| Literature DB >> 23774553 |
Takeshi Yoshida1, Atsushi Ouchi, Daisuke Miura, Kunihiro Shimoji, Kazushi Kinjo, Takeshi Sueyoshi, Manabu Jonosono, Vijay Rajput.
Abstract
A 26-year-old woman was admitted due to an altered mental status and generalized tonic-clonic seizures. She had experienced chronic migraine-like headaches, progressive bilateral hearing loss, a short stature and nephrotic syndrome. Laboratory data showed elevated lactate and pyruvate levels. Brain MRI using diffusion-weighted imaging revealed a hyperintense lesion in the left temporal lobe. MR angiography revealed segmental stenosis at the C1 and M1-2 junction. A genetic study revealed a mitochondrial DNA A3243G point mutation. The patient's clinical symptoms and MRI/MR angiography (MRA) findings improved within four weeks. We herein discuss the possible pathophysiology involving both stroke-like episodes and reversible vasoconstriction.Entities:
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Year: 2013 PMID: 23774553 DOI: 10.2169/internalmedicine.52.0188
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271