Increased Accumulation of N-isopropyl-p-(123I)-iodoamphetamine in Two Cases with Mitochondrial Encephalomyopathy with Lactic Acidosis and Strokelike Episodes (MELAS)
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Abstract
We present two cases with mitochondrial encephalopathy with lactic acidosis and strokelike episodes (MELAS), which showed both increased and decreased accumulation of N-isopropyl-p-(123I)-iodoamphetamine (123I-IMP) in single photon emission computed tomography (SPECT). The increased accumulation of the tracer occurred, before low density appeared on conventional computed tomography, suggesting that 123I-IMP SPECT may be useful in pathophysiological study of MELAS.
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Sue C, Crimmins D, Soo Y, Pamphlett R, Presgrave C, Kotsimbos N J Neurol Neurosurg Psychiatry. 1998; 65(2):233-40.
PMID: 9703178 PMC: 2170193. DOI: 10.1136/jnnp.65.2.233.
References
1.
Kobayashi Y, Miyabayashi S, Takada G, Narisawa K, Tada K, Yamamoto T
. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis. Eur J Pediatr. 1982; 139(1):25-30.
DOI: 10.1007/BF00442074.
View
2.
Yamamoto T, Beppu H, Tsubaki T
. Mitochondrial encephalomyopathy: fluctuating symptoms and CT. Neurology. 1984; 34(11):1456-60.
DOI: 10.1212/wnl.34.11.1456.
View
3.
Kuriyama M, UMEZAKI H, Fukuda Y, Osame M, Koike K, Tateishi J
. Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions. Neurology. 1984; 34(1):72-7.
DOI: 10.1212/wnl.34.1.72.
View
4.
Nordstrom C, Rehncrona S, Siesjo B
. Restitution of cerebral energy state, as well as of glycolytic metabolites, citric acid cycle intermediates and associated amino acids after 30 minutes of complete ischemia in rats anaesthetized with nitrous oxide or phenobarbital. J Neurochem. 1978; 30(2):479-86.
DOI: 10.1111/j.1471-4159.1978.tb06553.x.
View
5.
Pavlakis S, Phillips P, DiMauro S, De Vivo D, Rowland L
. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol. 1984; 16(4):481-8.
DOI: 10.1002/ana.410160409.
View