[Conventional and diffusion-weighted magnetic resonance imaging and proton spectroscopy in MELAS]
- PMID: 23177587
[Conventional and diffusion-weighted magnetic resonance imaging and proton spectroscopy in MELAS]
Abstract
Introduction: MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) is a mitochondrial hereditary dysfunction in which the physiopathological mechanism of cerebral lesions is not totally understood as yet. Typically, these lesions are described as having normal to increased apparent diffusion coefficient (ADC), and this has been used to distinguish stroke-like lesions from ischemic lesions. Notwithstanding this, within the last few years, there have been reports of diffusion restriction in stroke-like episodes.
Objectives: Analysis of the diffusion characteristics on serial magnetic resonance imaging (MRI) over a 16 month period, on a patient with MELAS and stroke-like lesions, to investigate the controversial changes of the ADC, reported in the last years. Evaluation of the proton spectroscopy changes in stroke-like lesions and apparently spared brain.
Methods: We performed four serial magnetic resonance imaging (MRI), including two stroke-like episodes, in a 28-year-old man with MELAS (mitochondrial DNA mutation A3243G). Qualitative analysis of the magnetic resonance images, including the single voxel spectroscopy and ADC maps, with analysis of evolution patterns of the last ones.
Results: Both MRI that were performed during those episodes of stroke-like lesion revealed areas of diffusion restriction, coexisting areas of high ADC. During the chronic phase, there was a regression of those changes. Proton spectroscopy showed the presence of lactate and reduction of N-acetyl aspartate peak in stroke-like lesion and the presence of lactate in apparently spared brain.
Conclusions: All alterations that were recorded strengthen the view that cytotoxic oedema can occur in stroke-like lesions. Thus, their presence should not weaken the possibility of MELAS, especially if those lesions affect the temporal, parietal and/or occipital lobes, or if they predominantly involve the cortical gray matter, spanning vascular borders and if proton spectroscopy reveals lactate peak in the apparently spared brain.
Similar articles
-
Serial brain imaging analysis of stroke-like episodes in MELAS.Brain Dev. 2008 Aug;30(7):483-8. doi: 10.1016/j.braindev.2008.01.003. Epub 2008 Mar 4. Brain Dev. 2008. PMID: 18289816
-
Neuroimaging of stroke-like episodes in MELAS.Brain Dev. 2011 Apr;33(4):283-8. doi: 10.1016/j.braindev.2010.06.010. Epub 2010 Jul 6. Brain Dev. 2011. PMID: 20609541 Review.
-
Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.Stroke. 2009 Feb;40(2):e15-7. doi: 10.1161/STROKEAHA.108.523118. Epub 2008 Dec 18. Stroke. 2009. PMID: 19095975
-
Can diffusion weighted magnetic resonance imaging help differentiate stroke from stroke-like events in MELAS?J Neurol Neurosurg Psychiatry. 2000 Aug;69(2):248-50. doi: 10.1136/jnnp.69.2.248. J Neurol Neurosurg Psychiatry. 2000. PMID: 10896703 Free PMC article.
-
Diffusion-weighted MR of the brain: methodology and clinical application.Radiol Med. 2005 Mar;109(3):155-97. Radiol Med. 2005. PMID: 15775887 Review. English, Italian.
Cited by
-
MRI Features of Stroke-Like Episodes in Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes.Front Neurol. 2022 Feb 9;13:843386. doi: 10.3389/fneur.2022.843386. eCollection 2022. Front Neurol. 2022. PMID: 35222261 Free PMC article. Review.
-
In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.Neurochem Res. 2015 Dec;40(12):2647-85. doi: 10.1007/s11064-015-1772-1. Epub 2015 Nov 26. Neurochem Res. 2015. PMID: 26610379 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources