Shi Yu-Zhen, Chen Mao-Zhen, Huang Wei, Guo Li-Li, Chen Xiao, Kong Dan, Zhuang Ying-Ying, Xu Yi-Ming, Zhang Rui-Rui, Bo Gen-Ji, Wang Zhong-Qiu
1 Department of Medical Imaging, Huai'an First People's Hospital, Nanjing Medical University, Jiangsu, PR China.
2 Department of Radiology, Affiliated Hospital of Nanjing University of Traditional Chinese Medicine (TCM), Jiangsu, PR China.
Acta Radiol. 2017 Aug;58(8):983-990. doi: 10.1177/0284185116676651. Epub 2017 Mar 30.
Background Atypical choroid plexus papilloma (APP) is a rare, newly introduced entity with intermediate characteristics. To date, few reports have revealed the magnetic resonance (MR) findings. Purpose To analyze the clinicopathological and MR features of APP. Material and Methods The clinicopathological data and preoperative MR images of six patients with pathologically proven APP were retrospectively reviewed. The MR features including tumor location, contour, signal intensity, degree of enhancement, intratumoral cysts, and necrosis; and flow voids, borders, peritumoral edema, and associated hydrocephalus were analyzed. Results The APP were located in the ventricle (n = 4) and cerebellopontine angle (CPA, n = 2). Tumor dissemination along the spinal subarachnoid space was found in one patient. The tumors appeared as milt-lobulated (n = 5) or round mass (n = 1), with slightly heterogeneous signals (n = 5) or mixed signals (n = 1) on T1-weighted and T2-weighted images. Heterogeneous and strong enhancement were found in five cases on contrast-enhanced images. Three of four intraventricular tumors had a partly blurred border with ventricle wall. Four tumors had mild to moderate extent of surrounding edema signals. A slight hydrocephalus was seen in four patients. Incomplete capsule was seen in four tumors at surgery. Histopathologically, mild nuclear atypia was seen in all tumors with a mitotic rate of 2-5 per 10 high-power fields. Conclusion APP should be included in the differential diagnosis when an intraventricular or CPA tumor appearing as a multi-lobulated solid mass with slight heterogeneity, heterogeneous strong enhancement, partly blurred borders, mild to moderate peritumoral edema, or slight hydrocephalus are present.
背景 非典型脉络丛乳头状瘤(APP)是一种罕见的、新定义的具有中间特征的实体瘤。迄今为止,鲜有报道揭示其磁共振(MR)表现。目的 分析APP的临床病理及MR特征。材料与方法 回顾性分析6例经病理证实为APP患者的临床病理资料及术前MR图像。分析MR特征,包括肿瘤位置、轮廓、信号强度、强化程度、瘤内囊肿及坏死情况;以及流空信号、边界、瘤周水肿及相关脑积水情况。结果 APP位于脑室(n = 4)和桥小脑角(CPA,n = 2)。1例患者发现肿瘤沿脊髓蛛网膜下腔播散。肿瘤表现为分叶状(n = 5)或圆形肿块(n = 1),在T1加权和T2加权图像上信号略不均匀(n = 5)或混合信号(n = 1)。增强图像上5例呈不均匀强化且强化明显。4例脑室内肿瘤中有3例与脑室壁边界部分模糊。4例肿瘤周围有轻度至中度水肿信号。4例患者有轻度脑积水。手术中4例肿瘤可见不完整包膜。组织病理学上,所有肿瘤均见轻度核异型性,有丝分裂率为每10个高倍视野2 - 5个。结论 当脑室内或CPA肿瘤表现为多叶状实性肿块,信号略不均匀、不均匀强化明显、边界部分模糊、瘤周轻度至中度水肿或轻度脑积水时,应将APP纳入鉴别诊断。