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Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man

  • Laure Saint-Aubert1,
  • Jérémie Pariente2, 3, 4,
  • Herve Dumas5,
  • Pierre Payoux2, 3, 6,
  • Jean-Philippe Brandel7,
  • Michèle Puel2, 3, 4,
  • Anne Vital8,
  • Eric Guedj9,
  • Suzanne Lesage10,
  • Katell Peoc’h11,
  • Christine Brefel Courbon2, 3, 4, 12 and
  • Fabienne Ory Magne2, 3, 4Email author
BMC NeurologyBMC series – open, inclusive and trusted201616:122

https://doi.org/10.1186/s12883-016-0643-y

Received: 19 November 2015

Accepted: 22 July 2016

Published: 30 July 2016

Abstract

Background

Few patients are reported with dementia with Lewy bodies before fifty years-old, which may partly reflect the difficulty of accurate diagnosis in young population. We report the case of a 44-year-old male with pathologically confirmed sporadic dementia with Lewy bodies, who did not fulfil the revised clinical criteria for this disease.

Case presentation

We document this atypical case with clinical and cognitive evaluation, imaging, biochemistry, genetics and pathology investigations. Creutzfeldt-Jakob disease was first suspected in this patient with no previous medical history, who developed acute and rapid cognitive impairment, L-dopa-non-responsive parkinsonism, and delusion. Positive 14–3–3 protein was initially detected in cerebrospinal fluid and until the late stages of the disease. Severe atrophy with no diffusion hypersignal was found on structural MRI as well as an extensive hypometabolism on 18F-FDG-PET, in comparison to age-matched healthy volunteers. Genetic investigation found no alpha-synuclein gene mutation. The patient died within 5 years, and post-mortem examination found numerous Lewy bodies and Lewy neurites consistent with pure Lewy body disease.

Conclusions

This comprehensively described case illustrates that dementia with Lewy bodies can occur in young patients with atypical clinical presentation. Biochemistry and neuroimaging investigations can sometimes be insufficient to allow accurate diagnostic. More specific markers to support such diagnosis are needed.

Keywords

Dementia with Lewy bodies 14–3–3 protein Diagnosis Genetics Imaging

Background

Dementia with Lewy bodies (DLB) is the second most common form of neurodegenerative dementia in the population over 65 years-old [1], with an age of onset varying from 50 to 80 [2]. The prevalence of DLB in younger patients remains unknown. The recent criteria for diagnosis of probable DLB require progressive cognitive decline, accompanied by two out of three core features: fluctuating alertness, recurrent visual hallucinations and spontaneous motor Parkinsonism [3]. Despite these criteria, clinical diagnosis of DLB may be difficult, and some cases may be misdiagnosed with other dementia such as Creutzfeldt-Jakob disease (CJD) [4]. Indeed, CJD cases may share clinical similarities with DLB such as dementia, visual disturbances and abnormal movements (parkinsonism, myoclonia, dystonia and chorea). Nevertheless, the onset of the symptoms in CJD is usually acute while insidious in DLB. We report the case of a 44 year-old patient with acute dementia, first mimicking CJD, but proved to have DLB at autopsy. Clinical, neuropsychological, imaging and biological investigations are reported.

Case presentation

Clinical follow-up

  • Month 0: A 44 year-old man, 12 years of education, started complaining acutely of slowness and sustained attention difficulties. He had neither clinical comorbidities nor relevant familial history.

