Partial Oculomotor Nerve Palsy as the First Presentation of Extranodal Natural Killer/T-Cell Lymphoma.

IF 0.9 Journal of medical cases Pub Date : 2025-02-01 Epub Date: 2025-01-25 DOI:10.14740/jmc5092
Worapot Srimanan, Phawasutthi Keokajee
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Abstract

Extranodal natural killer/T-cell lymphoma (ENKTL) is a rare and aggressive subtype of non-Hodgkin lymphoma, typically involving the nasal cavity. However, it can occasionally present in extranodal sites without nasal involvement, complicating diagnosis. This report describes a 78-year-old man who presented with progressive double vision and visual loss in the right eye over 3 weeks. Examination revealed partial oculomotor nerve palsy with pupillary involvement and signs of optic neuropathy, leading to a diagnosis of orbital apex syndrome. The nasopharyngeal evaluation showed no nasal lesions. Magnetic resonance imaging (MRI) identified diffuse enhancement of the extraocular muscles, intraorbital soft tissues, and optic nerve sheath in the right orbit. A right medial rectus muscle biopsy confirmed extranodal NK/T-cell lymphoma through immunohistochemical analysis. Chemotherapy was initiated, significantly improving both ophthalmoplegia and visual acuity. This case underscores the importance of comprehensive neuro-ophthalmic evaluation and biopsy for diagnosing ENKTL, especially in atypical presentations without nasal involvement. Early detection and treatment are critical for achieving favorable outcomes in this rare disease.

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部分动眼神经麻痹是结外自然杀伤/ t细胞淋巴瘤的第一表现。
结外自然杀伤/ t细胞淋巴瘤(ENKTL)是一种罕见的侵袭性非霍奇金淋巴瘤亚型,通常累及鼻腔。然而,它偶尔可以出现在结外部位而不累及鼻腔,使诊断复杂化。本报告描述一位78岁男性,在3周内出现进行性双重视力和右眼视力丧失。检查显示部分动眼神经麻痹伴瞳孔受累及视神经病变征象,诊断为眶尖综合征。鼻咽部检查未见鼻部病变。磁共振成像(MRI)发现右眼眶眼外肌、眶内软组织和视神经鞘弥漫性增强。通过免疫组织化学分析,右内侧直肌活检证实结外NK/ t细胞淋巴瘤。化疗开始后,眼瘫和视力均有明显改善。本病例强调了综合神经眼科评估和活检诊断ENKTL的重要性,特别是在没有鼻腔受累的非典型表现中。早期发现和治疗对于实现这种罕见疾病的良好结果至关重要。
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