Literature DB >> 22121349

Hippocampal microbleed on a post-mortem t(2)∗-weighted gradient-echo 7.0-tesla magnetic resonance imaging?

J De Reuck1, D Caparros-Lefebvre, V Deramecourt, C A Maurage.   

Abstract

The present post-mortem study of a brain from an Alzheimer patient showed on a T(2)∗-weighted gradient-echo 7.0-T MRI of a coronal brain section a hyposignal in the hippocampus, suggesting a microbleed. On the corresponding histological examination, only iron deposits around the granular cellular layer and in blood vessel walls of the hippocampus were observed without evidence of a bleeding. This case report illustrates that the detection of microbleeds on MRI has to be interpreted with caution.

Entities:  

Keywords:  Alzheimer dementia; Hippocampus; Iron deposits; Microbleed; Neuropathology; T2∗-weighted 7.0-T MRI sequence

Year:  2011        PMID: 22121349      PMCID: PMC3223029          DOI: 10.1159/000332611

Source DB:  PubMed          Journal:  Case Rep Neurol        ISSN: 1662-680X


Introduction

Cerebral microbleeds are frequently detected on magnetic resonance imaging (MRI) in patients with small-vessel diseases such as cerebral amyloid angiopathy and lipohyalinosis [1]. They are frequently observed in brains of patients suffering from Alzheimer dementia (AD) and are mainly related to cerebral amyloid angiopathy [2]. The clinical significance of microbleeds in AD is poorly understood [3]. Post-mortem verifications of MRI-detected microbleeds become more and more mandatory [4]. We present the clinical history and the post-mortem T2∗-weighted gradient-echo (GRE) 7.0-T MRI findings with the neuropathological correlates of a suspected hippocampal microbleed in a patient with AD.

Case Report

This female patient died at the age of 88 years from a neurodegenerative disease of unknown etiology. The prior clinical history included thrombophlebitis, complicated by lung embolism, gout, knee arthrosis, cholecystectomy and dyslipidemia. Memory disturbances started at the age of 82 years. She had a cognitive evaluation at the age of 86 years. On the Mattis Dementia scale she had a score of 102/144. An MRI of the brain showed bilateral hippocampal atrophy and symmetrical hypersignals in the brainstem on a T2 sequence. No T2∗ sequence was performed at that time. The patient's cognitive status rapidly deteriorated with periodic hallucinations. Rivastigmine dermal patches did not improve the mental status. The patient had frequent falls and became more and more dependent. She had many episodes of urinary retention. Walking became impossible due to the development of a parkinsonian syndrome with extreme axial rigidity. The patient had to enter a nursing home at the age of 87 years, due to rapid physical deterioration. She became bedridden, developed skin scars and died a few months later. Post-mortem brain examination was obtained by written informed consent from the nearest family. The brain tissue samples were first used for diagnosis and afterward integrated in the Lille Neuro-Bank, dependant from the Lille University and co-federated by the ‘Centre des Resources Biologiques’, acting as institutional review board. On histological examination the diagnosis of AD, stage VI, was made according to the Braak and Braak criteria [5]. Mild deposits of amyloid were found in a few cortical and leptomeningeal vessels. The bleeding load in the brain was quantified according to a method previously described [6]: only a few widespread small bleeds were observed. No other cerebrovascular lesions were found. Three coronal sections of a cerebral hemisphere were submitted to a T2∗-weighted GRE 7.0-T MRI, and afterwards compared to the corresponding histological sections for the detection of microbleeds, according to a previously described method [7]. A moderate number of hyposignals were observed, predominantly in the deep cortical layers of the central and occipital sections on the T2∗ sequence. All of them were confirmed to be small bleeds on the corresponding histological slides. In addition, a strong hyposignal was observed in the hippocampus (fig. ). However, the corresponding histological slide showed only amorphous iron deposits around the granular cellular layer and inside the layer of pyramidal neurons (fig. ). Moreover, iron deposits were present in the walls of small vessels (fig. ).

