诊断额颞叶变性。
Making the diagnosis of frontotemporal lobar degeneration.
机构信息
Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
出版信息
Arch Pathol Lab Med. 2013 Mar;137(3):314-25. doi: 10.5858/arpa.2012-0075-RA.
CONTEXT
Autopsy evaluation of the brain of a patient with frontotemporal dementia (FTD) can be daunting to the general pathologist. At some point in their training, most pathologists learn about Pick disease, and can recognize Pick bodies, the morphologic hallmark of Pick disease. Pick disease is a type of frontotemporal lobar degeneration (FTLD), the general category of pathologic process underlying most cases of FTD. The 2 major categories of pathologic FTLD are tauopathies (FTLD-tau) and ubiquitinopathies (FTLD-U). Pick disease is one of the FTLD-tau subtypes and is termed FTLD-tau (PiD).
OBJECTIVE
To "demystify" FTLDs, and to demonstrate that subtypes of FTLD-tau and FTLD-U can be easily determined by following a logical, stepwise, histochemical, and immunohistochemical investigation of the FTD autopsy brain.
DATA SOURCES
Previously published peer-reviewed articles.
CONCLUSIONS
The hope is that this article will be a useful reference for the general pathologist faced with performing a brain autopsy on a decedent with frontotemporal dementia.
背景
对患有额颞叶痴呆(FTD)的患者的大脑进行尸检评估可能会令普通病理学家感到畏惧。在其培训过程中的某个阶段,大多数病理学家都会了解到皮克病,并能够识别出皮克体,这是皮克病的形态学标志。皮克病是额颞叶变性(FTLD)的一种类型,是大多数 FTD 病例背后的病理过程的一般类别。病理 FTLD 的 2 个主要类别是tau 病(FTLD-tau)和泛素病(FTLD-U)。皮克病是 FTLD-tau 亚型之一,称为 FTLD-tau(PiD)。
目的
“揭开”FTLD 的神秘面纱,并证明通过对 FTD 尸检大脑进行逻辑、逐步、组织化学和免疫组织化学研究,很容易确定 FTLD-tau 和 FTLD-U 的亚型。
数据来源
之前发表的同行评议文章。
结论
希望本文能为面对进行额颞叶痴呆尸检的普通病理学家提供有用的参考。