Literature DB >> 19095975

Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.

Charalampos Tzoulis1, Laurence A Bindoff.   

Abstract

BACKGROUND AND
PURPOSE: Most diffusion MRI studies of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode stroke-like lesions report high- or normal-apparent diffusion coefficient, and this has been used to differentiate stroke-like lesion from ischemic stroke. There are, however, 3 recent reports of restricted diffusion in the acute phase of the stroke-like lesions. The purpose of our study was to investigate this apparent paradox.
METHODS: We performed 9 serial MRI covering 2 stroke-like episodes in a 36-year-old man with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode caused by the common mitochondrial DNA mutation 3243A>G.
RESULTS: We found clear evidence of initial restricted diffusion in the stroke-like lesions, which gradually evolved to high-apparent diffusion coefficient as lesions aged. Evolution was, however, asynchronous with both high- and low-apparent diffusion coefficients temporally coexisting.
CONCLUSIONS: Our findings suggest that cytotoxic edema does occur early in the course of a stroke-like lesions and that its presence or, conversely, the absence of vasogenic edema, should not weaken the possibility of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode in favor of ischemic stroke.

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Year:  2008        PMID: 19095975     DOI: 10.1161/STROKEAHA.108.523118

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  16 in total

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Review 2.  Imaging of MELAS.

Authors:  Konark Malhotra; David S Liebeskind
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3.  Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients.

Authors:  Ji Hye Kim; Myung Kwan Lim; Tae Yeon Jeon; Joung Ho Rha; Jung Ho Rha; Hong Eo; So-Young Yoo; Chang Hae Shu
Journal:  Korean J Radiol       Date:  2011-01-03       Impact factor: 3.500

4.  Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation.

Authors:  Henriette J Tschampa; Horst Urbach; Susanne Greschus; Wolfram S Kunz; Cornelia Kornblum
Journal:  J Neurol       Date:  2012-11-30       Impact factor: 4.849

5.  Stroke and Stroke-like Episodes in Muscle Disease.

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Journal:  Open Neurol J       Date:  2012-05-18

6.  Paediatric Stroke: Review of the Literature and Possible Treatment Options, including Endovascular Approach.

Authors:  Elisa F Ciceri; Valeria Cuccarini; Luisa Chiapparini; Veronica Saletti; Luca Valvassori
Journal:  Stroke Res Treat       Date:  2011-07-07

7.  Mitochondrial encephalopathy, lactic acidosis, and stroke-like episode syndrome presenting with prolonged visual aura.

Authors:  Ileok Jung; So-Hee Park; Dong Wook Kim
Journal:  J Clin Neurol       Date:  2015-01-02       Impact factor: 3.077

8.  Migratory stroke-like lesions in a case of adult-onset mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome and a review of imaging findings.

Authors:  Stephen S Cai; Rainer von Coelln; Theresa J Kouo
Journal:  Radiol Case Rep       Date:  2016-10-05

9.  Quantitative measurement of cerebral oxygen extraction fraction using MRI in patients with MELAS.

Authors:  Lei Yu; Sheng Xie; Jiangxi Xiao; Zhaoxia Wang; Xiaodong Zhang
Journal:  PLoS One       Date:  2013-11-08       Impact factor: 3.240

Review 10.  The mitochondrial brain: From mitochondrial genome to neurodegeneration.

Authors:  Helen E Turnbull; Nichola Z Lax; Daria Diodato; Olaf Ansorge; Doug M Turnbull
Journal:  Biochim Biophys Acta       Date:  2009-08-06
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