Flanagan's condensed protocol for neurodegenerative diseases. Implementation in a clinical autopsy setting with partial supervision of a neuropathologist.

IF 3.4 3区 医学 Q1 PATHOLOGY
Virchows Archiv Pub Date : 2024-12-01 Epub Date: 2024-03-12 DOI:10.1007/s00428-024-03781-0
Aitana López, Samuel López-Muñoz, Gabriela Caballero, Natalia Castrejon, Leonardo Rojo, Nuria Vidal-Robau, Abel Muñoz, Estrella Ortiz, Maite Rodrigo, Adriana García, Miriam Cuatrecasas, Teresa Ribalta, Iban Aldecoa
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Abstract

The Condensed Protocol (CP) was originally developed for the evaluation of Alzheimer's Disease (AD) and other neurodegenerative diseases as a workable alternative to the complex and costly established autopsy guidelines. The study objective is to examine the degree of implementation of the CP in the pathology department of a third level university hospital in a period of 5 years. Clinical autopsies performed between 2016 and 2021 on patients aged 65 years or over and did not require a specific neuropathological examination were reviewed. Histological screening and staging of neurodegenerative diseases was performed using the original immunohistochemical stains. Out of 255 autopsies, 204 met the inclusion criteria and 190 could be reviewed. The CP was applied to 99 cases; histological signs of neurodegenerative disease were observed in 92. Sampling errors were detected in 59 cases. Immunohistochemical studies were performed in 68 cases. The diseases identified were: 31 cases of AD (12 low grade; 19 intermediate), 18 amyloid angiopathy, 15 primary age-related tauopathy, 6 argyrophilic grain disease, 3 progressive supranuclear palsy, 1 Lewy body disease (of 22 cases), and 2 limbic-predominant age TDP43 encephalopathy (of 5 cases). In 30 out of 83 cases, there was more severe vascular pathology in complete sections of frontal cortex and lentiform nucleus. The CP allows reliable detection and staging of AD and related neurodegenerative diseases in clinical autopsies. However, supervision by a neuropathologist seems necessary for a fully successful implementation of the CP in a clinical hospital setting.

Abstract Image

弗拉纳根神经退行性疾病浓缩方案。在神经病理学家的部分指导下,在临床尸检环境中实施。
浓缩方案(CP)最初是为评估阿尔茨海默病(AD)和其他神经退行性疾病而开发的,是复杂且昂贵的既定尸检指南的可行替代方案。本研究的目的是考察一家三级甲等大学医院病理科在 5 年时间里对 "特许方案 "的执行程度。研究回顾了 2016 年至 2021 年期间对 65 岁或以上且无需进行特定神经病理学检查的患者进行的临床尸检。使用原始免疫组化染色对神经退行性疾病进行了组织学筛查和分期。在 255 例尸体解剖中,204 例符合纳入标准,190 例可进行复查。对 99 例病例进行了 CP 分析;在 92 例病例中观察到了神经退行性疾病的组织学迹象。在 59 个病例中发现了取样错误。对 68 例病例进行了免疫组化研究。确定的疾病有31例AD(12例低度;19例中度)、18例淀粉样血管病、15例原发性年龄相关性tau病、6例霰粒细胞病、3例进行性核上性麻痹、1例路易体病(共22例)和2例边缘优势年龄TDP43脑病(共5例)。在 83 个病例中,有 30 个病例的额叶皮层和扁桃体核完整切片存在较严重的血管病变。在临床尸检中,CP 可以对 AD 和相关神经退行性疾病进行可靠的检测和分期。然而,要在临床医院环境中完全成功地实施 CP,神经病理学家的监督似乎是必要的。
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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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