Publications by authors named "Marioni-Henry K"

Background: Spinal arachnoid diverticulum (SAD) is considered a rare disease in cats. Previous reports mainly classified SAD in cats as acquired.

Hypothesis/objectives: The aim of this study was to describe the signalment, clinical presentation, diagnostic imaging findings, and outcome in a group of cats with SAD.

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  • Diffuse pachymeningeal contrast enhancement in dogs is rare and not well understood in veterinary medicine.
  • A 2-year-old neutered female Pug exhibited severe neurological symptoms and MRI revealed thickening and enhancement of the meninges.
  • Despite initial treatment showing temporary improvement, the dog relapsed multiple times, leading to euthanasia, where histopathological analysis indicated a rare case of meningeal null cell lymphoma.
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Background: This study aimed to identify complications associated with cerebrospinal fluid (CSF) collection in dogs.

Methods: This was a prospective, observational multicentre study using data collected from 102 dogs undergoing CSF collection for the investigation of neurological disease. CSF was collected from the cerebellomedullary cistern (CMC), lumbar subarachnoid space (LSAS) or both sites.

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Background: Bruxism is a repetitive masticatory muscle activity characterized by clenching or grinding of the teeth, or by bracing or thrusting of the mandible, or both.

Objectives: To investigate whether bruxism in awake dogs could be associated with brain lesions.

Animals: Four dogs with episodic bruxism in the awake state.

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Cerebrospinal fluid (CSF) collection from the cerebellomedullary cistern (CM) of dogs with congenital or acquired cerebellar herniation could lead to serious complications. It is anecdotally more challenging in large brachycephalic breeds possibly due to the increased distance between the skin and CM. The first objective of this study was to assess whether flexed-neck sagittal magnetic resonance imaging (MRI) sequences would assist in the decision-making process of collecting CSF from the CM.

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In collaboration with the American College of Veterinary Radiology.

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Background: Gliomas in dogs remain poorly understood.

Objectives: To characterize the clinicopathologic findings, diagnostic imaging features and survival of a large sample of dogs with glioma using the Comparative Brain Tumor Consortium diagnostic classification.

Animals: Ninety-one dogs with histopathological diagnosis of glioma.

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Case Summary: A 4-month-old male entire domestic shorthair cat presented for sudden onset of right thoracic monoparesis following a fall; within 18 h, the clinical signs progressed to non-ambulatory right hemiplegia with absent sensation in the distal right thoracic limb and left hemiparesis. MRI revealed changes consistent with a C6-C7 acute non-compressive nucleus pulposus extrusion with suspected secondary C5-C7 spinal cord haemorrhage. Rehabilitation exercises were started immediately after the diagnosis of acute spinal cord trauma.

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  • The collage VI-related muscular dystrophies in humans vary in severity from conditions like Ullrich congenital muscular dystrophy to milder forms such as Bethlem myopathy, characterized by muscle weakness and joint issues.
  • These conditions impact both muscle and connective tissue, leading to symptoms like respiratory failure, joint hyperlaxity, and contractures.
  • Researchers have identified two specific COL6A3 mutations in Labrador Retrievers that cause similar congenital myopathies, showcasing parallels between the diseases in dogs and humans.
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Background: Middle ear effusion is common in brachycephalic dogs with similarities to otitis media with effusion in children. Association with the cranial and eustachian tube morphology and bacterial infection is suspected in both species.

Hypothesis/objectives: To determine cytological and bacteriological features of middle ear effusions in dogs, provide information on histological features, and further assess the dog as a model of the human disease.

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Structural 'brain age' is a valuable but complex biomarker for several brain disorders. The dog is an unrivalled comparator for neurological disease modeling, however canine brain morphometric diversity creates computational and statistical challenges. Using a data-driven approach, we explored complex interactions between patient metadata, brain morphometry, and neurological disease.

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  • A 9-year-old male cat presented with lethargy and pain for three weeks, leading to an MRI revealing a large mass affecting the nasal cavity and brain.
  • The mass was found to be a transitional meningioma, causing significant complications like herniation and cribriform plate destruction.
  • This case is notable as it is the first report of a meningioma in a cat with considerable nasal involvement, suggesting it should be considered in similar cases.
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In this pilot study we investigated the expression of 14 microRNAs in the cerebrospinal fluid (CSF) of dogs with neoplastic, inflammatory and degenerative disorders affecting the central nervous system (CNS). CSF microRNA (miRNA) expression profiles were compared to those from dogs with neurological signs but no evidence of structural or inflammatory CNS disease. Seven miRNAs were easily detected in all samples: miR-10b-5p, miR-19b, miR-21-5p, miR-30b-5p, miR-103a-3p, miR-124, and miR-128-3p.

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Case Series Summary: This was a retrospective study on the clinical features and response to treatment in seven cats with feline hyperaesthesia syndrome (FHS) and tail mutilation. FHS is a poorly understood disorder characterised by skin rippling over the dorsal lumbar area, episodes of jumping and running, excessive vocalisation, and tail chasing and self-trauma. The majority of the cats were young, with a median age of 1 year at the onset of clinical signs, male (n = 6) and with access to the outdoors (n = 5).

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Background: Hypophysitis is an umbrella term for a group of disorders involving inflammation of the pituitary gland. A rare occurrence in humans, hypophysitis can produce a range of clinical signs including (but not limited to) visual deficits and diabetes insipidus. Only five cases of canine hypophysitis exist in the literature, all presenting in mature dogs with no visual deficits and a grave outcome.

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A dog presented with a retrobulbar mass, diagnosed histopathologically as malignant spindle cell neoplasia. Emergence of analogous findings in the contralateral orbit prompted extended immunohistochemistry of the original mass and reassignment to idiopathic sclerosing orbital inflammation. Early incisional biopsy with extended immunohistochemical analysis should be considered for canine orbital tumors.

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  • Anecdotal reports of involuntary movement episodes in Border Terriers suggest a possible link to paroxysmal dystonic choreoathetosis, prompting a study to analyze this condition's characteristics and clinical progression.
  • Data were collected from veterinary neurologists and affected dog owners, revealing that the episodes often feature dystonia, tremors, and can be triggered by excitement, with some owners noting improvements through dietary changes.
  • The research indicates a potential genetic predisposition to this dystonia phenotype, highlighting the need for further exploration into its genetic causes and effective treatment options using anticonvulsants and dietary adjustments.
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Objective: To report the clinical, imaging, pathologic findings, surgical planning, and long-term outcome after surgery in a dog with neurologic deficits because of a hypertrophic ganglioneuritis that compressed the spinal cord.

Study Design: Clinical report.

Animal: An 8-year-old male intact Yorkshire terrier.

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