Suppr超能文献

在免疫功能正常的患者中表现为原发性中枢神经系统恶性肿瘤的进行性多灶性白质脑病。

Progressive Multifocal Leukoencephalopathy Presenting as Primary CNS Malignancy in an Immunocompetent Patient.

作者信息

Truong Rachel D, Vadlapatla Vamshi K, Avgeropoulos Nicholas G

机构信息

Department of Internal Medicine, Orlando Regional Medical Center, Orlando, USA.

Department of Hematology and Medical Oncology, Orlando Regional Medical Center, Orlando, USA.

出版信息

Cureus. 2023 Sep 23;15(9):e45815. doi: 10.7759/cureus.45815. eCollection 2023 Sep.

Abstract

Progressive multifocal leukoencephalopathy (PML) is an infection caused by the John Cunningham virus (JCV), usually in an immunocompromised host. We present the case of a 74-year-old male who presented with a six-week history of progressive memory loss, episodic confusion, and aphasia. Cranial nerve, motor, sensory, and coordination testing were unremarkable. Magnetic resonance imaging (MRI) of the brain and spectroscopy were concerning for primary CNS lymphoma vs. diffuse glioma. Microscopic examination after the patient underwent left frontal stereotactic brain biopsy was suggestive of a viral infection, and further testing with JCV DNA in-situ hybridization (ISH) confirmed the diagnosis of PML. The patient's condition started resolving without treatment. This case demonstrates, to our knowledge, the first known case of primary PML masquerading as CNS lymphoma in modern literature.

摘要

进行性多灶性白质脑病(PML)是由约翰·坎宁安病毒(JCV)引起的一种感染,通常发生在免疫功能低下的宿主中。我们报告一例74岁男性患者,其有六周进行性记忆力减退、发作性意识模糊和失语的病史。颅神经、运动、感觉和协调测试均无异常。脑部磁共振成像(MRI)和光谱检查提示原发性中枢神经系统淋巴瘤与弥漫性胶质瘤。患者接受左额叶立体定向脑活检后的显微镜检查提示病毒感染,进一步的JCV DNA原位杂交(ISH)检测确诊为PML。患者的病情未经治疗开始缓解。据我们所知,该病例是现代文献中首例伪装成中枢神经系统淋巴瘤的原发性PML病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e13/10591460/ac4610a46a07/cureus-0015-00000045815-i01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验