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Retrospective cytological study of intraocular lymphoma using vitreous and intraocular perfusion fluid

机译:玻璃体和眼内灌注液对眼内淋巴瘤的回顾性细胞学研究

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摘要

Intraocular lymphoma (IOL) is an extremely rare tumor. We carried out a retrospective cytopathological study with vitreous and intraocular perfusion fluid obtained on conducting a pars plana vitrectomy in 18 cases of IOL. In the 18 cases, nine were patients of Kansai Medical University Takii Hospital from 1991 to 2007, and the other nine had already been reported by other hospitals. Most patients were male, and the average age at onset was 60.4-year-old. The main symptoms were vitreous opacity, amblyopia, and blurred vision. Cases of primary intraocular lymphoma numbered 8/15 (53%), while cases of infiltration of malignant lymphoma from the brain numbered 2/15 (13%). Although IOL contains various subtypes of lymphoma, the most frequent subtype is diffuse large B-cell type lymphoma. It has been reported that making a definite diagnosis of IOL is difficult because the clinical symptoms and examinations are similar to chronic uveitis, and so IOL is called "masquerade syndrome." Recently, serological and molecular pathological studies have been carried out in addition to morphological examination. However, a cytological diagnosis based on the clinical background and/or image findings is important for the diagnosis of IOL, because of the volume limit of the vitreous fluid and difficulty of obtaining specimens from the inside of the eyes.
机译:眼内淋巴瘤(IOL)是一种极为罕见的肿瘤。我们对18例IOL进行了玻璃体玻璃体切除术时获得的玻璃体和眼内灌注液进行了回顾性细胞病理学研究。在这18例病例中,有9例是1991年至2007年的关西医科大学T木医院,其他9例已经由其他医院报告。大多数患者为男性,平均发病年龄为60.4岁。主要症状是玻璃体混浊,弱视和视力模糊。原发性眼内淋巴瘤病例为8/15(53%),而脑部浸润性恶性淋巴瘤病例为2/15(13%)。尽管IOL包含多种淋巴瘤亚型,但最常见的亚型是弥漫性大B细胞型淋巴瘤。据报道,由于临床症状和检查类似于慢性葡萄膜炎,很难对IOL进行明确诊断,因此IOL被称为“化装舞会综合症”。最近,除了形态学检查之外,还进行了血清学和分子病理学研究。然而,由于玻璃体液的体积限制以及难以从眼内获取标本,因此基于临床背景和/或图像发现的细胞学诊断对于IOL的诊断很重要。

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