Carangelo Biagio R, Muscas Giovanni, Miracco Clelia, Muzii Vitaliano F
Department of Neurological and Sensory Sciences, Division of Neurosurgery, Siena University Hospital, Siena, Italy.
Department of Medicine, Surgery, and Neurosciences, Section of Neurosurgery, University of Siena, Siena, Italy.
Surg Neurol Int. 2017 May 26;8:94. doi: 10.4103/2152-7806.207115. eCollection 2017.
Some glial tumors have been observed in association with different types of vascular malformations of the brain (angiogliomas). However, the association of ganglioglioma with other vascular malformations is extremely rare, with only few cases reported in the literature, one of which is referred to as "angioganglioglioma."
Two patients presented with acute onset of neurological symptoms, with magnetic resonance imaging (MRI) finding of cavernoma of the left middle cerebellar penduncle, and small mass of the chiasmatic region, respectively. After microsurgical excision, histopathological examination revealed mixed ganglioglioma and cavernous malformation in both cases. Postoperative course was uneventful, and follow-up MRI showed complete removal of the tumor with no recurrence after 4 years.
Angiogliomas are very uncommon tumors. In literature, we found different interpretations of such lesions, although they should most probably be considered as distinct pathological entities. Although the association of ganglioglioma with cavernoma is extremely rare, it could be considered as a most peculiar form of angioglioma, and supports the existence of angioganglioglioma.
一些胶质肿瘤已被观察到与不同类型的脑血管畸形(血管胶质瘤)相关。然而,神经节胶质瘤与其他血管畸形的关联极为罕见,文献中仅报道了少数病例,其中之一被称为“血管神经节胶质瘤”。
两名患者均急性起病出现神经症状,磁共振成像(MRI)分别发现左小脑中间脚海绵状血管瘤和视交叉区小肿块。显微手术切除后,组织病理学检查显示两例均为混合性神经节胶质瘤和海绵状畸形。术后病程顺利,随访MRI显示肿瘤完全切除,4年后无复发。
血管胶质瘤是非常罕见的肿瘤。在文献中,我们发现对这类病变有不同的解释,尽管它们很可能应被视为不同的病理实体。虽然神经节胶质瘤与海绵状血管瘤的关联极为罕见,但可将其视为血管胶质瘤的一种极为特殊的形式,并支持血管神经节胶质瘤的存在。