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眼葡萄膜原发性结外边缘区淋巴瘤伴弥漫性广泛眶内蔓延及视神经和脑膜局限性浸润,临床表现为伪装综合征的葡萄膜炎:一例报告。

Primary extranodal marginal zone lymphoma of the uvea associated with massive diffuse epibulbar extension and focal infiltration of the optic nerve and meninges, clinically presented as uveitis masquerade syndrome: a case report.

机构信息

Institute of Ophthalmology, Clinical Centre of Serbia, Pasterova 2, Belgrade, 11000, Serbia.

出版信息

Med Oncol. 2010 Sep;27(3):1010-6. doi: 10.1007/s12032-009-9325-6. Epub 2009 Oct 9.

Abstract

To report a clinical, histopathological and immunohistochemical findings in a case of primary extranodal marginal zone lymphoma of the uvea associated with massive diffuse extraocular episcleral extension and focal infiltration of the optic nerve and meninges, clinically presented as longstanding uveitis masquerade syndrome. Interventional case reports with histopathological correlation. We describe a 80-year-old male patient with a 3-year history of chronic recurrent hypertensive (pan) uveitis associated with ocular pain, unresponsive to topical and systemic anti-inflammatory, immunosuppressive, antibiotic/antiviral and antiglaucomatous therapy. Because the eye was not salvageable with conservative treatment, enucleation of blind and painful eye was performed. Findings from histopathological and immunohistochemistry examination of the enucleated eye showed an extranodal marginal zone lymphoma of the uveal tract with massive epibulbar extension and optic nerve and meningeal penetration. During almost 3 years of clinical course and 6 months after the enucleation, there were no systemic manifestations of lymphoma, and patient has not required subsequent treatment. Primary lymphoproliferative lesions of the uvea, comprising the iris, ciliary body and choroid are very rare, associated with epibulbar extension extremely and with optic nerve and menigeal penetration exceptionally. Despite its rarity, primary lymphoma of the uvea should be included in the differential diagnosis particularly in older patients with longstanding recurrent uveitis.

摘要

报告 1 例眼葡萄膜原发性结外边缘区淋巴瘤,伴有巨大弥漫性眼球前段巩膜外扩展和视神经及脑膜局灶性浸润,临床上表现为长期葡萄膜炎伪装综合征。伴有组织病理学相关性的介入性病例报告。我们描述了 1 例 80 岁男性患者,有 3 年慢性复发性高血压(全)葡萄膜炎病史,伴有眼部疼痛,对局部和全身抗炎、免疫抑制、抗生素/抗病毒和抗青光眼治疗无反应。由于保守治疗无法挽救眼球,对失明和疼痛的眼球进行了眼球摘除术。对眼球摘除物的组织病理学和免疫组织化学检查结果显示,眼葡萄膜存在结外边缘区淋巴瘤,伴有巨大的眼球前段巩膜外扩展和视神经及脑膜浸润。在近 3 年的临床病程和眼球摘除术后 6 个月内,患者没有出现淋巴瘤的全身表现,也不需要后续治疗。虹膜、睫状体和脉络膜组成的眼葡萄膜原发性淋巴增生性病变非常罕见,与前段巩膜外扩展有关,与视神经和脑膜浸润有关。尽管罕见,但原发性眼葡萄膜淋巴瘤应特别纳入长期复发性葡萄膜炎老年患者的鉴别诊断中。

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