Results 41 to 50 of about 3,947 (209)

Tumefactive demyelination: Clinical outcomes, lesion evolution and treatments

open access: yesMultiple Sclerosis Journal - Experimental, Translational and Clinical, 2019
Objective Large demyelinating lesions with possible mass effect (tumefactive multiple sclerosis or tumefactive demyelination) can be mistaken for tumour-like space-occupying lesions suggesting a malignant outcome.
Staley A Brod   +2 more
doaj   +1 more source

Stroke Mimicry: Unmasking a Brainstem Tuberculoma in a Young Patient. [PDF]

open access: yesClin Case Rep
A young male presented with stroke‐like symptoms ‐ progressive hemiparesis and cranial nerve palsies. MRI brain revealed a ring‐enhancing intrapontine lesion with perilesional edema, suggestive of tuberculoma. Early initiation of anti‐tubercular therapy led to complete recovery.
Palanisamy NN   +5 more
europepmc   +2 more sources

Immunopathology of Tumefactive Demyelinating Lesions-From Idiopathic to Drug-Related Cases

open access: yesFrontiers in Neurology, 2022
Tumefactive demyelinating lesions (TDL) represent a diagnostic dilemma for clinicians, and in rare atypical cases a collaboration of a neuroradiologist, a neurologist, and a neuropathologist is warranted for accurate diagnosis.
Aigli G. Vakrakou   +5 more
doaj   +1 more source

IgG4-related Renal Disease Case Report and Review of Literature

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth
IgG4-related disease (IgG4-RD) is a clinical entity that involves multiple organs and is characterized by high levels of serum IgG4. We present a case of an elderly male reporting fatigue and weight loss, who after extensive workup, was diagnosed as a ...
Arijit Sen   +3 more
doaj   +1 more source

Neuromyelitis Optica Spectrum Disorder with Tumefactive Demyelination mimicking Multiple Sclerosis: a rare case

open access: yesFrontiers in Neurology, 2016
Neuromyelitis optica spectrum disorder (NMOSD) is a diverse condition which not only encompasses isolated longitudinally extensive transverse myelitis and optic neuritis but also includes area postrema syndrome, acute brainstem syndrome, symptomatic ...
UJJAWAL eROY   +5 more
doaj   +1 more source

Tumefactive neuro-Behçet disease [PDF]

open access: yesNeurology, 2004
A man aged 23 years, with a previous clinical diagnosis of Behcet disease (recurrent genital and oral ulceration and papulopustular rash), sought treatment for a 3-week history of headache, fever, and progressive right-sided weakness. Clinical examination revealed a right homonymous hemianopia and …
Bennett, D.L.H.   +5 more
openaire   +2 more sources

Tumefactive multiple sclerosis plaque [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 2002
We present a case of a large solitary demyelinating plaque in the brain masquerading as tumour. A 34 year old healthy woman presented with sudden onset of left hemiparesis. Subsequent MRI of the brain showed a single large 2.5 cm right sided enhancing lesion within the white matter of the parietal lobe …
S, Khoshyomn, S P, Braff, P L, Penar
openaire   +2 more sources

Sinonasal immunoglobin G4—related disease: case report and review

open access: yesClinical Case Reports, 2021
Immunoglobin G4—related disease (IgG4‐RD) is a chronic fibro‐inflammatory condition that presents as a single or multiple tumefactive lesions affecting virtually any organ system.
Caleb P. Wilson   +3 more
doaj   +1 more source

Deep and disseminated dermatophytosis in immunocompromised populations—A systematic review

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Dermatophyte infections of the dermis and subcutaneous tissue (i.e. deep dermatophytosis)—associated with secondary complications including pseudomycetoma and systemic dissemination—affect vulnerable populations with primary or acquired immunodeficiencies.
Aditya K. Gupta   +5 more
wiley   +1 more source

Mutation in RNF170 Causes Unsteady Gait with Hypertrophic Olivary Degeneration

open access: yesClinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration resulting from disruption of the Guillain–Mollaret triangle, typically presenting with palatal tremor, ataxia, and nystagmus. Mutations in the Ring Finger Protein 170 (RNF170) gene have been associated with autosomal dominant sensory ataxia.
Change Wang
wiley   +1 more source

Home - About - Disclaimer - Privacy