Messing-Jünger A Martina, Riemenschneider Markus J, Reifenberger Guido
Brain Pathol. 2006 Jan;16(1):87-8, 93. doi: 10.1111/j.1750-3639.2006.tb00566.x.
A 21-year-old female presented with a 2-months history of tinnitus, vertigo and nausea. On magnetic resonance imaging of the brain, she demonstrated a small contrast-enhancing mass in the posterior part of the third ventricle. Intraoperatively, the tumor showed a close relationship to the choroid plexus of the third ventricle. Histopathology revealed a benign schwannoma of World Health Organization grade I. To our knowledge, only 9 cases of intraventricular Schwann cell tumors have been published so far. Most of these tumors were benign schwannomas, except for 2 cases of malignant peripheral nerve sheath tumors. The tumor of our patient is the first reported schwannoma of the third ventricle. The origin of intraventricular Schwann cell tumors is unknown. They may arise from autonomic perivascular nerves in the choroid plexus or from ectopic neural crest-derived cells. Histologically, intraventricular schwannoma needs to be distinguished from other spindle cell tumors, in particular pilocytic astrocytoma and fibroblastic meningioma.
一名21岁女性,有2个月耳鸣、眩晕和恶心病史。脑部磁共振成像显示,她在第三脑室后部有一个小的强化肿块。手术中,肿瘤显示与第三脑室脉络丛关系密切。组织病理学显示为世界卫生组织I级良性神经鞘瘤。据我们所知,迄今为止仅发表了9例脑室内施万细胞瘤病例。这些肿瘤大多数是良性神经鞘瘤,只有2例是恶性外周神经鞘膜瘤。我们患者的肿瘤是首例报道的第三脑室神经鞘瘤。脑室内施万细胞瘤的起源尚不清楚。它们可能起源于脉络丛中的自主血管周围神经,或源于异位神经嵴衍生细胞。在组织学上,脑室内神经鞘瘤需要与其他梭形细胞瘤相鉴别,尤其是毛细胞型星形细胞瘤和成纤维细胞型脑膜瘤。