Tian Wei-Zhong, Yu Xiang-Rong, Wang Wei-Wei, Zhang B O, Xia Jian-Guo, Liu Han-Qiu
Department of Radiology, Taizhou People's Hospital, Taizhou, Jiangsu 225300, P.R. China.
Department of Radiology, Zhuhai People's Hospital, Jinan University, Zhuhai, Guangdong 519000, P.R. China.
Oncol Lett. 2016 May;11(5):3105-3110. doi: 10.3892/ol.2016.4356. Epub 2016 Mar 21.
The current study aimed to present the neuroradiological and histopathological features of intracranial hemangioendothelioma (HE). The computed tomography (CT; n=3) and magnetic resonance imaging (MRI; n=7) features, and the clinical presentations of 7 patients with pathologically documented HEs were retrospectively analyzed. Lesions were observed in the right side of the skull (the frontal bone in 1 patient and the parietal bone in 1 patient), the tentorium (2 patients), the cerebral falx (1 patient), the right cavernous sinus (1 patient) and the right temporal lobe (1 patient). The tumor was lobulated in 5 cases and round in 2 cases. The majority of tumors appeared isointense or hypointense with multiple scattered hyperintensities on T1-weighted MRI. Moreover, the lesions appeared as inhomogeneous hyperintense regions with multiple enlarged and tortuous blood flow voids on T2-weighted MRI. The lesions also showed marked gadolinium enhancement in a honeycomb pattern. CT scan results showed a isoattenuation region (32-47 HU), with numerous small, round, high-density foci. The 2 cases with skull lesions presented with local bone destruction and discontinuous bone lines of the tabula interna ossis cranii. In 1 case, MR angiography revealed abnormal vessels in the basilar region. A total of 4 cases were epithelial HE, 2 were retiform HE and 1 was kaposiform HE. Histological examination revealed endothelial cell proliferation with vascular lesions and a mucous matrix or dense fibrous mesenchyme. In conclusion, intracranial HE is rare, but should be considered in the differential diagnosis when evaluating intracranial neoplasms. A well-defined lobulated mass and imaging features that include internal heterogeneity, small scattered hemorrhages and thromboses, signal voids of vessels, and marked and delayed enhancement may confirm the diagnosis of HE.
本研究旨在呈现颅内血管内皮瘤(HE)的神经放射学和组织病理学特征。回顾性分析了7例经病理证实的HE患者的计算机断层扫描(CT;n = 3)和磁共振成像(MRI;n = 7)特征及临床表现。病变见于颅骨右侧(1例位于额骨,1例位于顶骨)、小脑幕(2例)、大脑镰(1例)、右侧海绵窦(1例)和右侧颞叶(1例)。肿瘤呈分叶状5例,圆形2例。大多数肿瘤在T1加权MRI上呈等信号或低信号,伴有多个散在的高信号。此外,病变在T2加权MRI上表现为不均匀的高信号区,伴有多个扩大和迂曲的血流空洞。病变还显示出蜂窝状的明显钆增强。CT扫描结果显示等密度区(32 - 47 HU),有许多小的圆形高密度灶。2例颅骨病变患者出现局部骨质破坏和颅骨内板骨线中断。1例患者磁共振血管造影显示基底区域血管异常。共有4例为上皮样HE,2例为网状HE,1例为卡波西样HE。组织学检查显示内皮细胞增生伴血管病变及黏液基质或致密纤维间质。总之,颅内HE罕见,但在评估颅内肿瘤时应考虑其在鉴别诊断中的可能性。边界清晰的分叶状肿块以及包括内部异质性、小的散在出血和血栓形成、血管信号空洞以及明显和延迟增强在内的影像学特征可能有助于确诊HE。