Within three weeks after the first complaints, his status rapidly worsened and the patient needed help for every daily life activities. He was hospitalized, and presented significant cognitive impairment and walking difficulties related to marked parkinsonian syndrome. Depression with suicidal ideation was reported. No cerebellar features were observed. Neuropsychological assessment showed marked cognitive slowness and impairment of anterograde memory, mental calculation, verbal fluency, praxies and mental flexibility (Table 1). Electroencephalogram (EEG) showed slow cerebral activity without any epileptic or pseudo periodic abnormalities. Tianeptine and ropinirole treatments were introduced.
Table 1

Clinical, neuropsychological and biological assessments for the patient

 

M0

M2

M7

M15

M27

M43

Neuropsychological assessment

 

Global cognitive state

 MMSE

25

25

24

21

17

13

Speed processing

 TMT part A, time (seconds)

133

157

144

193

NA

NA

Short term memory

 WAIS III digit span forward

4

5

5

5

3

NA

 WAIS III digit span backward

3

3

2

3

2

NA

Executive functions

 Phonemic verbal fluency: letter ‘p’

12

1

6

10

NA

NA

 Semantic verbal fluency: ‘animal’ category

15

16

16

12

NA

NA

 FAB (/18)

12

12

12

10

6

2

 TMT part B, time (seconds)

296

537

486

NA

NA

NA

 TMT part B, mistakes

0

1 (help)

1

Anterograde verbal memory

FCSRT

 sum of free recalls (/48)

19

18

27

22

8

NA

 sum of free + cued recalls (/48)

42

47

46

45

NA

NA

 recognition (/48)

47

48

48

45

NA

NA

 delayed free recall (/16)

9

6

8

6

NA

NA

 delayed free + cued recall (/16)

14

14

16

15

NA

NA

Anterograde visual memory

 Rey complex figure, memory (/36)

< centile 10

-

-

-

NA

NA

Language

 DO80 (/80)

-

-

60

-

NA

NA

Visuoconstructive praxies

 Rey complex figure, copy (/36)

25

12

13.5

-

NA

NA

EEG

      
 

Slow cerebral activity

No epileptic or pseudo-periodic abnormalities

-

PSWC discharges during hyperpnea

unchanged

-

-

Cognitive domains are mentioned in bold characters. Abbreviations: M month, NA Not achievable by the patient, “-” not available, “help” the patient needed help to achieve the test, MMSE Mini Mental State Evaluation, TMT Trail Making Test, FCSRT Free and Cued Selective Recall Reminding Test, FAB Frontal Assessment Battery, EEG electroencephalogram, PSWC periodic sharp-wave complex

  • Month 2: His condition worsened, and he was hospitalized in the Department of Neurology, in University Hospital, Toulouse, France. In the absence of sustained stimulation, the patient remained motionless and speechless, due to severe apathy. Falls occurred frequently (about once a day), due to altered postural reflexes. After marked stimulation, it was noticed that the patient was depressed but not melancholic or suicidal. Marked symmetric and axial parkinsonian syndrome did not improve after L-dopa challenge. Slight reflex myoclonus was noticed in the upper limbs. Ocular saccades were slow but not limited. Apraxia and executive dysfunctions had worsened. Detection of 14–3–3 protein performed from cerebrospinal fluid (CSF) sample by western-blot was positive, whereas cytology and biochemistry were normal. Structural cerebral MRI revealed fronto-temporal atrophy on visual assessment of T1 sequence, with no abnormality on diffusion weighted imaging (DWI). Ropinirole, and tianeptine treatments were replaced by citalopram, oxazepam and zopliclone.

  • Month 6: Daily risperidone treatment was introduced due to delusions of persecution and rare visual hallucinations.

  • Month 7: Parkinsonism did not deteriorate with the addition of neuroleptic agents. Delusions and hallucinations remained present, although less prominent, and cognitive functions kept worsening. Structural MRI was unchanged, and 18F-FDG-PET visual assessment showed severe hypometabolism in parietal regions.

  • Month 10: The patient only experienced few hallucinations without delusions. Risperidone treatment was stopped but parkinsonian symptoms had worsened: he had severe dysarthria and was not able to walk without assistance because of his instability.

The patient had to be institutionalized 12 months after symptoms onset.
  • Month 20: Axial parkinsonian symptoms had worsened: he had difficulties swallowing, severe dysarthria, freezing in narrow place and total loss of postural reflexes. He was bed-ridden most of the day. CSF 14–3–3 protein remained positive, while total-tau (238 pg/mL) and Aβ42 (511 pg/ml) levels were within the normal ranges (norm < 450 pg/mL and > 500 pg/mL, respectively).

