João Miguel De Frias, Sofie F. M. Bhatti, George Nye, Rita Gonçalves, Tom Harcourt-Brown, Angela Fadda, Katia Marioni-Henry, Hannah Padley, Steven De Decker
{"title":"猫的脊髓蛛网膜憩室:临床表现、诊断影像表现、治疗和结果。","authors":"João Miguel De Frias, Sofie F. M. Bhatti, George Nye, Rita Gonçalves, Tom Harcourt-Brown, Angela Fadda, Katia Marioni-Henry, Hannah Padley, Steven De Decker","doi":"10.1111/jvim.17294","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Spinal arachnoid diverticulum (SAD) is considered a rare disease in cats. Previous reports mainly classified SAD in cats as acquired.</p>\n </section>\n \n <section>\n \n <h3> Hypothesis/Objectives</h3>\n \n <p>The aim of this study was to describe the signalment, clinical presentation, diagnostic imaging findings, and outcome in a group of cats with SAD.</p>\n </section>\n \n <section>\n \n <h3> Animals</h3>\n \n <p>Twenty-one client-owned cats.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Multicenter observational retrospective review of the medical records of cats diagnosed with SAD by magnetic resonance imaging.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Most cats were Domestic Short Hair (67%), male (63%), and had a wide range of ages (18 weeks to 13 years old). Neuroanatomical localization was consistent with a T3-L3 myelopathy in 18 cats (86%) and C1-C5 myelopathy in 3 cats (14%). One cat with a C1-C5 myelopathy demonstrated bilateral vestibular clinical signs. One cat (5%) had fecal incontinence. Most cats demonstrated a chronic, progressive, nonlateralized, nonpainful myelopathy. No underlying previous or concurrent spinal condition was found in 48% of the cats. No difference in age, body weight, breed, sex, treatment, or outcome was found between cats with or without a concurrent spinal disorder. One cat was euthanized after diagnosis. Six cats improved, 1 deteriorated and 1 remained static after surgery, whereas 3 cats improved, 5 deteriorated and 4 remained static after medical management on the short-term outcome. Overall, 73% (8/11) of the cats deteriorated on available long-term follow-up information.</p>\n </section>\n \n <section>\n \n <h3> Conclusions and Clinical Importance</h3>\n \n <p>Spinal arachnoid diverticulum should be considered for cats with chronic, progressive, symmetrical, nonpainful myelopathy, particularly if male and with a history of spinal disease or surgery.</p>\n </section>\n </div>","PeriodicalId":49958,"journal":{"name":"Journal of Veterinary Internal Medicine","volume":"39 1","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11683399/pdf/","citationCount":"0","resultStr":"{\"title\":\"Spinal arachnoid diverticula in cats: Clinical presentation, diagnostic imaging findings, treatment, and outcome\",\"authors\":\"João Miguel De Frias, Sofie F. M. 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Previous reports mainly classified SAD in cats as acquired.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Hypothesis/Objectives</h3>\\n \\n <p>The aim of this study was to describe the signalment, clinical presentation, diagnostic imaging findings, and outcome in a group of cats with SAD.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Animals</h3>\\n \\n <p>Twenty-one client-owned cats.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Multicenter observational retrospective review of the medical records of cats diagnosed with SAD by magnetic resonance imaging.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Most cats were Domestic Short Hair (67%), male (63%), and had a wide range of ages (18 weeks to 13 years old). Neuroanatomical localization was consistent with a T3-L3 myelopathy in 18 cats (86%) and C1-C5 myelopathy in 3 cats (14%). One cat with a C1-C5 myelopathy demonstrated bilateral vestibular clinical signs. 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Spinal arachnoid diverticula in cats: Clinical presentation, diagnostic imaging findings, treatment, and outcome
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.
Animals
Twenty-one client-owned cats.
Methods
Multicenter observational retrospective review of the medical records of cats diagnosed with SAD by magnetic resonance imaging.
Results
Most cats were Domestic Short Hair (67%), male (63%), and had a wide range of ages (18 weeks to 13 years old). Neuroanatomical localization was consistent with a T3-L3 myelopathy in 18 cats (86%) and C1-C5 myelopathy in 3 cats (14%). One cat with a C1-C5 myelopathy demonstrated bilateral vestibular clinical signs. One cat (5%) had fecal incontinence. Most cats demonstrated a chronic, progressive, nonlateralized, nonpainful myelopathy. No underlying previous or concurrent spinal condition was found in 48% of the cats. No difference in age, body weight, breed, sex, treatment, or outcome was found between cats with or without a concurrent spinal disorder. One cat was euthanized after diagnosis. Six cats improved, 1 deteriorated and 1 remained static after surgery, whereas 3 cats improved, 5 deteriorated and 4 remained static after medical management on the short-term outcome. Overall, 73% (8/11) of the cats deteriorated on available long-term follow-up information.
Conclusions and Clinical Importance
Spinal arachnoid diverticulum should be considered for cats with chronic, progressive, symmetrical, nonpainful myelopathy, particularly if male and with a history of spinal disease or surgery.
期刊介绍:
The mission of the Journal of Veterinary Internal Medicine is to advance veterinary medical knowledge and improve the lives of animals by publication of authoritative scientific articles of animal diseases.