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Primary hypothalamic lymphoma in a patient with systemic lupus erythematosus: case report and review of the literature.

机译:系统性红斑狼疮患者的原发性下丘脑淋巴瘤:病例报告和文献复习。

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摘要

A 67-year-old female was admitted to our department with difficulty in speech, disorientation, memory loss and seizures. Blood laboratory tests revealed diabetes insipidus. This patient had been treated with steroids for systemic lupus erythematosus (SLE) for 30 years. Due to this treatment neurological symptoms had been understated causing a long delay in performing ulterior researches. A brain MRI revealed a mass lesion in the hypothalamic area. A biopsy was performed and histopathological diagnosis was malignant large B cell lymphoma. Subsequently, she received methotrexate therapy but died of pneumonia during the second cycle. Primary central nervous system lymphoma in association with SLE is a rare occurrence but it should be considered in the diagnostic process when neurological symptoms occur. A brain MRI must be performed and corticosteroids should be interrupted. A biopsy of the cerebral mass lesion permits diagnosis and appropriate therapy may be administered.
机译:一名67岁的女性因语言,定向障碍,记忆力减退和癫痫发作而入院。血液实验室测试显示尿崩症。该患者接受类固醇激素治疗系统性红斑狼疮(SLE)30年。由于这种治疗,神经系统症状被低估了,导致进行别有用心研究的时间长了。脑部MRI显示下丘脑区域有块状病变。进行活检,组织病理学诊断为恶性大B细胞淋巴瘤。随后,她接受了甲氨蝶呤治疗,但在第二个周期死于肺炎。原发性中枢神经系统淋巴瘤伴SLE的情况很少见,但在发生神经系统症状时应在诊断过程中予以考虑。必须进行脑部MRI检查并中断皮质类固醇激素治疗。脑块病变的活检可以诊断并可以进行适当的治疗。

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