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 diffusionweighted 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.
| Original language | English |
|---|---|
| Pages (from-to) | 1389-1392 |
| Number of pages | 4 |
| Journal | Internal Medicine |
| Volume | 52 |
| Issue number | 12 |
| DOIs | |
| State | Published - 2013 |
| Externally published | Yes |
ASJC Scopus Subject Areas
- Internal Medicine
Keywords
- L-arginine
- Lactic acidosis
- Mitochondrial encephalopathy
- Reversible cerebral vasoconstriction syndrome
- Stroke-like episode
Fingerprint
Dive into the research topics of 'MELAS and reversible vasoconstriction of the major cerebral arteries'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS