The case of a 25-year old man who presented with meningoencephalitis as the sole clinical manifestation of Q fever is described. Serological studies revealed the presence of IgM and IgG antibodies to Coxiella burnetii. The patient responded favourably to a ten-day course of i.v. ceftriaxone and was discharged without any neurological sequelae.
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http://dx.doi.org/10.1007/BF01997054 | DOI Listing |
Case Rep Neurol
October 2024
Department of Neurology, Institute of Medical Sciences Banaras Hindu University, Varanasi, India.
Front Microbiol
July 2024
The Michael Smith Laboratories, University of British Columbia, Vancouver, BC, Canada.
mBio
June 2024
Department of Microbiology, University of Georgia, Athens, Georgia, USA.
Unlabelled: causes cryptococcal meningoencephalitis, a disease that kills more than 180,000 people annually. Contributing to its success as a fungal pathogen is its cell wall surrounded by a capsule. When the cryptococcal cell wall is compromised, exposed pathogen-associated molecular pattern molecules (PAMPs) could trigger host recognition and initiate attack against this fungus.
View Article and Find Full Text PDFHeadache
June 2024
Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Ictal epileptic headache, characterized by headache as the sole symptom of a seizure attack, is a rare condition. In this case report, we present a 52-year-old female with a history of systemic lupus erythematosus who sought medical attention at the headache clinic due to a new type of headache. The headache was described as an intense painful wave followed by a dull headache, without autonomic symptoms or migrainous features.
View Article and Find Full Text PDFFront Neurol
April 2024
Department of Clinical Neurological Sciences, Western University, London Health Science Center, London, ON, Canada.
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a recently emerging autoimmune disease of the central nervous system (CNS); GFAP astrocytopathy is characterized by optic neuritis and meningoencephalomyelitis. We report the case of a 55-year-old man, otherwise healthy, who presented with isolated headaches for three months, without other features of meningoencephalitis or myelitis. His neurological examination and fundoscopy were unremarkable.
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