Peer-reviewed veterinary case report
Symptomatic Narcolepsy/Cataplexy in a Dog with Brainstem Meningoencephalitis of Unknown Origin.
- Journal:
- Journal of the American Animal Hospital Association
- Year:
- 2020
- Authors:
- Mari, Lorenzo & Shea, Anita
- Affiliation:
- From the Neurology/Neurosurgery Service · United Kingdom
- Species:
- dog
Plain-English summary
A 4-year-old female cocker spaniel was brought to the vet because she was very tired and had episodes of sudden weakness, along with some balance issues. During her check-up, she had a narcolepsy-cataplexy episode, which is when a dog suddenly loses muscle control, and this caused her heart rate to drop and blood pressure to rise. Tests, including blood work and imaging, didn’t show any obvious problems, but an MRI and spinal fluid analysis indicated inflammation in her brain. She started treatment with medications to suppress her immune system, and over three weeks, her episodes became less frequent and eventually stopped completely, with no signs of relapse over the next 32 months. The treatment was successful, and follow-up tests showed significant improvement.
Abstract
A 4 yr old, intact female cocker spaniel was presented for investigation of acute, progressive lethargy/hypersomnia; vestibular signs; and cataplexy. A narcolepsy-cataplexy episode with associated hypertension and bradycardia was triggered during examination. There was no evidence of arrhythmia on electrocardiography during the episode. Hematology, serum biochemistry, and thoracic and abdominal imaging were unremarkable. MRI of the brain and cerebrospinal fluid analysis were compatible with meningoencephalitis of unknown origin affecting the mesencephalon, pons and rostral medulla oblongata. The dog was started on immunosuppressive treatment with prednisolone and cytosine arabinoside, which was subsequently switched to cyclosporine. Narcolepsy-cataplexy episodes could initially still be triggered by offering food; however, they gradually became shorter and less frequent until they completely subsided along with all other clinical signs after 3 wk. No relapse occurred over a 32 mo follow-up period from the diagnosis. Repeated MRI revealed marked reduction in the lesion size; cerebrospinal fluid analysis revealed no abnormalities. Although very rare, symptomatic narcolepsy/cataplexy can occur in dogs and can be secondary to brainstem encephalitis. Cardiovascular changes can occur in association with narcolepsy/cataplexy and should be considered when dealing with patients presenting with these specific clinical signs.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/31961221/