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Knowing and not knowing: practical reflections on video based feedback as part of neuro-rehabilitation in a case of persistent anosognosia for hemiplegia. 知道和不知道:视频反馈作为偏瘫患者持续性病感失认的神经康复的一部分的实际反思。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-10 DOI: 10.1080/13554794.2024.2439568
Jenny Allum, Max Whittaker, Huw Green

We report the case of DT, a man in his fifties who suffered a large right fronto-parietal hemorrhage, resulting in a dense left weakness and a persistent anosognosia for the resultant hemiplegia. DT engaged in several video-feedback sessions. Video feedback therapy has been successful in previously reported cases of anosognosia, resulting in immediate and lasting resolution. In the current case, similarly dramatic effects were observed, but with a subsequent recurrence of the anosognosic ideation. The present case sheds light on the interplay of neurologic and psychological mechanisms involved in anosognosia and on some of the pragmatic emotional considerations of engaging in this form of rehabilitative therapy.

我们报告的情况下,DT,一个男人在他的五十谁遭受了一个大的右额顶叶出血,导致密集的左无力和持续的病感失认产生偏瘫。DT参与了几次视频反馈会议。视频反馈疗法在先前报道的病感失认病例中取得了成功,导致立即和持久的解决。在目前的病例中,观察到类似的戏剧性效果,但随后又出现了病感观念的复发。本病例揭示了病感失认症中涉及的神经学和心理学机制的相互作用,以及参与这种形式的康复治疗的一些实用情感考虑。
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引用次数: 0
Comprehensive evaluation and diagnosis of persistent vegetative state after hypoxic-ischemic encephalopathy: a case report. 缺氧缺血性脑病后持续植物人状态的综合评价与诊断1例。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-11-30 DOI: 10.1080/13554794.2024.2436682
Guohui Yang, Li Wang, Hongyu Xie, Xinwei Tang, Maisedi Mukedaisihan, Youbei Yang, Chenyu Fan, Junfa Wu, Yi Wu

We report a case of a 39-year-old woman with persistent vegetative state (PVS) following cardiac arrest and a right lower extremity fracture. Despite comprehensive rehabilitation for over 4 months, there was no improvement. Neuroelectrophysiological and neuroimaging assessments showed poor brain function, and the coma recovery scale-revised scale results suggested low arousal probability. Furthermore, patients with PVS exhibit autonomic reactivity and physiological responses to external stimuli. It is important to note that while these reactions may manifest as responsiveness to external stimuli, they should be interpreted as automatic physiological responses rather than indicative of consciousness.

我们报告一例39岁的女性持续植物人状态(PVS)后心脏骤停和右下肢骨折。尽管进行了4个多月的全面康复,但没有任何改善。神经电生理和神经影像学评估显示脑功能差,昏迷恢复量表-修正量表结果提示唤醒概率低。此外,PVS患者对外部刺激表现出自主反应性和生理反应。值得注意的是,虽然这些反应可能表现为对外部刺激的反应,但它们应该被解释为自动的生理反应,而不是意识的指示。
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引用次数: 0
A new GRN variant in logopenic variant primary progressive aphasia: a case report and literature review. 原发性进行性失语症中一种新的GRN变异:1例报告及文献复习。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-04 DOI: 10.1080/13554794.2024.2436215
Sha-Sha Jia, Pu-Lei Li, Ping Gao, Ye Jiang, Cheng-Liang Zhang, Wen-Wei Yun

The majority of genetic Primary progressive aphasia (PPA) patients harbor mutations in the granulin (GRN) gene. The present case showed impaired performances in single-word retrieval in spontaneous speech and naming, and repetition. Head MRI revealed marked lateral atrophy in the left parietal cortex. A diagnosis of logopenic variant PPA (lvPPA) was established. Genetic analysis showed a heterozygous 10-bp frameshift deletion in exon 4 of the GRN gene (NM_002087.4), leading to transformation of cysteine into alanine at amino acid 92 and creation of a premature stop codon at position 161. This patient represented a rare case of GRN-associated lvPPA. A new mutation site was detected in exon 4 of GRN gene.

