| Literature DB >> 33300189 |
Yuichi Hayashi1, Yasushi Iwasaki2, Nobuaki Yoshikura1, Megumi Yamada1, Akio Kimura1, Takashi Inuzuka1,3, Hiroaki Miyahara2, Yuichi Goto4, Ichizo Nishino5, Mari Yoshida2, Takayoshi Shimohata1.
Abstract
We report clinicopathological findings of a patient with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes/Leigh syndrome (MELAS/LS) associated with a novel m.3482A>G mutation in MT-ND1. A 41-year-old woman had experienced multiple stroke-like episodes since age 16. She developed akinetic mutism two months before admission to our hospital. Neurological examination revealed akinetic mutism, bilateral deafness, and muscular atrophy. Cerebrospinal fluid tests revealed elevated pyruvate and lactate levels. Fluid-attenuated inversion recovery images on magnetic resonance imaging showed hyperintense areas in the right frontal and both sides of temporal and occipital lobes, both sides of the striatum, and the midbrain. Muscle biopsy revealed strongly succinate dehydrogenase-reactive blood vessels. L-arginine therapy improved her consciousness and prevented further stroke-like episodes. However, she died from aspiration pneumonia. Postmortem autopsy revealed scattered infarct-like lesions with cavitation in the cerebral cortex and necrotic lesions in the striatum and midbrain. The patient was pathologically confirmed as having MELAS/LS based on two characteristic clinicopathological findings: presenting MELAS/LS overlap phenotype and effectiveness of L-arginine treatment.Entities:
Keywords: L-arginine; Leigh syndrome; MELAS; MT-ND1 gene; mitochondrial encephalopathy
Year: 2020 PMID: 33300189 DOI: 10.1111/neup.12709
Source DB: PubMed Journal: Neuropathology ISSN: 0919-6544 Impact factor: 1.906