| Literature DB >> 25128282 |
Shoko Minobe1, Akiko Matsuda1, Tetsuya Mitsuhashi1, Motonao Ishikawa1, Yoshiko Nishimura1, Koichi Shibata2, Eiichi Ito3, Yu-ichi Goto4, Takashi Nakaoka1, Hiroshi Sakura1.
Abstract
We describe a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS), with multiple cerebral vasodilatations in a stroke-like episode visualised by using magnetic resonance angiography (MRA) and CT angiography (CTA). In the acute stroke-like episode stage, T2-weighted and fluid-attenuated inversion recovery MRI showed high-intensity areas in the left occipital area. In addition, MRA and CTA revealed prominent dilatation of the left posterior cerebral artery and temporal branches of the middle cerebral artery with focal hyperperfusions using CT perfusion (CTP) that corresponded to the MRI. After 10 days, with the development of aphasia, MRI indicated the lesions had spread to the temporal and parietal regions, and this distribution was not confined to major vascular territories. The patient's symptoms gradually improved, accompanied by the attenuation of MRI, CTA, and CTP findings. These characteristic features along with the MRI changes that spread beyond vascular boundaries and the multiple cerebral vasodilatations prior to the development of clinical symptoms are not fully explained by the mitochondrial angiopathy or cytopathy theories. These findings provide further evidence supporting neuronal hyperexcitability in stroke-like episodes of MELAS.Entities:
Keywords: CTA; MELAS; MRA; Stroke-like episode; Vasodilatation
Mesh:
Year: 2014 PMID: 25128282 DOI: 10.1016/j.jocn.2014.05.021
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961