Patel Nitesh P, Robinson Timothy M, Lesley Walter S, Garrett David, Shan Yuan, Huang Jason H
Texas A&M College of Medicine, Temple, Texas, USA.
Texas A&M College of Medicine, Temple, Texas, USA; Department of Neurosurgery, Baylor Scott and White Health, Temple, Texas, USA.
World Neurosurg. 2019 Feb;122:165-170. doi: 10.1016/j.wneu.2018.10.188. Epub 2018 Nov 4.
Hemangioblastomas (HBMs) are benign vascular neoplasms that most commonly arise within the cerebellum. Although other vascular lesions should be considered in the differential diagnosis, HBMs rarely resemble aneurysms on neuroimaging and only 1 case of a cerebellar HBM mimicking a posterior fossa aneurysm has been reported. Here we describe a retromedullary HBM that masqueraded as a distal posterior inferior cerebellar artery (PICA) medullary branch aneurysm.
A 63-year-old asymptomatic male was incidentally diagnosed with an unruptured 3-mm left PICA aneurysm via computed tomography angiography during a workup for carotid stenosis. Two years later, the presumed aneurysm enlarged to 6.5 mm and prompted elective treatment. Endovascular treatment was unsuccessful, and the patient was immediately transitioned to a craniotomy for aneurysm clipping. After microsurgical dissection, the lesion was visualized on the posterior medullary surface with several small arterial feeders extending from the brainstem into the aneurysm dome, but no major parent vessel was observed. Because a clip could not be safely applied to these small vessels, they were instead coagulated and the lesion was completely resected. Final pathology revealed hemangioblastoma (World Health Organization grade I).
To our knowledge, this is the second case of HBM mimicking a PICA aneurysm. Given the rarity of PICA medullary branch aneurysms and their highly symptomatic nature, other etiologies, especially HBM, should be strongly considered when an apparent distal PICA aneurysm is diagnosed in an asymptomatic patient. If the lesion is unamenable to endovascular treatment, there should be high suspicion for HBM and subsequent craniotomy should be pursued.
血管母细胞瘤(HBMs)是一种良性血管肿瘤,最常见于小脑。尽管在鉴别诊断中应考虑其他血管病变,但HBMs在神经影像学上很少类似动脉瘤,仅有1例小脑HBMs模仿后颅窝动脉瘤的病例报道。在此,我们描述1例延髓后HBMs,其伪装成小脑后下动脉(PICA)延髓分支远端动脉瘤。
一名63岁无症状男性在因颈动脉狭窄进行检查时,通过计算机断层血管造影偶然诊断出一个未破裂的3mm左PICA动脉瘤。两年后,推测的动脉瘤增大至6.5mm并促使进行择期治疗。血管内治疗未成功,患者立即转为开颅夹闭动脉瘤。显微手术解剖后,在延髓后表面可见病变,有几条小动脉分支从脑干延伸至动脉瘤瘤体,但未观察到主要供血血管。由于无法安全地对这些小血管夹闭,改为对其进行凝固,病变被完全切除。最终病理显示为血管母细胞瘤(世界卫生组织I级)。
据我们所知,这是第二例HBMs模仿PICA动脉瘤的病例。鉴于PICA延髓分支动脉瘤罕见且症状严重,当在无症状患者中诊断出明显的PICA远端动脉瘤时,应强烈考虑其他病因,尤其是HBMs。如果病变无法进行血管内治疗,应高度怀疑HBMs,并随后进行开颅手术。