Strehl Johanna D, Stachel Klaus-Daniel, Hartmann Arndt, Agaimy Abbas
Institute of Pathology, Erlangen, Germany.
Int J Clin Exp Pathol. 2012;5(7):720-5. Epub 2012 Sep 5.
The synchronous or metachronous development of Langerhans cell histiocytosis and non-Langerhans cell histiocytosis in the same patient is rare. To date, only seven cases of xanthogranulomas developing in young patients with a history of Langerhans cell histiocytosis and systemic therapy have been reported in the literature. As of yet, the pathogenesis and the clinical significance of this phenomenon are unclear. We report the case of a 3 year old boy who developed juvenile Xanthogranulomas on the forehead and right upper eye lid 1.5 years after systemic therapy for monosystemic Langerhans cell histiocytosis of the bone and complete disease remission.
朗格汉斯细胞组织细胞增多症和非朗格汉斯细胞组织细胞增多症在同一患者中同步或异时发生的情况很少见。迄今为止,文献中仅报道了7例在有朗格汉斯细胞组织细胞增多症病史并接受过全身治疗的年轻患者中发生黄瘤的病例。截至目前,这种现象的发病机制和临床意义尚不清楚。我们报告了一名3岁男孩的病例,该男孩在接受骨单系统朗格汉斯细胞组织细胞增多症全身治疗并完全缓解疾病1.5年后,在前额和右上眼睑出现了幼年性黄色肉芽肿。