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Epistaxis and Intradural-Extramedullary Haemorrhage in a Dog With Steroid Responsive Meningitis-Arteritis.
Vet Med Sci
January 2025
Veterinary Specialists Scotland, Part of Linnaeus Veterinary Ltd., Livingston, UK.
Article Synopsis
- A 2-year-old female Golden Retriever exhibited sudden non-ambulatory paraparesis after initially unremarkable examinations, prompting further investigation.
- MRI revealed an intradural-extramedullary mass causing significant spinal cord compression, indicating a hemorrhagic process, and CSF analysis showed signs of inflammation.
- Following surgery for decompression, the dog showed gradual improvement and regained mobility, and the diagnosis of steroid responsive meningitis-arteritis (SRMA) was supported by clinical findings and treatment response.
Orbital Apex Venous Malformation: Case Report on an Unusual Clinical and Radiological Presentation.
Ophthalmic Plast Reconstr Surg
December 2024
South Australian Institute of Ophthalmology, Royal Adelaide Hospital, Adelaide.
The authors present a case of an orbital apex venous malformation that presented with an intermittent oculomotor nerve palsy over a 15-year period. Radiologically, the lesion presented as a well-circumscribed orbital mass with T2 hyperintensity and enhancement that could only be demonstrated on 2-hour delayed phase imaging. The venous malformation was initially steroid-responsive but eventually became refractory to medical treatment alone.
View Article and Find Full Text PDFChildhood-onset focal epilepsy and acute para-infectious encephalopathy in a patient with biallelic QARS1 variants.
Neurol Sci
December 2024
Neurophysiopathology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Introduction: Biallelic variants in QARS1, a house-keeping gene involved in protein synthesis, cause a rare encephalopathy classically characterized by severe developmental delay, drug-resistant neonatal-onset epilepsy, microcephaly, and brain atrophy. We aim to raise awareness on mild QARS1-related phenotypes describing a 6-year-old patient.
Case Description: Epilepsy onset occurred at 3.
A Challenging Diagnosis of Steroid-Responsive Encephalopathy Associated With Autoimmune Thyroiditis (SREAT) in a Systemic Lupus Erythematosus (SLE) Patient With Hashimoto Encephalopathy (HE): A Case Report.
Cureus
November 2024
Neurology, Sheikh Khalifa Medical City, Abu Dhabi, ARE.
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare condition that can present with multiple neurological and psychiatric manifestations. SREAT diagnosis poses a challenge due to the nature of its nonspecific symptomatology and its overlap with numerous autoimmune, metabolic, infectious, and neuropsychiatric disorders. It is associated with elevated anti-thyroid antibodies, occurs in correspondence with autoimmune thyroiditis, and shows great response to corticosteroid treatment.
View Article and Find Full Text PDFSpinal shock in a dog with steroid-responsive meningitis-arteritis extending to the brainstem.
J Small Anim Pract
November 2024
Department of Clinical Sciences, Royal Veterinary College, Hatfield, UK.
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