{"title":"Dandy Walker-like malformation in an adult cat with seizures: clinical description and MRI characteristics.","authors":"Sara Formoso, Hannah Padley, Lisa Alves","doi":"10.1177/20551169231174199","DOIUrl":null,"url":null,"abstract":"<p><strong>Case summary: </strong>A 2-year-old male neutered domestic shorthair cat was referred for investigation of a 10-month history of self-limiting, generalised tonic-clonic seizures. The cat was reported to be normal interictally but had always had a static abnormal gait. General physical examination was unremarkable. Neuroanatomical localisation was compatible with a diffuse cerebellar and diffuse forebrain lesion. Complete blood count, biochemistry, bile acid stimulation test, urinalysis, cisternal cerebrospinal fluid (CSF) analysis, <i>Toxoplasma gondii</i> serology and <i>T gondii</i> polymerase chain reaction in CSF were all unremarkable. MRI revealed an abnormal caudal fossa, absent cerebellar vermis and small cerebellar hemisphere with distension of the fourth ventricle. There were no forebrain abnormalities identified in the MRI or CSF changes that could justify the seizures. Considering the clinical presentation, the cat's neurological examination and MRI features, a presumptive diagnosis of Dandy Walker-like malformation (DWLM) and epilepsy of unknown aetiology was made.</p><p><strong>Relevance and novel information: </strong>This is the first case report of an adult cat diagnosed with cerebellar malformation resembling DWLM and concomitant seizures, its MRI characteristics and long-term follow-up. The 3-year follow-up consultation revealed static neurological status with 2-4 seizures per year. The cat's quality of life remained good at the time of writing.</p>","PeriodicalId":36588,"journal":{"name":"Journal of Feline Medicine and Surgery Open Reports","volume":"9 1","pages":"20551169231174199"},"PeriodicalIF":0.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291414/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Feline Medicine and Surgery Open Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20551169231174199","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Case summary: A 2-year-old male neutered domestic shorthair cat was referred for investigation of a 10-month history of self-limiting, generalised tonic-clonic seizures. The cat was reported to be normal interictally but had always had a static abnormal gait. General physical examination was unremarkable. Neuroanatomical localisation was compatible with a diffuse cerebellar and diffuse forebrain lesion. Complete blood count, biochemistry, bile acid stimulation test, urinalysis, cisternal cerebrospinal fluid (CSF) analysis, Toxoplasma gondii serology and T gondii polymerase chain reaction in CSF were all unremarkable. MRI revealed an abnormal caudal fossa, absent cerebellar vermis and small cerebellar hemisphere with distension of the fourth ventricle. There were no forebrain abnormalities identified in the MRI or CSF changes that could justify the seizures. Considering the clinical presentation, the cat's neurological examination and MRI features, a presumptive diagnosis of Dandy Walker-like malformation (DWLM) and epilepsy of unknown aetiology was made.
Relevance and novel information: This is the first case report of an adult cat diagnosed with cerebellar malformation resembling DWLM and concomitant seizures, its MRI characteristics and long-term follow-up. The 3-year follow-up consultation revealed static neurological status with 2-4 seizures per year. The cat's quality of life remained good at the time of writing.
病例总结:一只2岁的雄性绝育家短毛猫被转介调查其10个月的自限性全身性强直阵挛发作史。据报道,这只猫在内部是正常的,但总是有一个静态的异常步态。全身检查无明显异常。神经解剖定位与弥漫性小脑和弥漫性前脑病变相符。全血计数、生化、胆汁酸刺激试验、尿液分析、池脑脊液分析、刚地弓形虫血清学及脑脊液中刚地弓形虫聚合酶链反应均无显著差异。MRI显示尾侧窝异常,小脑蚓部缺失,小脑半球小,第四脑室肿胀。MRI检查中未发现前脑异常或脑脊液变化,证明癫痫发作是合理的。考虑到猫的临床表现、神经学检查和MRI特征,推定诊断为丹迪·沃克样畸形(Dandy walker like mal畸形,DWLM)和病因不明的癫痫。相关性和新信息:这是第一例被诊断为小脑畸形的成年猫,类似DWLM并伴有癫痫发作,其MRI特征和长期随访。3年随访咨询显示神经系统状态稳定,每年2-4次癫痫发作。在撰写本文时,这只猫的生活质量仍然很好。