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We report a 59-year-old immunocompetent man presenting with slowly progressive gait unsteadiness, dysarthria, and clumsiness in writing over 6 months. There were bilateral pyramidal signs, pseudobulbar palsy, and attention deficits. Cerebrospinal fluid examination showed mild mononuclear pleocytosis, and magnetic resonance imaging revealed pachymeningeal pattern of contrast enhancement beneath the calvarium and the posterior cranial fossa.

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["Ephedron" encephalopathy].

Zh Nevrol Psikhiatr Im S S Korsakova

October 2005

The results of clinical, neuropsychological and MRI study of 21 patients with "ephedron" encephalopathy caused by intake of methcatinon ("ephedron"), a surrogate drug obtained from phenylpropanolamine-containing compounds by adding potassium permanganate, are presented. Signs of brain lesions emerged 3-14 (mean 6.8 +/- 4.

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48-year-old left-handed man experienced a sudden loss of taste, followed by dysarthria and dysphagia. Taste threshold examined by a small filter-paper disc method was severely elevated on both sides of the tongue. Brain CT revealed right putaminal hemorrhage that measured 9.

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[Paucisymptomatic and reversible myelinolysis after an anaphylactic shock].

Rev Neurol (Paris)

November 2002

Service de Neurologie, CHU Henri MONDOR, Créteil, France.

Article Synopsis
  • - Myelinolysis is a type of demyelination primarily affecting the central part of the pons, leading to symptoms like spastic tetraparesis and pseudobulbar paralysis.
  • - The case study involves a 58-year-old man who experienced pontine and extrapontine myelinolysis following an anaphylactic shock, despite not having low sodium levels (hyponatremia).
  • - The patient's condition improved over a few days, and MRI results normalized within three months, suggesting that mild myelinolysis can resolve on its own after a shock event.
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We examined the alterations of glial cells in the brains with Binswanger's disease. In comparison to the brains with lacunar cerebral infarction and those from non-neurological controls, oligodendroglia was decreased in number, and microglia was increased and activated in the white matter lesions in Binswanger's disease. Astroglia occasionally showed a regressive change, termed clasmatodendrosis.

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