[Frontotemporal dementia].

Raguna Nagy, J. Heuckmann, H. Mennel, J. Klosterkötter, J. Kuhn
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引用次数: 5

Abstract

BACKGROUND Among the primary degenerative dementias, frontotemporal dementia (FTD, Pick's disease) is very important along with Alzheimer's disease. The estimated prevalence is 15:100,000 in the 45- to 64-year-old population; thus, it appears that the FTD as a cause for so-called presenile dementia is nearly as common as Alzheimer's disease. CASE REPORT The case of a 52-year-old woman is described that presented with slowly progressive lack of concentration and disturbance of memory. Furthermore, the immediate family had noticed a change in her premorbid personality. Due to additional depressive symptoms, she was misdiagnosed with depressive pseudodementia first. CONCLUSION Since the clinical presentation of FTD is variable and the correct classification has been uncertain for a long time, clinical diagnosis can be very difficult, so that the disease is often detected too late or remains completely misdiagnosed. On this basis, pathology, clinical aspects, diagnosis, and therapeutic options of FTD will be demonstrated according to current standards of knowledge.
额颞叶痴呆。
背景:在原发性退行性痴呆中,额颞叶痴呆(FTD, Pick’s disease)与阿尔茨海默病(Alzheimer’s disease)并列。在45至64岁人群中,估计患病率为15:10万;因此,似乎FTD作为所谓的老年痴呆症的原因几乎和阿尔茨海默病一样常见。病例报告:病例描述一名52岁女性,表现为缓慢进行性注意力不集中和记忆障碍。此外,她的直系亲属注意到她病前的性格发生了变化。由于附加的抑郁症状,她首先被误诊为抑郁症假性痴呆。结论由于FTD临床表现多变,且长期不确定正确的分型,临床诊断非常困难,常常发现过晚或完全误诊。在此基础上,将根据目前的知识标准,展示FTD的病理、临床方面、诊断和治疗方案。
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
Medizinische Klinik
Medizinische Klinik 医学-医学:内科
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