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一只患有癫痫的成年猫的丹迪-沃克样畸形:临床描述及MRI特征

Dandy Walker-like malformation in an adult cat with seizures: clinical description and MRI characteristics.

作者信息

Formoso Sara, Padley Hannah, Alves Lisa

机构信息

Department of Small Animal Medicine, Queen's Veterinary School Hospital, University of Cambridge, Cambridge, UK.

Anderson Moores Veterinary Specialists, Hursley, Hampshire, UK.

出版信息

JFMS Open Rep. 2023 Jun 23;9(1):20551169231174199. doi: 10.1177/20551169231174199. eCollection 2023 Jan-Jun.

DOI:10.1177/20551169231174199
PMID:37378378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10291414/
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, serology and 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.

摘要

病例摘要

一只2岁已绝育的雄性家养短毛猫因有10个月自限性全身性强直阵挛性癫痫发作病史而被转诊进行检查。据报告,这只猫在发作间期正常,但一直存在静态异常步态。全身体格检查无异常。神经解剖定位与弥漫性小脑和弥漫性前脑病变相符。全血细胞计数、生化检查、胆汁酸刺激试验、尿液分析、脑池脑脊液(CSF)分析、血清学检查以及脑脊液中的聚合酶链反应均无异常。磁共振成像(MRI)显示后颅窝异常,小脑蚓部缺如,小脑半球小,第四脑室扩张。在MRI或脑脊液变化中未发现可解释癫痫发作的前脑异常。考虑到临床表现、猫的神经系统检查和MRI特征,做出了疑似丹迪-沃克样畸形(DWLM)和病因不明的癫痫的诊断。

相关性及新信息

这是首例成年猫被诊断为类似DWLM的小脑畸形并伴有癫痫发作、其MRI特征及长期随访的病例报告。3年的随访会诊显示神经状态稳定,每年发作2 - 4次癫痫。在撰写本文时,这只猫的生活质量仍然良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/790c85856167/10.1177_20551169231174199-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/167a6b1d9dd0/10.1177_20551169231174199-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/7407e2f3573d/10.1177_20551169231174199-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/0fe09f0c6bdd/10.1177_20551169231174199-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/b9e8ebffec58/10.1177_20551169231174199-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/790c85856167/10.1177_20551169231174199-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/167a6b1d9dd0/10.1177_20551169231174199-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/7407e2f3573d/10.1177_20551169231174199-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/0fe09f0c6bdd/10.1177_20551169231174199-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/b9e8ebffec58/10.1177_20551169231174199-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7559/10291414/790c85856167/10.1177_20551169231174199-fig5.jpg

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