نتایج جستجو برای: acute disseminated encephalomyelitis

تعداد نتایج: 525013  

Journal: :iranian journal of neurology 0
ferdos nazari department of neurology, school of medicine, shariati hospital, tehran university of medical sciences, tehran, iran. amirreza azimi department of neurology, school of medicine, sina hospital, tehran university of medical sciences, tehran, iran. siamak abdi department of neurology, school of medicine, shariati hospital, tehran university of medical sciences, tehran, iran.

susac's syndrome (ss) is a clinical triad of encephalopathy, branch retinal artery occlusion and sensorineural hearing loss and maybe due to an immune-mediated endotheliopathy. because of its rarity and some similarities to other common neurological conditions such as multiple sclerosis and acute disseminated encephalomyelitis, it is often misdiagnosed and therefore mistreated. to the best of o...

2016
Kensuke Daida Yuta Ishiguro Hiroto Eguchi Yutaka Machida Nobutaka Hattori Hideto Miwa

BACKGROUND It is clinically rare to find cytomegalovirus (CMV)-associated encephalomyelitis in immunocompetent adults. Here, we present the case of an adult patient who developed acute transverse myelitis that was followed by immune-mediated disseminated encephalomyelitis. CASE PRESENTATION A 38-year-old man developed acute paraplegia with paresthesia below the level of the T7-8 dermatome. Bo...

Journal: :Internal medicine 2010
Vildan Avkan-Oguz Nur Yapar Serkan Ozakbas Kubra Demir-Onder Eray Aktas Sema Alp-Cavus Sermin Ozkal Suleyman Men Aydanur Kargi

It is believed that viral infections and the hyperimmune reaction due to these infections are involved in the etiology of Kikuchi-Fujimoto Disease (KFD), a rare cause of fever of unknown origin. Axillary lymphadenopathy and neurologic involvement are rare in KFD. We present a patient diagnosed with KFD histopathologically during an investigation of the origin of fever and axillary lymphadenopat...

Journal: :Srpski Arhiv Za Celokupno Lekarstvo 2022

Introduction. Myelin oligodendrocyte glycoprotein antibody associated disorders (MOGAD) are immunemediated inflammatory conditions of the central nervous system (CNS) with a wide clinical phenotypic variability. In order to further understand possible phenotype MOGAD here we report pediatric case acute disseminated encephalomyelitis (ADEM) MOG antibodies. Case outline. A previously healthy four...

Journal: :International Journal of Contemporary Pediatrics 2023

Myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD) is an inflammatory demyelinating disorder caused by the development of immunoglobulin G autoantibody targeting MOG, which expressed exclusively on outer surface myelin sheath and plasma membrane oligodendrocyte. MOGAD can present in different clinical spectrum including acute disseminated encephalomyelitis (ADEM), optic neu...

Journal: :Pakistan Journal of Neurological Sciences 2022

Due to pervasive pandemic of SARS CoV-2 the reports rare neurological complications have turned up out ordinary. The public health concerns are raised due SARS-CoV-2 infection and vaccinations as this recent pandemics has set development deployment vaccines at large scale. randomized controlled trials being carried were underpowered foresee these adverse effects. Amongst other acute disseminate...

Journal: :International journal of research publications 2022

Pediatric optic neuritis (PON) tend to have their differences with adult (ON). It might happen due several etiologies such as neuromyelitis optica disorder, acute disseminated encephalomyelitis, multiple sclerosis and many more. While cases of post infectious vaccination rarely happened in adults compared other etiologies, it works differently on pediatric cases. ON caused a lot by vaccinations...

Journal: :Current opinion in neurology 2007
Til Menge Bernd C Kieseier Stefan Nessler Bernhard Hemmer Hans-Peter Hartung Olaf Stüve

PURPOSE OF REVIEW In this review, the possible etiology, clinical characteristics, diagnosis, and treatment of acute disseminated encephalomyelitis (ADEM) are discussed. ADEM is a para- or postinfectious autoimmune demyelinating disease of the central nervous system and has been considered a monophasic disease. The highest incidence of ADEM is observed during childhood. RECENT FINDINGS Over t...

Journal: :Osaka city medical journal 1996
T Tsutada T Izumi T Murakami

In a case of acute disseminated encephalomyelitis displaying opsoclonus-myoclonus syndrome, magnetic resonance images (MRI) disclosed pontine lesions involving part of the pontine paramedian reticular formation and the raphe nucleus. Shrinkage of the lesions correlated with the patient's clinical state. This observation supports the hypothesis that a pontine lesion can cause opsoclonus-myoclonu...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1989
R W Walker J Gawler

A 7 year old girl developed acute disseminated encephalomyelitis following a Mycoplasma pneumoniae respiratory infection. The illness followed a relapsing course during the first two months. Computed tomography (CT) showed cerebral lesions of a severity and extent out of proportion to the clinical manifestations. The CT abnormalities altered with changes in her clinical state.

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