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Case of Orbital Mucosa-Associated Lymphoid Tissue Lymphoma Associated with Serous Retinal Detachment

机译:伴浆膜视网膜脱离的眼眶黏膜相关淋巴组织淋巴瘤1例

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摘要

We present a case of orbital mucosa-associated lymphoid tissue (MALT) lymphoma accompanied by a serous retinal detachment (SRD). A 44-year-old man who developed uveitis accompanied by a SRD in the right eye was referred to the Chiba National Hospital. B-mode ultrasonography and magnetic resonance imaging (MRI) showed a thickened choroidal membrane and a retrobulbar mass. Although topical steroid treatments improved the inflammation, the SRD did not improve. He was then referred to the Chiba University Hospital. Two months later, the retrobulbar mass had increased, and a partial resection biopsy combined with flow cytometry was performed. The final diagnosis was MALT lymphoma. After R-CHOP (rituximab–cyclophosphamide, doxorubicin, vincristine, and prednisolone) chemotherapy, signs of the tumour could not be detected and the SRD was reduced. We conclude that the SRD was most likely due to the infiltration of lymphoma cells and also to choroidal circulatory disturbances. Retrobulbar malignant lymphomas associated with a SRD are very rare and difficult to diagnosis without biopsy, but because early diagnosis is helpful in deciding the appropriate therapy, we recommend partial biopsy.
机译:我们介绍了伴有浆液性视网膜脱离(SRD)的眼眶黏膜相关淋巴样组织(MALT)淋巴瘤。一名右眼患有葡萄膜炎并伴有SRD的44岁男子被转诊至千叶国立医院。 B型超声检查和磁共振成像(MRI)显示脉络膜增厚和球后肿块。尽管局部类固醇治疗改善了炎症,但SRD并未改善。然后,他被转送到千叶大学医院。两个月后,球后肿块增加,并进行了部分切除活检和流式细胞术。最终诊断为MALT淋巴瘤。经过R-CHOP(利妥昔单抗-环磷酰胺,阿霉素,长春新碱和泼尼松龙)化疗后,无法检测到肿瘤体征,SRD降低。我们得出结论,SRD最有可能是由于淋巴瘤细胞浸润以及脉络膜循环障碍。伴有SRD的球后恶性淋巴瘤非常罕见,未经活检很难诊断,但由于早期诊断有助于确定合适的治疗方法,因此建议进行局部活检。

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