Ben Meriem C, Nouri S, Chouchane C, Chouchane S, Said M, Ghédira L, Moussa A, Boubtane M, Guediche M N
Service de pédiatrie, CHU de Fattouma-Bourguiba, 5000, Monastir, Tunisie.
Arch Pediatr. 2006 Jan;13(1):44-7. doi: 10.1016/j.arcped.2005.09.030. Epub 2005 Dec 15.
Langerhans cell histiocytose is a rare condition in childhood. It presents in different ways ranging from a single bony disease to a multisystemic disease involving vital organs.
We report a case of single bone involvement revealed by torticollis in an eight-year-old boy. The diagnosis was evocated on radiological findings and confirmed by histologic aspects. After a period of 2,5 years, this child is in total spontaneous remission.
Torticollis must be explored and watched. Eosinophilic granuloma can be a rare aetiology in children. The outcome is often favorable.
朗格汉斯细胞组织细胞增多症在儿童期是一种罕见疾病。它有多种表现形式，从单一骨病到累及重要器官的多系统疾病。
我们报告一例8岁男孩因斜颈发现的单骨受累病例。根据影像学表现提出诊断，并经组织学特征证实。经过2.5年，该患儿完全自发缓解。
对于斜颈必须进行检查和观察。嗜酸性肉芽肿在儿童中可能是一种罕见病因。其预后通常良好。
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