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Eosinophilic granuloma revealed by torticollis: a case report
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...
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Published in: | Archives de pédiatrie : organe officiel de la Société française de pédiatrie 2006-01, Vol.13 (1), p.44-47 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | fre |
Subjects: | |
Online Access: | Get full text |
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Summary: | 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. |
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ISSN: | 0929-693X |
DOI: | 10.1016/j.arcped.2005.09.030 |