Bifocal optic and facial nerve t-cell lymphoma.

A Van Hoey, A Shah, J De Zaeytijd, C Van Den Broecke, C Decock, B P Leroy
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Abstract

Purpose: Optic nerve and optic nerve sheath infiltration by a systemic lymphoma is uncommon, but is exceedingly rare when caused by a T-cell lymphoma. This then generally occurs in association with central nervous system (CNS) involvement. We report on a rare case of optic and facial nerve T-cell lymphoma infiltration, without CNS involvement.

Methods: A 63-year old female with systemic T-cell lymphoma in clinical remission presented with painful loss of vision in the left eye. She was initially treated for presumed recurrent optic neuritis. A thorough clinical work-up was performed, followed by an optic nerve biopsy with histopathology.

Results: There was no perception of light in the left eye, with a marked relative afferent pupillary defect. Fundoscopy showed significant optic disc oedema and a large peripapillary subretinal infiltration. Subsequently, she developed a 7th cranial nerve paresis. Cranial MRI showed thickening and contrast enhancement of the left optic nerve and right facial nerve. Optic nerve biopsy showed infiltration of CD3- and CD5- positive lymphocytes. A complete systemic workup revealed no evidence of disease elsewhere. The patient was thus considered to have bifocal cranial recurrence of T-cell lymphoma, for which radiotherapy was started.

Conclusions: Optic nerve infiltration from systemic lymphoma is rare and generally occurs with CNS involvement. A bifocal pattern of recurrence from systemic T-cell lymphoma involving the right facial nerve and left optic nerve was seen in this patient. A review of the literature highlights the highly atypical nature of this presentation.

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双焦点视神经和面神经t细胞淋巴瘤。
目的:视神经及视神经鞘浸润的系统性淋巴瘤是罕见的,但当引起t细胞淋巴瘤是极其罕见的。这通常与中枢神经系统(CNS)受累有关。我们报告一例罕见的视神经和面神经t细胞淋巴瘤浸润,没有中枢神经受累。方法:63岁女性,全身性t细胞淋巴瘤,临床缓解,表现为左眼疼痛性视力丧失。她最初因假定复发性视神经炎而接受治疗。进行了彻底的临床检查,随后进行了视神经活检和组织病理学检查。结果:左眼无光感,瞳孔相对传入缺损明显。眼底镜检查显示明显视盘水肿和大的乳头周围视网膜下浸润。随后,她出现了第7脑神经麻痹。颅脑MRI显示左侧视神经和右侧面神经增厚和增强。视神经活检显示CD3和CD5阳性淋巴细胞浸润。一个完整的系统检查没有发现其他疾病的证据。因此,该患者被认为是双灶性脑t细胞淋巴瘤复发,并开始放疗。结论:系统性淋巴瘤的视神经浸润是罕见的,通常累及中枢神经系统。本病例为双焦点型系统性t细胞淋巴瘤复发,累及右侧面神经和左侧视神经。对文献的回顾强调了这种表现的高度非典型性质。
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