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Posterior fossa choroid plexus papilloma with focal ependymal differentiation in an adult patient: A case report and literature review

机译:成年患者后颅窝脉络丛乳头状瘤伴局灶性室间隔膜分化:一例报道并文献复习

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摘要

Choroid plexus papillomas (CPPs) are rare neoplasms classified as World Health Organization grade I tumors. CPPs containing other tissues have occasionally been documented in the literature. However, few of these previous reports have provided clinical and radiological information. We herein report a case of a posterior fossa CPP with focal ependymal differentiation in a 42-year-old woman who presented with a 6-month history of progressive headache. Preoperative radiological images showed a hypervascular tumor protruding into the left foramen of Luschka with perilesional edema. Gross total resection of the tumor was performed. Histopathological examination revealed that the tumor was composed of papillary structures. Immunohistochemical staining of glial fibrillary acidic protein was focally positive around the capillaries, which was suggestive of “perivascular pseudorosette” formation. Our case showed similar imaging appearances as those of CPP; thus, it seems difficult to distinguish CPP with versus without ependymal differentiation by clinical and radiological features alone. The clinical significance and pathogenesis of ependymal differentiation in CPP remain unclear, and further case reports are required.
机译:脉络丛乳头状瘤(CPPs)是被分类为世界卫生组织I级肿瘤的罕见肿瘤。含有其他组织的CPP偶尔在文献中有记载。但是,这些以前的报告很少提供临床和放射学信息。我们在此报告了42岁女性中有6个月进行性头痛病史的,具有局灶性室间隔分化的后窝CPP病例。术前影像学检查显示,一个高血管瘤突出到卢斯卡左孔,伴有病灶周围水肿。进行肿瘤的大体全切除。组织病理学检查显示该肿瘤由乳头状结构组成。胶质纤维酸性蛋白的免疫组织化学染色在毛细血管周围呈局灶性阳性,提示“血管周围假红斑”形成。我们的病例显示出与CPP相似的影像学表现。因此,仅凭临床和放射学特征就很难区分具有室间隔分化和不具有室间隔分裂的CPP。 CPP中室管膜分化的临床意义和发病机制尚不清楚,需要进一步的病例报告。

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