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一名年轻男性因鼻窦未分化癌继发压迫性视神经病变

Compressive Optic Neuropathy Secondary to Sinonasal Undifferentiated Carcinoma in a Young Male.

作者信息

Hassan Maizatul Nadia, Wan Hitam Wan Hazabbah, Masnon Nurul Ain, Govindasamy Subash, Omar Ahmad Razif

机构信息

Department of Ophthalmology and Visual Science, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, MYS.

Department of Ophthalmology, 96 Malaysian Armed Forces Hospital, Royal Malaysian Navy Base, Lumut, MYS.

出版信息

Cureus. 2021 Oct 25;13(10):e19042. doi: 10.7759/cureus.19042. eCollection 2021 Oct.

Abstract

Sinonasal undifferentiated carcinoma (SNUC) is an extremely aggressive malignancy. Extension to the orbit and adjacent structures is common, but isolated visual loss as a presenting symptom is rare. We report a rare case of SNUC with bilateral visual loss as the initial manifestation. A 34-year-old gentleman was presented with acute onset loss of vision in both eyes for one week. It was followed by recurrent headaches and epistaxis. Visual acuity in the right eye was 2/60 and 3/60 in the left eye. Funduscopy showed a bilateral swollen disc. Neuroimaging revealed a large mass in the ethmoidal sinus extended laterally causing compression to recti muscles and the optic nerves. The histopathological examination of nasal tissue biopsy showed features of SNUC with bone and perineural invasion. A diagnosis of SNUC with bilateral compressive optic neuropathy was established. The patient underwent tumor debulking and base of skull reconstruction by the neurosurgical team. This was then followed by chemotherapy and radiotherapy. The patient's right eye visual acuity initially improved to 6/9. However, his both eye vision developed into no light perception during treatment. In conclusion, SNUC is a highly aggressive tumor that may present with acute blindness. Early treatment may save a life, but the visual prognosis is guarded due to extensive optic nerve damage caused by tumor compression.

摘要

鼻窦未分化癌(SNUC)是一种极具侵袭性的恶性肿瘤。肿瘤延伸至眼眶及相邻结构很常见,但以孤立性视力丧失作为首发症状则较为罕见。我们报告一例罕见的以双侧视力丧失为初始表现的鼻窦未分化癌病例。一名34岁男性患者因双眼急性视力丧失一周前来就诊。随后出现反复头痛和鼻出血。右眼视力为2/60,左眼视力为3/60。眼底检查显示双侧视盘水肿。神经影像学检查发现筛窦有一个大肿块,向外侧延伸,压迫直肌和视神经。鼻组织活检的组织病理学检查显示为鼻窦未分化癌,伴有骨质和神经周围浸润。确诊为鼻窦未分化癌伴双侧压迫性视神经病变。患者接受了神经外科团队进行的肿瘤减瘤和颅底重建手术。随后进行了化疗和放疗。患者右眼视力最初改善至6/9。然而,在治疗过程中他的双眼视力发展为无光感。总之,鼻窦未分化癌是一种高度侵袭性的肿瘤,可能表现为急性失明。早期治疗可能挽救生命,但由于肿瘤压迫导致广泛的视神经损伤,视力预后不容乐观。

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