MRI showed moderate striatal, brainstem, and bilateral fronto-temporo-parietal atrophy on visual assessment.
  • Month 43: Parkinsonian symptoms were very severe, and myoclonus more pronounced. Important perseverations, imitations, and grasping were reported. Speech was unintelligible. Detection of 14–3–3 protein in CSF was negative.

The patient died one year later, aged 49, after a total duration of 55 months. Cerebral histopathological examination was performed.

Imaging analyses

Grey matter density was assessed in our patient from his first T1 MRI sequence (Fig. 1a), and compared to the grey matter density of a group of 30 age-matched healthy controls (age = 44.9 ± 3.8) from the online database OASIS (http://www.oasis-brains.org/), using a whole brain z-score map. The 18F-FDG-PET scan from our patient (Fig. 1c) was also compared to another group of 23 age-matched healthy controls (age = 44.3 ± 9.4) using z-scores map (for details on the control population and imaging processing procedures, see Additional file 1). All z-scores below −2 or above 2 were considered as significant.
Fig. 1

MRI and 18F-FDG-PET imaging. Patient’s MRI T1 sequence at M2 (a) and 18F-FDG–PETscan at M43 (c). Comparison between the patient and (b) age-matched healthy controls (n = 30) for grey matter density, (d) age-matched healthy controls (n = 23) for 18F-FDG uptake. Patient’s cortical atrophy below −2 standard deviations is displayed with a white to dark red scale. Patient’s hypometabolism below −2 standard deviations is displayed with a light green to dark blue scale while hypermetabolism is displayed with an orange to yellow scale. R = Right side

The patient showed global bilateral decrease of grey matter density affecting all cortical regions as well as subcortical structures and cerebellum (Fig. 1b and Additional file 2). Negative z-scores below −5 were found in parietal, temporal, but also frontal and insular cortices. Left hippocampus and bilateral thalami were spared. No z-score > 2 was found.

Regarding 18F-FDG-PET, the patient showed widespread significant bilateral hypometabolism, encompassing all cerebral lobes, most predominant in the parietal lobe (Fig. 1d and Additional file 2). Negative z-scores below −8 were found in parietal and medial temporal regions. No difference compared to controls was found in the thalamus, orbitofrontal regions, or the posterior cingulate. Hypermetabolism was found in the putamen.

Histopathology

Preliminary examination was carried out on hematoxylin-eosin stained paraffin sections, completed by immunohistochemistry with the following antibodies: anti-tau AT8 (Thermo Fisher Scientific, Illkirch, France), anti-amyloid-beta A4 (Dako, Trappes, France), anti-alpha-synuclein (Leica Biosystems, Newcastle, UK), and anti-prion protein 12 F10 (Spibio, Montigny Le Bretonneux, France). Macroscopic brain examination showed a marked palor of the substantia nigra, while anti-alpha-synuclein immunohistochemistry revealed numerous Lewy bodies and Lewy neurites in the frontal and temporal cortices, hippocampus, substantia nigra, locus cœruleus, as well as in the dorsal motor nucleus of the vagus, occipital and entorhinal cortices, and more rarely in the thalamus, caudate nucleus, putamen, and pallidum (Fig. 2). Spongiosis was absent and anti-prion protein immunohistochemistry was negative. A few AT8-positive neurofibrillary tangles were noticed in the hippocampus and the entorhinal cortex, whereas anti-amyloid-beta 4 staining revealed neither neocortical deposits nor amyloid angiopathy.
Fig. 2

Post-mortem tissue staining. a and c Hematoxylin and eosin stained section of the frontal cortex (a) and the substantia nigra (b). Black arrows point at Lewy bodies in pigmented neurons. Bar scale = 20 μm. b, d and e Immuno-histochemistry with anti-alpha synuclein showing Lewy bodies in the frontal cortex (c), the substantia nigra (d) and the locus cœruleus (e)

