Davis Steven E, Rice Dale H
Department of Otolaryngology-Head and Neck Surgery, Keck School of Medicine, University of Southern California, 1200 N. State St., Los Angeles, CA 90033, USA.
Ear Nose Throat J. 2004 May;83(5):340, 342, 344 passim.
Langerhans' cell histiocytosis (LCH)--once called histiocytosis X--is a complex reticuloendothelial disease that often involves the head and neck. We discuss the current nomenclature of this disease and review its pathologic and clinical characteristics, with particular emphasis on the role of the head and neck surgeon. LCH can be challenging to diagnose, and the otolaryngologist must be familiar with its varied presentations. Because LCH usually responds well to medical therapy and extensive resection can easily cause more morbidity than the disease itself, a minimalist approach to treatment usually provides the best outcome. We also discuss the case of a 9-month-old girl with LCH who presented with aggressive head and neck disease.
朗格汉斯细胞组织细胞增多症(LCH)——曾被称为组织细胞增多症X——是一种复杂的网状内皮系统疾病,常累及头颈部。我们讨论了该疾病的当前命名,并回顾了其病理和临床特征,特别强调了头颈外科医生的作用。LCH的诊断可能具有挑战性,耳鼻喉科医生必须熟悉其多样的表现形式。由于LCH通常对药物治疗反应良好,广泛切除很容易导致比疾病本身更多的发病率,因此采用极简主义的治疗方法通常能取得最佳效果。我们还讨论了一名9个月大患LCH的女孩的病例,她患有侵袭性头颈部疾病。