突炎等更常见的疾病。我们讨论一例有耳痛病史且药物治疗无效的儿童双侧乳突受累的病例报告。