Konrad E A, Thiel H J
Ophthalmologica. 1984;188(2):118-27. doi: 10.1159/000309352.
Schwannoma of the orbit is an encapsulated, benign, noninvasive, slow-growing nerve sheath tumor which, when large enough, causes exophthalmos, optic neuropathy, diplopia, anterior orbital mass or sinusitis. An orbital schwannoma in a 84-year-old man with infiltration of the os spenoidale is reported. Schwannoma may arise anywhere within or adjacent to the orbit and is usually curable by local excision. The malignant counterpart, the malignant schwannoma, is exceedingly rare in the orbit. In orbital tumors many diagnostic steps are necessary, but the exact diagnosis is often determined only by histological examination. Schwannomas (synonyms neurilemoma, neurinoma) of the orbit are rare; they account for 1-6% of all orbital tumors. Here presented is a description of their appearance on clinical examination and on light and electron microscopy, together with a report on preoperative investigations and operative findings.
眼眶神经鞘瘤是一种有包膜的、良性的、非侵袭性的、生长缓慢的神经鞘瘤,当肿瘤足够大时,可导致眼球突出、视神经病变、复视、眶前部肿块或鼻窦炎。本文报道了1例84岁男性眼眶神经鞘瘤侵犯蝶骨的病例。神经鞘瘤可发生于眼眶内或眼眶附近的任何部位,通常通过局部切除即可治愈。其恶性对应物——恶性神经鞘瘤在眼眶中极为罕见。在眼眶肿瘤的诊断中,需要进行许多诊断步骤,但确切的诊断往往仅由组织学检查来确定。眼眶神经鞘瘤(同义词:神经膜瘤、神经瘤)很罕见,占所有眼眶肿瘤的1% - 6%。本文介绍了其临床检查、光镜及电镜下的表现,并报告了术前检查及手术所见。