Usubalieva Aisulu, Pierson Christopher R, Kavran Christina A, Huntoon Kristin, Kryvenko Oleksandr N, Mayer Theodore G, Zhao Weiqiang, Rock Jack, Ammirati Mario, Puduvalli Vinay K, Lehman Norman L
From the Departments of Pathology (AU, CRP, CAK, WZ, NLL), Anatomy (CRP), Neurosurgery (KH, MA), and Neuroscience (NLL), and Division of Neuro-oncology (VKP), The Ohio State University; and Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital (CRP), Columbus Ohio; and Departments of Pathology (ONK, TGM, NLL) and Neurosurgery (JR), Henry Ford Hospital, Detroit, Michigan.
J Neuropathol Exp Neurol. 2015 Oct;74(10):960-9. doi: 10.1097/NEN.0000000000000240.
Primary meningeal gliomas are rare tumors composed of a heterogeneous group of neoplasms. We present 2 clinically aggressive cases of primary meningeal pleomorphic xanthoastrocytoma that clinically mimicked meningioma. One case presented in the posterior fossa of a 56-year-old woman; the other centered on the left operculum of a 35-year-old woman. These cases showed many of the classic features of pleomorphic xanthoastrocytoma, except that xanthomatous cells were rare and eosinophilic granular bodies were inconspicuous. Both cases exhibited high proliferative indices and superficially invaded the brain. One case harboring a BRAF mutation disseminated to the thecal sac and showed a clinical response to the targeted BRAF inhibitor dabrafenib. These cases seem to represent an unusual primarily extra-axial presentation of pleomorphic xanthoastrocytoma and may account for at least some of the previously reported cases of primary meningeal glioma and/or glial fibrillary acidic protein-immunoreactive meningioma variants. We suggest that BRAF mutation analysis be considered in all meningeal lesions showing atypical histologic or immunohistochemical profiles, particularly those exhibiting glial differentiation, as a diagnostic aid and possible indication for targeted therapy.
原发性脑膜胶质瘤是由一组异质性肿瘤组成的罕见肿瘤。我们报告了2例具有临床侵袭性的原发性脑膜多形性黄色星形细胞瘤病例,其临床表现酷似脑膜瘤。1例发生在一名56岁女性的后颅窝;另一例位于一名35岁女性的左侧脑岛。这些病例表现出多形性黄色星形细胞瘤的许多典型特征,只是黄色瘤细胞罕见,嗜酸性颗粒体不明显。两例均表现出高增殖指数,并向脑表面浸润。1例携带BRAF突变,扩散至硬膜囊,并对靶向BRAF抑制剂达拉非尼产生临床反应。这些病例似乎代表了多形性黄色星形细胞瘤一种不寻常的主要轴外表现,可能至少解释了一些先前报道的原发性脑膜胶质瘤和/或胶质纤维酸性蛋白免疫反应性脑膜瘤变异型病例。我们建议,对于所有显示非典型组织学或免疫组化特征的脑膜病变,尤其是那些表现出胶质分化的病变,应考虑进行BRAF突变分析,作为诊断辅助手段以及靶向治疗的可能指征。