大多数遗传性原发性进行性失语(PPA)患者携带颗粒蛋白(GRN)基因突变。本例患儿在自发言语、命名和重复中单字检索能力受损。头部MRI显示左侧顶叶皮层侧部明显萎缩。建立了血小板减少变异型PPA (lvPPA)的诊断。遗传分析显示,GRN基因(NM_002087.4)外显子4发生10 bp的杂合移码缺失,导致半胱氨酸在第92个氨基酸处转化为丙氨酸,并在第161个位置产生过早终止密码子。该患者为罕见的grn相关lvPPA病例。在GRN基因外显子4上检测到一个新的突变位点。
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引用次数: 0
Linguistic characteristics of primary progressive aphasia in a verb-final language. 动末语中原发性进行性失语症的语言特征。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-05 DOI: 10.1080/13554794.2024.2437152
Jee Eun Sung, Eun-Joo Kim, Sujin Choi, Jee Hyang Jeong

Purpose: The current study aimed to examine the linguistic characteristics of Korean-speaking individuals diagnosed with primary progressive aphasia(PPA).

Methods: Two individuals with agrammatic/non-fluent variants of nfvPPA and two with semantic variants of svPPA participated in this study. Picture description tasks were used to collect connected speech samples. Analysis focused on linguistic variables, including quantitative(number of utterances, words, nouns, and verbs), syntactic(mean length of utterance in morphemes, case markers per utterance, predicates per utterance), and semantic variables(correct information units, verb types). Additionally, participants completed two types of confrontation naming tasks.

Results: The nfvPPA group exhibited fewer linguistic units overall compared to the svPPA group, with noun-verb dissociation apparent only in the nfvPPA group. The svPPA group showed poorer performance in content-related linguistic variables. A notable clinical symptom specific to Korean, case marker deficits, was observed in the nfvPPA group.

Discussion: The study identified distinct linguistic patterns associated with the subtype of PPA in Korean speakers. The evaluation and interpretation of Korean-specific linguistic variables are crucial for classifying Korean-speaking individuals with PPA. Understanding these variables can enhance our comprehension of the unique linguistic deficits present in Korean PPA, particularly in relation to confrontation naming tasks and their implications for diagnosis and classification.

目的:本研究旨在探讨原发性进行性失语症(PPA)患者的语言特征。方法:两名具有nfvPPA语法/非流利变体的个体和两名具有svPPA语义变体的个体参与了本研究。使用图片描述任务来收集连接的语音样本。分析的重点是语言变量,包括数量变量(话语数量、单词、名词和动词)、句法变量(语素中话语的平均长度、每个话语的大小写标记、每个话语的谓语)和语义变量(正确的信息单位、动词类型)。此外,参与者完成了两种类型的对抗命名任务。结果:与svPPA组相比,nfvPPA组整体上表现出更少的语言单位,只有nfvPPA组出现了明显的名动分离。svPPA组在与内容相关的语言变量上表现较差。在nfvPPA组中观察到韩国人特有的显著临床症状,病例标记缺失。讨论:该研究确定了韩国语使用者中与PPA亚型相关的独特语言模式。韩国语特定语言变量的评估和解释对于韩国语个体的PPA分类至关重要。了解这些变量可以增强我们对韩国语PPA中存在的独特语言缺陷的理解,特别是在对抗命名任务及其对诊断和分类的影响方面。
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引用次数: 0
Sustained improvement of obsessive-compulsive symptoms following interruption of deep brain stimulation. 中断脑深部刺激后强迫症症状持续改善。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-16 DOI: 10.1080/13554794.2024.2441942
Israel Aristides de Carvalho Filho, Marcelo Queiroz Hoexter, Fabio L F Godinho, Ricardo F Iglesio, Igor Studart, Isabelle C Alencar, Katia G Benigno, Antonio Carlos Lopes

A 59-year-old male with severe treatment-resistant OCD achieved sustained symptom improvement after discontinuing deep brain stimulation (DBS) for over four years. Despite partial relief with ventral capsule/ventral striatum (VC/VS) DBS, complications led to device removal in 2018. Remarkably, the patient remained largely symptom-free, suggesting neuroplasticity changes in dysfunctional neurocircuits. This rare case highlights DBS's role in psychiatry, emphasizing the need for tailored surgical strategies and long-term follow-ups to optimize outcomes and understand DBS mechanisms.