Molecular genetics

SNCA gene (encoding the alpha-synuclein) mutations were investigated using bidirectional Sanger sequencing on an ABI 3730 automated sequencer (Applied Biosystem) and SeqScape v2.6 software (Applied Biosystems), and multiplex ligation-dependent probe amplification (MLPA, MRC-Holland). PRNP gene (encoding the prion protein) mutations were investigated using a previously described protocol [5]. Neither missense mutations nor multiplications were found in the SNCA gene (alpha-synuclein), and no mutation was identified in the PRNP gene (prion protein) either. The polymorphism at codon 129 was methionine-methionine.

Conclusions

We report the case of a young patient with confirmed DLB that did not fulfil the revised clinical criteria [3] (see Table 2). Global cognitive impairment was indeed acute at onset, while progressive impairment is a mandatory requirement for DLB diagnosis. Moreover, no fluctuating cognition was observed during follow-up, while 75 % of DLB patients experience such fluctuations, which are a core feature of typical DLB [6]. Our patient also experienced slight visual hallucinations for one year, in a context of severe paranoid delusion without neuroleptic sensitivity, while delirium duration is usually short in DLB [7]. Moreover, hallucinations may also occur in CJD [8].
Table 2

Early diagnostic profile of the case according to the revised criteria for the clinical diagnosis of dementia with Lewy bodies (DLB) – adapted from McKeith et al., Neurology 2005 [3]

 

Dementia with Lewy bodies

Creutzfeldt-Jakob disease

Case reported

Central feature

 Cognitive decline

Progressive, insidious onset

Acute or rapidly progressive

Acute

 Prominent or persistent memory impairment

Not early: usually evident with progression

Early

Early

 Prominent deficits of attention, executive function, and visuospatial ability

Yes

No (global dementia)

No (global cognitive impairment)

Core features

 Fluctuating cognition

Yes

No

No

 Recurrent visual hallucination

Yes

Yes

No (mainly delirious with few hallucinations)

 Spontaneous features of parkinsonism

Yes

Yes

Yes

Suggestive features

 REM sleep behavior disorder

Yes

No

Not reported by the wife

 Severe neuroleptic sensitivity

Yes

No

No

 Low dopamine uptake in basal ganglia on imaging

Yes

Very rare (one case reported [22])

Not performed (the case was parkinsonian)

Supportive features (Commonly present in DLB but not proven to have diagnostic specificity)

 Repeated falls and syncope

Yes

No

Yes

 Transient loss of consciousness

Yes

No

No

 Severe autonomic dysfunction

Yes

No

No

 Hallucinations in other modalities

Yes

No

No

 Systematized delusions

Yes

No

Yes

 Depression

Yes

Yes

Yes

 Relative preservation of medial temporal lobe structures on MRI

Yes

Yes

Yes

 Generalized low uptake on PET perfusion scan with reduced occipital activity

Yes

No

Extensive hypometabolism

 Prominent slow wave activity on EEG with temporal lobe transient sharp waves

Yes

No (biphasic and triphasic periodic complex)

Slow but without temporal lobe transient sharp waves

Other

 Mean age of onset (years)

75

70

42

 Mean duration (years)

7

0.5

5

 Detection of 14.3.3 protein

Rarely (3 cases reported)

Yes

Yes

Probable DLB Two core features or one core feature and one or more suggestive features, Possible DLB Up to one core feature and one or more suggestive features

Features for Creutzfeldt-Jakob disease are adapted from the MRI-CJD Consortium criteria for sporadic Creutzfeldt–Jakob disease [8]

The patient’s clinical presentation was similar to the cognitive subtype of CJD described by Puoti et al. [9], with acute dementia, confusion and cortical visual disturbance, extrapyramidal signs and myoclonus. Although MRI did not show diffusion abnormalities, such clinical presentation and positive 14.3.3 protein detection were consistent with CJD diagnosis [8]. Cases of DLB are reported in neuropathological series of suspected CJD [4, 1012]. But in these series, patients are at least 60 years-old; symptomatic progression is rapid and leads to death within one to two years. Despite an acute onset, our 44-year-old patient showed a clinical progression and disease duration similar to usual DLB [13], and no longer fulfilled the clinical criteria for sporadic CJD disease [8] two years later.

