Orbital apex syndrome secondary to sinonasal diffuse large B cell lymphoma: how rare is it?

See-Teng Tan, Nor Binti Tak Akmar, P. Sudha
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Abstract

A sinonasal lymphoma is an uncommon form of non-Hodgkin lymphoma (NHL), comprising only 1.5% of all lymphomas. We report a rare case of primary sinonasal diffuse large B cell lymphoma (DLBCL) found accompanying orbital apex syndrome. A 75-year-old Chinese man presented with progressively reduced visualacuity in the left eye for over 2 months and frequent rhinorrhoea for the previous 4 months. Upon examination, his left eye was noted with poor vision with incomplete ptosis, periorbital fullness, and ophthalmoplegia. Computed tomography scan of the brain and orbit showed nasal soft tissue mass with local extension to the left extraconal space. Histopathological examination of the nasal biopsy tissue showed high-grade DLBCL. The distal cranial neuropathy caused by the lymphomatous infiltration of the left paranasal sinuses had preceded the systemic manifestation. The patient was initiated on chemotherapy and has been, at the time of writing, in remission for 8 months after presentation.
鼻窦弥漫性大B细胞淋巴瘤继发的眶尖综合征:有多罕见?
鼻窦淋巴瘤是一种罕见的非霍奇金淋巴瘤(NHL),仅占所有淋巴瘤的1.5%。我们报告一例罕见的原发性鼻窦弥漫性大B细胞淋巴瘤(DLBCL)并发眶尖综合征。一位75岁的中国男性,左眼视力逐渐下降超过2个月,前4个月频繁流鼻水。经检查,左眼视力不佳,有不完全性上睑下垂、眶周充盈及眼麻痹。脑部及眶部电脑断层扫描显示鼻软组织肿块局部延伸至左外腔。鼻活检组织病理检查显示高级别DLBCL。由左鼻窦淋巴瘤浸润引起的远端颅神经病变先于全身表现。患者开始化疗,在撰写本文时,病情缓解期为8个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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