Rosso Dominic, Lee Donald H, Ferguson Gary G, Tailor Chetna, Iskander Sam, Hammond Robert R
Department of Clinical Neurological Sciences, London Health Sciences Centre, University of Western Ontario, London, ON, Canada.
Can J Neurol Sci. 2003 Aug;30(3):272-7. doi: 10.1017/s0317167100002730.
Dural cavernous angiomas are uncommon benign vascular malformations which may present intraoperative difficulties in hemostasis when the diagnosis is not suspected preoperatively. Preoperative diagnosis can be difficult when angiomas show atypical features and share imaging characteristics with other entities.
A patient presented with a radiographically aggressive lesion, subsequently identified as a dural cavernous angioma. The lesion is reviewed and its clinical, radiographic, and pathological features are compared with other vascular malformations.
A 40-year-old man presented with new onset seizures and an enhancing lesion infiltrating the floor of the right middle cranial fossa. Due to its aggressive radiographic appearance, initial considerations included chondrosarcoma, meningioma or metastasis. Pathological examination, however, revealed the lesion to be a cavernous angioma of dura.
This uncommon lesion may present a diagnostic challenge with significant intraoperative implications. T2 sequence hyperintensity in a relevant lesion should raise suspicion of an hemangioma. It is important to be aware of this entity and its potential to mimic other entities on radiographic grounds.
硬脑膜海绵状血管瘤是罕见的良性血管畸形,若术前未怀疑其诊断,术中止血可能会遇到困难。当血管瘤表现出非典型特征并与其他病变具有相同的影像学特征时,术前诊断可能会很困难。
一名患者出现影像学上具有侵袭性的病变,随后被确诊为硬脑膜海绵状血管瘤。对该病变进行回顾,并将其临床、影像学和病理特征与其他血管畸形进行比较。
一名40岁男性出现新发癫痫,并有一个强化病变浸润右侧中颅窝底部。由于其影像学表现具有侵袭性,最初考虑为软骨肉瘤、脑膜瘤或转移瘤。然而,病理检查显示该病变为硬脑膜海绵状血管瘤。
这种罕见的病变可能带来诊断挑战,并对术中情况有重大影响。相关病变在T2序列上呈高信号应引起对血管瘤的怀疑。了解这一病变及其在影像学上模仿其他病变的可能性很重要。