Interestingly, patients suspected for CJD during lifetime but with confirmed DLB at autopsy often share myoclonus, pyramidal and extrapyramidal symptoms [10]. While fluctuating cognition and repeated falls are rare, hallucinations and akinetic mutism are variable among the series. When performed, 14–3–3 protein detection is negative in most cases, except for Van Everbroeck and colleagues who reported rare 14–3–3 protein positivity (less than 20 % of definite DLB) [14]. Of note, a recent study presented tau protein levels as a better marker than 14–3–3 protein in the diagnosis of CJD [15]. After 2 years of clinical evolution, CSF total tau level was within the normal range, confirming the hypothesis that our patient had no CJD.

As observed in our case, none of the previously reported confirmed LBD patients with suspicion of CJD had cerebellar symptoms, or hypersignal on MRI, but most of them had diffuse cortical atrophy [10]. Regarding our patient, comparison to a control population revealed a wide bilateral atrophy involving all cortical regions, as well as subcortical nuclei such as the putamen and the pallidum. Decrease of grey matter density in the insula and the putamen has been recently reported as a characteristic pattern of atrophy in patients with DLB [16]. This pattern should also include lateral temporal atrophy, but we reported a broader pattern of atrophy, including other cortical regions. This extended atrophy suggests an advanced stage of the pathology in the patient’s brain, although the MRI used was performed soon after clinical onset.

The patient also presented with widespread cortical hypometabolism, sparing orbitofrontal regions as well as posterior cingulate and thalamus. Interestingly, we found bilateral hypermetabolism in the posterior part of the putamen. To our knowledge, this is the first report of striatal hypermetabolism in DLB [17]. Compensatory mechanisms may explain this finding, but further investigations are required.

While mean age of onset for DLB is usually 75 years old, ranging from 50 to 80, DLB can also be an uncommon cause of dementia in young patients [18]. Few patients have been reported with DLB before 50 years-old [2]. Most of them were reported in Japan [19], although they did not fulfill the revised criteria for DLB, and may not have had pure DLB [20]. Because our case was sporadic and because parkinsonism was the core clinical feature, molecular genetic analysis was limited to the alpha synuclein and prion protein genes. However, other genetic variations were also reported in DLB [21]. In this case, the implication of these other genes is unlikely, considering the pathological findings of Lewy bodies and Lewy neurites without beta amyloid plaques or widespread neurofibrillary tangles.

In summary, our case illustrates that DLB can occur in young patients with an atypical and severe clinical presentation, which can first be mistaken for CJD. Laboratory and neuroimaging investigations are useful to exclude systemic and pharmacological causes of delirium and cognitive impairment, but remain insufficient to allow an accurate diagnostic of DLB, particularly in young patients. Specific markers to support such diagnosis are needed.

Abbreviations

CJD, Creutzfeldt-Jakob Disease; CSF, Cerebrospinal Fluid; DLB, Dementia with Lewy Bodies; FDG, Fluorodeoxyglucose; MRI, Magnetic Resonance Imaging; PET, Positron Emission Tomography

Declarations

Acknowledgments

The authors would like to thank the healthy control individuals for their participation, and are grateful to Antoine Leuzy for his valuable help on language correction.

Funding

This work was supported by NIH grants: number P50 AG05681, P01 AG03991, R01 AG021910, P20 MH071616, U24 RR021382, as funding sources of the OASIS database that provided the healthy controls MRI data.

Availability of data and materials

The datasets supporting the conclusions of this article are publically available.

