Brain Pathol. 2012 May;22(3):433-7. doi: 10.1111/j.1750-3639.2012.00591.x.
Isolated intracranial xanthogranulomas arising from the dura mater are extremely rare.We present a case of a symptomatic large right frontoparietal dura based intracranial xanthogranuloma in a 38-year-old female. Xanthogranulomas are benign non-Langerhans cell histiocytic lesions. They are frequently described in the skin of infants and children. Extracutaneous manifestations especially in the central nervous system are highly uncommon. Dural xanthogranulomas usually arise in association with familial hypercholesterolemia, with Erdheim Chester disease (ECD), and with Weber-Christian disease. Our case however, had no such associations. In this report, the authors describe the clinical, radiological and microscopic presentation of this case and the differential diagnoses of intracranial xanthogranuloma.
颅内孤立性脑膜黄瘤极为罕见。我们报告了一例 38 岁女性右侧额顶骨大的脑膜基颅内黄瘤。黄瘤是良性的非朗格汉斯细胞组织细胞病变。它们常发生在婴儿和儿童的皮肤中。中枢神经系统的皮肤外表现非常罕见。硬脑膜黄瘤通常与家族性高胆固醇血症、Erdheim-Chester 病(ECD)和 Weber-Christian 病相关。然而,我们的病例没有这些关联。在本报告中,作者描述了该病例的临床、放射学和显微镜表现以及颅内黄瘤的鉴别诊断。