Lahiani D, Hammami B K, Maâloul I, Frikha M, Baklouti S, Jlidi R, Ben Jemaâ M
Service des maladies infectieuses, CHU Hédi-Chaker, 3029 Sfax, Tunisie.
Rev Med Interne. 2008 Mar;29(3):249-51. doi: 10.1016/j.revmed.2007.09.023. Epub 2007 Oct 22.
Langerhans cell histiocytosis or histiocytosis X has a variable course from a self-limited eosinophilic granuloma to an aggressive disseminated disease. It mainly affects children. We report a 76-year-old woman with multifocal bone histiocytosis X, involving the rachis, an iliac bone and the skull. The diagnosis has been established by histological exam. Outcome was favourable after chemotherapy.
朗格汉斯细胞组织细胞增多症或组织细胞增多症X的病程不一，从自限性嗜酸性肉芽肿到侵袭性播散性疾病。它主要影响儿童。我们报告了一名76岁的女性，患有多灶性骨组织细胞增多症X，累及脊柱、髂骨和颅骨。诊断通过组织学检查确定。化疗后结果良好。
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