Differential diagnosis of Jakob-Creutzfeldt disease.

Ross W Paterson, Charles C Torres-Chae, Amy L Kuo, Tim Ando, Elizabeth A Nguyen, Katherine Wong, Stephen J DeArmond, Aissa Haman, Paul Garcia, David Y Johnson, Bruce L Miller, Michael D Geschwind
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引用次数: 80

Abstract

Objectives: To identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) during the course of their disease and determine which medical specialties saw patients with sCJD prior to the correct diagnosis being made and at what point in the disease course a correct diagnosis was made.

Design: Retrospective medical record review.

Setting: A specialty referral center of a tertiary academic medical center.

Participants: One hundred sixty-three serial patients over a 5.5-year period who ultimately had pathologically proven sCJD. The study used the subset of 97 patients for whom we had adequate medical records.

Main outcome measures: Other diagnoses considered in the differential diagnosis and types of medical specialties assessing patients with sCJD.

Results: Ninety-seven subjects' records were used in the final analysis. The most common disease categories of misdiagnosis were neurodegenerative, autoimmune/paraneoplastic, infectious, and toxic/metabolic disorders. The most common individual misdiagnoses were viral encephalitis, paraneoplastic disorder, depression, vertigo, Alzheimer disease, stroke, unspecified dementia, central nervous system vasculitis, peripheral neuropathy, and Hashimoto encephalopathy. The physicians who most commonly made these misdiagnoses were primary care physicians and neurologists; in the 18% of patients who were diagnosed correctly at their first assessment, the diagnosis was almost always by a neurologist. The mean time from onset to diagnosis was 7.9 months, an average of two-thirds of the way through their disease course.

Conclusions: Diagnosis of sCJD is quite delayed. When evaluating patients with rapidly progressive dementia with suspected neurodegenerative, autoimmune, infectious, or toxic/metabolic etiology, sCJD should also be included in the differential diagnosis, and appropriate diagnostic tests, such as diffusion brain magnetic resonance imaging, should be considered. Primary care physicians and neurologists need improved training in sCJD diagnosis.

Abstract Image

雅各布-克雅氏病的鉴别诊断。
目的:确定散发性雅各布-克雅氏病(sCJD)患者在疾病过程中的误诊,并确定哪些医学专业在正确诊断之前看到了sCJD患者,以及在疾病过程中的什么时候做出了正确的诊断。设计:回顾性病历回顾。环境:三级学术医疗中心的专科转诊中心。参与者:163名连续患者,历时5.5年,最终病理证实为sCJD。该研究使用了97名患者的子集,我们有足够的医疗记录。主要结局指标:在鉴别诊断中考虑的其他诊断和评估sCJD患者的医学专业类型。结果:最终分析使用了97例受试者的病历。误诊最常见的疾病类别是神经退行性疾病、自身免疫/副肿瘤、感染性疾病和毒性/代谢疾病。最常见的个体误诊是病毒性脑炎、副肿瘤疾病、抑郁症、眩晕、阿尔茨海默病、中风、不明原因痴呆、中枢神经系统血管炎、周围神经病变和桥本脑病。最常误诊的医生是初级保健医生和神经科医生;在第一次评估时被正确诊断的18%的患者中,诊断几乎总是由神经科医生做出的。从发病到诊断的平均时间为7.9个月,平均为病程的三分之二。结论:sCJD的诊断相当滞后。在评估疑似神经退行性、自身免疫性、感染性或毒性/代谢性病因的快速进展性痴呆患者时,sCJD也应纳入鉴别诊断,并应考虑适当的诊断检查,如弥散性脑磁共振成像。初级保健医生和神经科医生在sCJD诊断方面需要改进培训。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of neurology
Archives of neurology 医学-临床神经学
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