Authors’ contributions

LSA analyzed the imaging data and drafted the manuscript; JP acquired clinical data from the case and critically revised the manuscript; HD provided and interpreted MRI data from the case and critically revised the manuscript; PP provided and interpreted PET data from the case and critically revised the manuscript; JPB acquired clinical data from the case and critically revised the manuscript; MP acquired clinical data from the case and critically revised the manuscript; AV performed the histopathology analyses and critically revised the manuscript; EG provided and interpreted PET data from the healthy control group and critically revised the manuscript; SL performed the biomolecular analyses for genetics and critically revised the manuscript; KP performed the biomolecular analyses for genetics and critically revised the manuscript; CBC acquired clinical data from the case and critically revised the manuscript; FOM designed the study, acquired clinical data from the case and drafted the manuscript.

All co-authors approved the final version of the manuscript. FOM had full access to all the data in the study, is the guarantor of the study and takes responsibility for the integrity of the study, the data and the accuracy of the data analysis.

Authors’ information

LSA is a postdoctoral fellow at Karolinska Institutet with a background in Neuroscience; JP is a neurologist, MD, PhD, working at Purpan Toulouse Hospital (France) in the Department of Neurology, Memory Unit; specialized in dementia; HD is a neuroradiologist, MD, working at Purpan Toulouse Hospital (France) in the Department of Radiology; PP is a nuclear physicist, MD, PhD, working at Purpan Toulouse Hospital (France) in the Department of Nuclear Medicine and PET center; JPB is a neurologist, MD, coordinator of the National Reference Department of CJD at the Salpêtrière Hospital (France); specialized in dementia and movement disorders; MP is a neurologist, MD, who worked at Purpan Toulouse Hospital (France) in the Department of Neurology, Memory Unit; specialized in dementia; AV is a neuropathologist, MD, PhD, Professor at the Department of Pathology-Neuropathology in Bordeaux University Hospital (France); EG is a nuclear physicist, MD, PhD, working at Marseille Hospital (France) in the Department of Nuclear Medicine and PET center; SL is a molecular biologist, PhD, specialized in pathological genetics analyses; KP is a clinical biologist, PharmaD, PhD, associate professor at Paris Diderot University (France); CBC is a neurologist specialized in Parkinson’s disease and atypical Parkinsonism, MD, working at Purpan Toulouse Hospital (France) in the Department of Neurology, Abnormal Movements Unit; FOM is a neurologist specialized in Parkinson’s disease and atypical Parkinsonism, MD, working at Purpan Toulouse Hospital (France) in the Department of Neurology, Abnormal Movements Unit.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Written informed consent was obtained from the next of kin of the deceased patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Ethics approval and consent to participate

Procedures involving experiments on human subjects are done in accordance with the ethical standards of the Committee on Human Experimentation of the institution in which the experiments were done and in accord with the Declaration of Helsinki of 1975.

All healthy participants included in this study gave written informed consent. The 18F-FDG PET data from healthy participants come from a clinical trial approved by local ethics committee under the registration number: NCT00484523.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department NVS, Center for Alzheimer Research, Translational Alzheimer Neurobiology, Karolinska Institutet
(2)
INSERM UMR825, Imagerie cérébrale et handicaps neurologiques
(3)
University of Toulouse, Imagerie cérébrale et handicaps neurologiques
(4)
Department of Neurology, University Hospital of Toulouse
(5)
Department of Neuroradiology, University Hospital of Toulouse
(6)
Department of Nuclear Medicine, University Hospital of Toulouse
(7)
AP-HP, Cellule Nationale de Référence des Maladies de Creutzfeldt-Jakob, Groupe Hospitalier Pitié-Salpêtrière; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ. Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière, ICM
(8)
Department of Pathology, University Hospital of Bordeaux
(9)
Aix-Marseille University, CNRS, UMR7289, INT
(10)
Sorbonne Universities, UPMC (Paris 6), Inserm U1127, CNRS UMR 7225, and ICM
(11)
Department of Biochemistry, APHP, Lariboisière Hospital
(12)
Department of Clinical Pharmacology, University of Medicine

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Copyright

© The Author(s). 2016

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