一名患有严重治疗难治性强迫症的59岁男性患者在停止深部脑刺激(DBS)治疗四年多后,症状得到持续改善。尽管腹侧囊/腹侧纹状体(VC/VS) DBS部分缓解,但并发症导致2018年器械移除。值得注意的是,患者基本上没有症状,这表明功能失调的神经回路发生了神经可塑性变化。这个罕见的病例突出了DBS在精神病学中的作用,强调了定制手术策略和长期随访的必要性,以优化结果并了解DBS机制。
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引用次数: 0
Behavioral variant frontotemporal dementia with pathogenic variant in MAPT presenting as dementia with Lewy body disease. 伴有MAPT致病变异的行为变异性额颞叶痴呆表现为路易体病痴呆。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-10 DOI: 10.1080/13554794.2024.2440548
Tianxu Xia, Clara Li, Ayuko Iverson, Jessica Spat-Lemus, Amy Woroch, Georges Naasan

A 75-year-old Chinese American man presented to behavioral neurology clinic for a second opinion of dementia with Lewy body disease (DLB). The clinical manifestations met the criteria for a probable DLB diagnosis. Yet, in-depth evaluation unveiled clinical history, family history, and neuroimaging evidences that suggested a diagnosis of behavioral variant frontotemporal dementia (FTD). A heterozygous pathogenic variant in the microtubule-associated protein Tau (MAPT) was identified through genetic testing and confirmed the diagnosis of autosomal dominant MAPT-related FTD. This case is the first reported instance of MAPT-related FTD presenting with well-formed visual hallucinations in an elderly Chinese American.

一名75岁美籍华人男子到行为神经病学诊所就诊,诊断为痴呆合并路易体病(DLB)。临床表现符合可能的DLB诊断标准。然而,深入的评估揭示了临床病史、家族史和神经影像学证据,提示诊断为行为变异性额颞叶痴呆(FTD)。通过基因检测发现微管相关蛋白Tau (MAPT)的杂合致病变异,并确认常染色体显性MAPT相关FTD的诊断。本病例是第一例报道的与mapt相关的FTD,在一位老年华裔美国人中表现为形成良好的视幻觉。
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引用次数: 0
Cotard's: a controlled single case study of putative perceptual, cognitive and psychological risk factors. 科塔氏症:对假定的知觉、认知和心理风险因素的对照单例研究。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-24 DOI: 10.1080/13554794.2024.2436207
Nicola M J Edelstyn, Elisa Di Rosa, Swathi Prabhu, Femi Oyebode

This case study explores the psychological and neuropsychological traits of a 55-year-old woman, D.R., who has Cotard's, believing her torso has dissolved and food bypasses her legs. Her delusion emerged amid major depressive disorder with psychotic features, following prodromal symptoms like body distortion and somatosensory abnormalities. A neuropsychological assessment during remission revealed low-level visual perceptual deficits in an otherwise intact cognitive profile. Subtle distortions in bodily signals and specific attribution styles were identified as vulnerability factors, suggesting that the delusion may emerge when already strained information processing systems are further challenged. This relates to models of delusion formation.

