Giannini C, Scheithauer B W, Steinberg J, Cosgrove T J
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota 55905, USA.
Neurosurgery. 1998 Dec;43(6):1478-81; discussion 1481-2. doi: 10.1097/00006123-199812000-00136.
Perineurioma, a rare benign nerve sheath neoplasm occurring in either an intraneural or soft tissue form, has never been reported to arise in the central nervous system.
We describe the clinical, radiological, and pathological features of a perineurioma arising in the choroid plexus of the third ventricle in a 65-year-old woman and causing obstructive hydrocephalus.
The lesion, apparently unassociated with a nerve, was gross totally resected by frontal craniotomy using a left-sided transcallosal approach. Short-term follow-up showed no evidence of recurrence.
Perineurioma of the variety found in soft tissue may occur in the central nervous system, wherein it shows the typical light microscopic, immunohistochemical (epithelial membrane antigen- and Collagen IV-positive, S-100 protein-negative), and ultrastructural (pinocytotic vesicles, discontinuous basement membrane) features.
神经束膜瘤是一种罕见的良性神经鞘瘤,以神经内或软组织形式出现,从未有在中枢神经系统发生的报道。
我们描述了一名65岁女性第三脑室脉络丛中发生的神经束膜瘤的临床、放射学和病理学特征,该肿瘤导致梗阻性脑积水。
该病变显然与神经无关,通过左侧经胼胝体入路的额部开颅术将其大体完全切除。短期随访未发现复发迹象。
软组织中发现的那种神经束膜瘤可能发生于中枢神经系统,在中枢神经系统中它表现出典型的光镜、免疫组化(上皮膜抗原和IV型胶原阳性,S-100蛋白阴性)及超微结构(吞饮小泡、不连续基底膜)特征。