Battal Bilal, Castillo Mauricio
Department of Radiology, University of North Carolina at Chapel Hill; Chapel Hill, North Carolina, USA - Department of Radiology, Gulhane Military Medical School; Etlik, Ankara, Turkey -
Department of Radiology, University of North Carolina at Chapel Hill; Chapel Hill, North Carolina, USA.
Neuroradiol J. 2014 Feb;27(1):55-62. doi: 10.15274/NRJ-2014-10006. Epub 2014 Feb 24.
Brain herniations into dural venous sinuses (DVS) are rare findings recently described and their etiology and clinical significance are controversial. We describe five patients with brain herniations into the DVS or calvarium identified on MRI, and discuss their imaging findings, possible causes, and relationship to the patient's symptoms. All patients were examined with MRI including high resolution pre- and post-contrast T1- and T2-weighted sequences. With respect to brain herniations we documented their locations, signal intensities in different sequences, and size. We then reviewed clinical records in an attempt to establish if any symptoms were related to the presence of these herniations. Three males and two females were examined (age range, 11-68 years). Three patients had unilateral temporal lobe herniations into transverse sinuses, one had a cerebellar herniation into the skull, and one had bilateral temporal lobe herniations into the transverse sinuses as well as a cerebellar herniation into the sigmoid sinus. In all, the herniated brain and surrounding cerebrospinal fluid (CSF) had normal signal intensity on all MRI sequences. When correlated with clinical symptoms, brain herniations were thought to be incidental and asymptomatic in three patients and two patients had histories of headaches. Brain herniations with surrounding CSF into the DVS/skull should be considered potential sources of filling defects in the DVS. We believe that they are probably incidental findings that may be more common than previously recognized and should be not confused with the more common arachnoid granulations, clots, or tumors. Two patients had headaches, but their relation to the presence of herniated brain was uncertain.
脑疝入硬脑膜静脉窦(DVS)是最近才被描述的罕见发现,其病因和临床意义存在争议。我们描述了5例在MRI上发现脑疝入DVS或颅骨的患者,并讨论了他们的影像学表现、可能的病因以及与患者症状的关系。所有患者均接受了MRI检查,包括高分辨率的增强前后T1加权和T2加权序列。关于脑疝,我们记录了它们的位置、不同序列中的信号强度以及大小。然后我们查阅了临床记录,试图确定是否有任何症状与这些脑疝的存在有关。检查了3名男性和2名女性(年龄范围为11 - 68岁)。3例患者出现单侧颞叶疝入横窦,1例小脑疝入颅骨,1例双侧颞叶疝入横窦以及小脑疝入乙状窦。总体而言,所有MRI序列上,疝入的脑组织和周围脑脊液(CSF)信号强度均正常。与临床症状相关联时,3例患者的脑疝被认为是偶然的且无症状,2例患者有头痛病史。脑疝伴周围脑脊液进入DVS/颅骨应被视为DVS中充盈缺损的潜在来源。我们认为它们可能是偶然发现,可能比之前认识到的更为常见,不应与更常见的蛛网膜颗粒、血栓或肿瘤相混淆。2例患者有头痛症状,但头痛与脑疝存在的关系尚不确定。