Matsushita Shu, Shimono Taro, Goto Takeo, Doishita Satoshi, Kuwae Yuko, Miki Yukio
Department of Diagnostic and Interventional Radiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan.
Department of Neurosurgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Radiol Case Rep. 2018 Dec 4;14(3):304-308. doi: 10.1016/j.radcr.2018.11.017. eCollection 2019 Mar.
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.
脉络丛乳头状瘤(CPPs)是罕见的肿瘤,被归类为世界卫生组织一级肿瘤。文献中偶尔有关于含有其他组织的CPPs的记载。然而,这些既往报告中很少提供临床和放射学信息。我们在此报告一例42岁女性后颅窝CPPs伴局灶性室管膜分化的病例,该患者有6个月进行性头痛病史。术前放射学图像显示一个高血运肿瘤突入左侧Luschka孔并伴有瘤周水肿。对肿瘤进行了全切除。组织病理学检查显示肿瘤由乳头状结构组成。胶质纤维酸性蛋白免疫组化染色在毛细血管周围局灶阳性,提示“血管周围假菊形团”形成。我们的病例显示出与CPP相似的影像学表现;因此,仅通过临床和放射学特征似乎难以区分有和没有室管膜分化的CPP。CPP中室管膜分化的临床意义和发病机制仍不清楚,需要更多病例报告。