Chan Leong-Perng, Wang Ling-Feng, Tai Chih-Feng, Wu Chun-Chieh, Kuo Wen-Rei
Department of Otolaryngology-Head and Neck Surgery, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Kaohsiung J Med Sci. 2009 Feb;25(2):87-92. doi: 10.1016/S1607-551X(09)70046-4.
Intranasal or paranasal sinus olfactory neuroblastoma is a rare malignant neoplasm of olfactory neuroepithelial origin, accounting for approximately 5% of paranasal sinus cancers. Most of the presenting symptoms include nasal obstruction, nasal bleeding, anosmia, rhinorrhea, and headache. In this present report, we describe a 79-year-old man who presented with bilateral nasal congestion for more than 1 year. Nasoendoscopy showed a huge, smooth, mucosal tumor in the nasopharynx with extension to the posterior nasal septum. The tumor was completely resected under endonasal endoscopy and the pathology revealed olfactory neuroblastoma. Olfactory neuroblastomas usually arise in the cribriform plate and superior turbinate. However, the origin and isolation of olfactory neuroblastomas to the sphenoid sinus is exceedingly rare. Only four cases of olfactory neuroblastoma isolated in the sphenoid sinus have been described in English literature and the frequency of presenting symptoms with cranial neuropathies and headache. We report a case of primary sphenoid sinus olfactory neuroblastoma with the greatest enlargement reported to date.
鼻内或鼻窦嗅神经母细胞瘤是一种罕见的起源于嗅神经上皮的恶性肿瘤,约占鼻窦癌的5%。大多数出现的症状包括鼻塞、鼻出血、嗅觉丧失、鼻溢液和头痛。在本报告中,我们描述了一名79岁男性,他双侧鼻塞超过1年。鼻内镜检查显示鼻咽部有一个巨大、光滑的黏膜肿瘤,延伸至后鼻中隔。该肿瘤在内镜下经鼻完全切除,病理显示为嗅神经母细胞瘤。嗅神经母细胞瘤通常起源于筛板和上鼻甲。然而,嗅神经母细胞瘤起源于蝶窦并孤立存在极为罕见。英文文献中仅描述了4例孤立于蝶窦的嗅神经母细胞瘤病例,以及伴有颅神经病变和头痛的症状出现频率。我们报告了一例原发性蝶窦嗅神经母细胞瘤,其肿大程度为迄今为止报道的最大。