Galloway Luke, Zilani Gulam, Lammie Alistair, Leach Paul
Department of Neurosurgery, University Hospital of Wales, Cardiff, UK.
Department of Histopathology, University Hospital of Wales, Cardiff, UK.
Childs Nerv Syst. 2020 Jun;36(6):1311-1314. doi: 10.1007/s00381-019-04486-5. Epub 2020 Jan 2.
Meningioangiomatosis is a rare histologically distinct abnormality that is occasionally associated with intracranial meningioma. The rhabdoid variant of meningioma is also uncommon and is classified as a World Health Organization Grade III tumour. We report a case of meningioangiomatosis in conjunction with a meningioma with prominent rhabdoid features, in an infant male who underwent complete surgical resection of the lesion. The patient has been followed up for 6 years with no disease recurrence. To our knowledge, this is the first report in the literature describing meningioangiomatosis combined with a meningioma with rhabdoid features.
脑膜血管外皮细胞瘤是一种罕见的组织学上独特的异常病变，偶尔与颅内脑膜瘤相关。脑膜瘤的横纹肌样变体也不常见，被归类为世界卫生组织III级肿瘤。我们报告了一例婴儿男性患者，其患有脑膜血管外皮细胞瘤并伴有具有显著横纹肌样特征的脑膜瘤，该患者接受了病变的完全手术切除。患者已随访6年，无疾病复发。据我们所知，这是文献中首例描述脑膜血管外皮细胞瘤合并具有横纹肌样特征的脑膜瘤的报告。