本案例研究探讨了一名患有科塔尔氏症的55岁女性的心理和神经心理学特征,她认为自己的躯干已经溶解,食物绕过了她的腿。她的妄想出现在具有精神病特征的重度抑郁症中,伴随着身体扭曲和躯体感觉异常等前驱症状。在缓解期间的神经心理学评估显示低水平的视觉知觉缺陷在其他完整的认知概况。身体信号的细微扭曲和特定的归因风格被认为是脆弱因素,这表明当已经紧张的信息处理系统受到进一步挑战时,这种错觉可能会出现。这与错觉形成的模型有关。
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引用次数: 0
Schizophrenia misdiagnosis after dysmorphophobia in a patient with macrocephaly. 巨头症患者畸形恐惧症后精神分裂症误诊1例。
IF 0.6 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2025-02-01 Epub Date: 2024-12-12 DOI: 10.1080/13554794.2024.2439022
João Gama Marques, Josef Finsterer
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引用次数: 0
Visuoperceptual rehabilitation with repetitive transcranial magnetic stimulation in chronic cortical blindness: a case report. 反复经颅磁刺激治疗慢性皮质性盲的视觉康复一例报告。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-12-01 Epub Date: 2024-12-05 DOI: 10.1080/13554794.2024.2437195
Ozden Erkan Ogul, Suat Yılmaz, Ozge Arıca Duz, Fevzi Senturk, Lutfu Hanoglu

This study aims to reveal the effect of visuoperceptual rehabilitation combined with neuromodulation on visual impairment recovery in chronic cortical blindness. A 71-year-old patient with cortical blindness was assessed using perimetry, pattern electroretinogram (pERG), Canadian Occupational Performance Measurement (COPM), and Montreal Cognitive Assessment (MoCA) at baseline and after treatment. After 12 rTMS sessions and 50 visual perceptual rehabilitation sessions, perimetry, pERG, COPM, and MoCA significantly improved the visual field and daily functioning. Both COPM-MoCA scores exceeded clinical significance. The results indicate that combining vision therapy with rTMS may improve vision field, daily function, and satisfaction in a chronic blindness case.

本研究旨在探讨视知觉康复联合神经调节对慢性皮质性盲视力损害恢复的影响。我们对一位71岁的皮质性失明患者在治疗前和治疗后的视力、视网膜电图(pERG)、加拿大职业表现测量(COPM)和蒙特利尔认知评估(MoCA)进行了评估。经过12次rTMS治疗和50次视觉知觉康复治疗后,视野测量、pERG、COPM和MoCA显著改善了视野和日常功能。COPM-MoCA评分均超过临床意义。结果表明,视力治疗联合rTMS可改善慢性失明患者的视野、日常功能和满意度。
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引用次数: 0
A professional musician with progressive visuospatial concerns: a case study and review of musical alexia. 具有进步性视觉空间关注的专业音乐家:音乐失读症的个案研究与回顾。
IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-12-01 Epub Date: 2024-12-10 DOI: 10.1080/13554794.2024.2438413
Bronte Ficek-Tani, Samantha Tun, Alexander Frolov, Emily Sharp, Carolyn A Fredericks

This case report presents the story of Mr. S, a professional orchestral musician with declining musical sight-reading ability, followed by progressive visuospatial and language deficits. Our novel musical assessment battery revealed deficits in music-reading (musical alexia) and music-writing (musical agraphia), with spared auditory perception and expression. Taken with neuropsychological testing, clinical history, and imaging, we conclude that his symptoms evolved from musical alexia to a multidomain, neurodegenerative process centered in the dominant inferior parietal lobe and temporoparietal junction. We suspect a primary TDP-opathy with comorbid preclinical Alzheimer's disease. Mr. S's case highlights musical symptoms as meaningful, early indicators of neurodegeneration.

本病例报告介绍了专业管弦乐演奏家S先生的故事,他的音乐视读能力不断下降,随后出现了视觉空间和语言障碍。我们的新音乐评估电池揭示了音乐阅读(音乐失读症)和音乐写作(音乐失写症)的缺陷,而听觉感知和表达则幸免。通过神经心理学测试、临床病史和影像学检查,我们得出结论,他的症状从音乐失读症演变为以占优势的下顶叶和颞顶叶交界处为中心的多域神经退行性过程。我们怀疑原发性tdp病变合并临床前阿尔茨海默病。S先生的病例突出表明,音乐症状是神经退化的有意义的早期指标。
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引用次数: 0
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Neurocase
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