Discussion

The present study shows a false-positive microbleed signal in the hippocampus on a T2∗ weighted GRE 7.0-T MRI sequence, due to iron deposition. Overall, cerebral microbleeds are rarely observed in the hippocampus, compared to other brain regions, in patients with suspected cerebrovascular disease [8]. Brain iron deposits are mainly observed in the basal ganglia and were recently found to be associated with general cognitive ability and cognitive ageing [9]. Increased iron accumulation has been demonstrated in the hippocampus of AD brains [10, 11]. This case report shows that one has to be careful in the interpretation of hyposignals as microbleeds on T2∗ sequence MRI.
  11 in total

1.  Comparison of 7.0-T T₂*-magnetic resonance imaging of cerebral bleeds in post-mortem brain sections of Alzheimer patients with their neuropathological correlates.

Authors:  J De Reuck; F Auger; C Cordonnier; V Deramecourt; N Durieux; F Pasquier; R Bordet; C A Maurage; D Leys
Journal:  Cerebrovasc Dis       Date:  2011-03-21       Impact factor: 2.762

2.  High-field magnetic resonance imaging of brain iron in Alzheimer disease.

Authors:  John F Schenck; Earl A Zimmerman; Zhu Li; Sudeshna Adak; Angshuman Saha; Reeti Tandon; Kenneth M Fish; Clifford Belden; Robert W Gillen; Anne Barba; David L Henderson; William Neil; Timothy O'Keefe
Journal:  Top Magn Reson Imaging       Date:  2006-02

Review 3.  Evolution of neuronal changes in the course of Alzheimer's disease.

Authors:  H Braak; E Braak
Journal:  J Neural Transm Suppl       Date:  1998

4.  Post-mortem MR brain imaging comparison with macro- and histopathology: useful, important and underused.

Authors:  J M Wardlaw
Journal:  Cerebrovasc Dis       Date:  2011-03-21       Impact factor: 2.762

Review 5.  Brain microbleeds and Alzheimer's disease: innocent observation or key player?

Authors:  Charlotte Cordonnier; Wiesje M van der Flier
Journal:  Brain       Date:  2011-01-21       Impact factor: 13.501

6.  Brain iron deposits are associated with general cognitive ability and cognitive aging.

Authors:  Lars Penke; Maria C Valdés Hernandéz; Susana Muñoz Maniega; Alan J Gow; Catherine Murray; John M Starr; Mark E Bastin; Ian J Deary; Joanna M Wardlaw
Journal:  Neurobiol Aging       Date:  2010-06-09       Impact factor: 4.673

7.  Prevalence of small cerebral bleeds in patients with a neurodegenerative dementia: a neuropathological study.

Authors:  Jacques De Reuck; Vincent Deramecourt; Charlotte Cordonnier; Didier Leys; Florence Pasquier; Claude-Alain Maurage
Journal:  J Neurol Sci       Date:  2010-10-20       Impact factor: 3.181

8.  Cerebral microbleeds - prevalence, distribution and risk factors in northeast population without preceding large-area stroke.

Authors:  Peng-fei Liu; Ying-zhe Cui; Jing Na; Pei-yi Gao
Journal:  Chin Med J (Engl)       Date:  2010-02-05       Impact factor: 2.628

9.  The impact of cerebral amyloid angiopathy on the occurrence of cerebrovascular lesions in demented patients with Alzheimer features: a neuropathological study.

Authors:  J De Reuck; V Deramecourt; C Cordonnier; D Leys; C A Maurage; F Pasquier
Journal:  Eur J Neurol       Date:  2011-01-18       Impact factor: 6.089

Review 10.  Spontaneous brain microbleeds: systematic review, subgroup analyses and standards for study design and reporting.

Authors:  Charlotte Cordonnier; Rustam Al-Shahi Salman; Joanna Wardlaw
Journal:  Brain       Date:  2007-02-24       Impact factor: 13.501

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Authors:  Geetika Nehra; Bjoern Bauer; Anika M S Hartz
Journal:  Pharmacol Ther       Date:  2022-01-30       Impact factor: 13.400

Review 2.  Cerebral microbleeds: a review of clinical, genetic, and neuroimaging associations.

Authors:  Paul A Yates; Victor L Villemagne; Kathryn A Ellis; Patricia M Desmond; Colin L Masters; Christopher C Rowe
Journal:  Front Neurol       Date:  2014-01-06       Impact factor: 4.003

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