Fujii Takashi, Otani Naoki, Doi Kazuma, Miyama Masataka, Otsuka Yohei, Matsumoto Takashi, Yoshiura Toru, Takeuchi Satoru, Tomura Satoshi, Tomiyama Arata, Toyooka Terushige, Wada Kojiro, Mori Kentaro
Department of Neurosurgery, National Defense Medical College.
No Shinkei Geka. 2017 Oct;45(10):919-928. doi: 10.11477/mf.1436203618.
Schwannomas originating from the olfactory nerve are extremely rare because the olfactory nerve does not normally contain Schwann cells. We describe a case of a giant schwannoma of the olfactory groove. A 73-year-old woman presented with anosmia persisting for 10 months. Head computed tomography(CT)for head trauma at another hospital demonstrated a tumor lesion located in the left frontal lobe and paranasal sinus. She had never suffered epilepsy, and past medical history and family history identified no indicators. Neurological examination revealed anosmia and dementia. Head CT demonstrated a tumor lesion with bone erosion, causing a defect of about 5cm in the frontal base. Head magnetic resonance(MR)imaging with contrast medium indicated a lesion that was 6cm in diameter, with heterogeneous enhancement and severe perifocal edema in the left frontal base, extending into the paranasal cavity. The tumor was resected through a left extradural subfrontal approach with bicoronal frontal craniotomy. The endoscopic approach was also performed simultaneously to remove the tumor in the paranasal sinus. The cystic tumor was soft and easy to bleed. Intraoperatively the right olfactory nerve was confirmed, but the left olfactory nerve could not be identified because of replacement by the tumor, suggesting that the tumor had originated from the left olfactory nerve. The defect of the dura was repaired with femoral fascia, the pedunculated periosteal flap was laid over the frontal base, and the bone defect was repaired with the inner plate of the frontal calvaria. Postoperative head MR imaging with contrast medium revealed no residual lesion. The patient was discharged 25 days after surgery, without new neurological deficits. Histological examination identified mixed Antoni type A and Antoni type B schwannoma on hematoxylin and eosin staining and S-100 protein on immunostaining.
起源于嗅神经的施万细胞瘤极为罕见,因为嗅神经通常不含施万细胞。我们报告一例嗅沟巨大施万细胞瘤病例。一名73岁女性,嗅觉缺失持续10个月。在另一家医院因头部外伤行头颅计算机断层扫描(CT)显示左额叶和鼻窦有肿瘤病变。她从未患过癫痫,既往病史和家族史均未发现相关指征。神经系统检查发现嗅觉缺失和痴呆。头颅CT显示肿瘤病变伴有骨质侵蚀,导致额底部约5cm的缺损。头颅磁共振(MR)增强成像显示左侧额底部有一个直径6cm的病变,强化不均匀,灶周重度水肿,并延伸至鼻腔。通过左侧硬膜外额下入路联合双冠状额部开颅术切除肿瘤。同时采用内镜入路切除鼻窦内的肿瘤。囊性肿瘤质地柔软,容易出血。术中确认右侧嗅神经,但左侧嗅神经因被肿瘤取代而无法辨认,提示肿瘤起源于左侧嗅神经。硬脑膜缺损用股筋膜修复,带蒂骨膜瓣覆盖在额底部,颅骨缺损用额骨内板修复。术后头颅MR增强成像显示无残留病变。患者术后25天出院,无新的神经功能缺损。苏木精-伊红染色及免疫染色S-100蛋白显示组织学检查为混合型Antoni A型和Antoni B型施万细胞瘤。