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以突发单侧失明为表现的嗅神经母细胞瘤。视神经脱髓鞘的组织病理学证实。

Esthesioneuroblastoma presenting as sudden unilateral blindness. Histopathologic confirmation of optic nerve demyelination.

作者信息

Berman E L, Chu A, Wirtschafter J D, Cameron J D, Manivel J C, Duvall A J, Haines S J

机构信息

Department of Ophthalmology, University of Minnesota School of Medicine, Minneapolis.

出版信息

J Clin Neuroophthalmol. 1992 Mar;12(1):31-6.

PMID:1532598
Abstract

We report here a case of esthesioneuroblastoma an 11-year-old girl presenting as acute loss of vision with minimal evidence of orbital, nasal, or paranasal sinus disease, a rare presenting symptom for this tumor. The initial diagnosis was postviral optic neuritis, a pattern of presentation not previously reported. When vision failed to improve, magnetic resonance imaging revealed a lesion in the posterior ethmoid and sphenoid sinuses. After a biopsy, the tumor was excised through the cranium and paranasal sinuses. A mass completely surrounding the optic nerve without invasion was found. Histochemical staining suggested demyelination secondary to compression, confirming the clinical impression of optic neuritis. Anti-Leu 7 monoclonal antibody is useful in characterizing of this tumor, since other immunochemical stains can be misleading. Radiation and chemotherapy were given after the tumor was removed. Two years later, the patient has had neither recurrence nor complications.

摘要

我们在此报告一例嗅神经母细胞瘤病例,患者为一名11岁女孩,表现为急性视力丧失,眼眶、鼻腔或鼻窦疾病迹象极少,这是该肿瘤罕见的表现症状。初步诊断为病毒性后视神经炎,此前未见这种表现形式的报道。当视力未改善时,磁共振成像显示筛窦后部和蝶窦有病变。活检后,通过颅骨和鼻窦切除肿瘤。发现一个完全包围视神经且无侵犯的肿块。组织化学染色提示为压迫继发的脱髓鞘,证实了视神经炎的临床印象。抗Leu 7单克隆抗体有助于该肿瘤的特征化诊断,因为其他免疫化学染色可能会产生误导。肿瘤切除后给予放疗和化疗。两年后,患者既无复发也无并发症。

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