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嗅沟孤立性神经鞘瘤:一例报告

Isolated schwannoma of the olfactory groove: a case report.

作者信息

Nascimento Luiz Augusto, Settanni Flávio Aurélio Parente, Filho José Franscisco de Góis, Sanchez Isabela Naria Dias, Cavalcante Bruna Barros, Stávale João Noberto

机构信息

Division of Skull Base Surgery, Department of Otolaryngology-Head and Neck Surgery, Universidade Federal de São Paulo, São Paulo/SP, Brazil.

Department of Head and Neck Surgery, Instituto do Cancêr Arnaldo Vieira de Carvalho, São Paulo/SP, Brazil.

出版信息

Int Arch Otorhinolaryngol. 2015 Jan;19(1):93-5. doi: 10.1055/s-0033-1353368. Epub 2013 Nov 5.

Abstract

Introduction Schwannoma of the olfactory groove is an extremely rare tumor that can share a differential diagnosis with meningioma or neuroblastoma. Objectives The authors present a case of giant schwannoma involving the anterior cranial fossa and ethmoid sinuses. Case Report The patient presented with a 30-month history of left nasal obstruction, anosmia, and sporadic ipsilateral bleeding. Computed tomography of the paranasal sinuses revealed expansive lesion on the left nasal cavity extending to nasopharynx up to ethmoid and sphenoid sinuses bilaterally with intraorbital and parasellar extension to the skull base. Magnetic resonance imaging scan confirmed the expansive tumor without dural penetration. Biopsy revealed no evidence of malignancy and probable neural cell. Bifrontal craniotomy was performed combined with lateral rhinotomy (Weber-Ferguson approach), and the lesion was totally removed. The tumor measured 8.0 × 4.3 × 3.7 cm and microscopically appeared as a schwannoma composed of interwoven bundles of elongated cells (Antoni A regions) mixed with less cellular regions (Antoni B). Immunohistochemical study stained intensively for vimentin and S-100. Conclusion Schwannomas of the olfactory groove are extremely rare, and the findings of origin of this tumor is still uncertain but recent studies point most probably to the meningeal branches of trigeminal nerve or anterior ethmoidal nerves.

摘要

引言

嗅沟神经鞘瘤是一种极其罕见的肿瘤,在鉴别诊断中可能与脑膜瘤或神经母细胞瘤混淆。目的:作者报告一例累及前颅窝和筛窦的巨大神经鞘瘤病例。病例报告:患者有30个月的左侧鼻塞、嗅觉丧失和偶发同侧鼻出血病史。鼻窦计算机断层扫描显示左侧鼻腔有占位性病变,延伸至鼻咽部,双侧累及筛窦和蝶窦,眶内及鞍旁延伸至颅底。磁共振成像扫描证实为占位性肿瘤,未穿透硬脑膜。活检未发现恶性证据,可能为神经细胞。采用双额开颅联合外侧鼻切开术(韦伯-弗格森入路),完整切除病变。肿瘤大小为8.0×4.3×3.7 cm,显微镜下表现为神经鞘瘤,由交织的细长细胞束(Antoni A区)和细胞较少的区域(Antoni B)组成。免疫组织化学研究显示波形蛋白和S-100染色强烈。结论:嗅沟神经鞘瘤极其罕见,该肿瘤的起源仍不确定,但最近的研究最有可能指向三叉神经的脑膜支或筛前神经。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e65/4392511/a6bb7cfd01de/10-1055-s-0033-1353368-i1593cr-1.jpg

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