scholarly journals SARS-CoV-2 Encephalitis Presenting as a Clinical Cerebellar Syndrome: A Case Report

Neurology ◽  
2021 ◽  
pp. 10.1212/WNL.0000000000012051
Author(s):  
Katryn Oosthuizen ◽  
Elizabeth Christina Steyn ◽  
Lawrence Tucker ◽  
Innocent Vusumusi Ncube ◽  
Diana Hardie ◽  
...  
Keyword(s):  
Case Report ◽  
Cerebellar Syndrome

scholarly journals Acute Disseminated Encephalomyelitis Following Typhoid Fever: A Case Report

2014 ◽  
Vol 9 (4) ◽  
pp. 55-58
Author(s):  
R Adhikari ◽  
A Tayal ◽  
PK Chhetri ◽  
B Pokhrel
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Case Report ◽  
Typhoid Fever ◽  
Demyelinating Disease ◽  
Acute Disseminated Encephalomyelitis ◽  
Medical Sciences ◽  
Cerebellar Syndrome ◽  
Immune Mediated ◽  
The Central Nervous System

The involvement of central nervous system in children with typhoid fever is common. Acute disseminated encephalomyelitis is a rare immune mediated and demyelinating disease of the central nervous system that usually affects children. We report a 7-year-old child with typhoid fever who developed acute cerebellar syndrome due to acute disseminated encephalomyelitis.Journal of College of Medical Sciences-Nepal, 2013, Vol-9, No-4, 55-58 DOI: http://dx.doi.org/10.3126/jcmsn.v9i4.10237

scholarly journals Epidermoid Cyst of the IV Ventricle: Case Report

2017 ◽  
Vol 39 (01) ◽  
pp. 041-045
Author(s):  
Washington Clésio da Silva Ribeiro ◽  
Ricardo Macedo Camelo ◽  
Josias Inácio da Silva ◽  
Moana Vergetti Malta ◽  
Rafael Costa Camelo ◽  
...  
Keyword(s):  
Case Report ◽  
Epidermoid Cyst ◽  
Fourth Ventricle ◽  
Slow Growth ◽  
Obstructive Hydrocephalus ◽  
Intracranial Tumors ◽  
Pathological Anatomy ◽  
Cerebellar Syndrome ◽  
The Third ◽  
The Ideal

AbstractEpidermoid cysts constitute congenital, benign and rare lesions, corresponding to ∼ 0.2% to 1.8% of all intracranial tumors. Only 5% of the cases are located in the fourth ventricle. Despite their genesis in intrauterine life, they are usually diagnosed between the third and fifth decades of life due to their very slow growth pattern. The image weighted by the diffusion of the magnetic resonance is essential to establish the diagnosis. The ideal treatment consists of emptying the cystic content with complete capsule resection. In the present work, we report the case of a 31-year-old female with cerebellar syndrome that evolved with intracranial hypertension. The symptomatology was due to an obstructive hydrocephalus by an epidermoid cyst located inside the fourth ventricle, which was confirmed by the pathological anatomy.

scholarly journals Cerebellar syndrome in calf: case report

2017 ◽  
Vol 15 (Suppl 2) ◽  
pp. 411
Author(s):  
José Victor Pronievicz Barreto et al.
Keyword(s):  
Case Report ◽  
Cerebellar Syndrome

scholarly journals Case Report on Phenytoin Induced Cerebellar Syndrome

2018 ◽  
Vol 11 (1) ◽  
pp. 58-60
Author(s):  
Gautam Satheesh ◽  
Sujith Varma K ◽  
Anil Antony
Keyword(s):  
Case Report ◽  
Cerebellar Syndrome

scholarly journals Cerebellar Syndrome Revealing a Giant Postero Inferior Cerebellar Artery Aneurysm: A Case Report and a Review of Literature

2021 ◽  
Vol 10 (06) ◽  
pp. 153-159
Author(s):  
Oumar Diallo ◽  
Maiga Abdoulaye Hima ◽  
Beketi Katanga Anthony ◽  
Thioub Mbaye ◽  
Mahamadou Dama ◽  
...  
Keyword(s):  
Case Report ◽  
Artery Aneurysm ◽  
Review Of Literature ◽  
Cerebellar Syndrome ◽  
Cerebellar Artery

scholarly journals Acute cerebellar syndrome after high dose cytosine arabinoside treatment: case report

2020 ◽  
Vol 42 ◽  
pp. 36
Author(s):  
F. Yilmaz ◽  
M. Tiglioglu ◽  
P. Akyol ◽  
M. Reis Aras ◽  
B. SagLam ◽  
...  
Keyword(s):  
Case Report ◽  
Cytosine Arabinoside ◽  
High Dose ◽  
Cerebellar Syndrome
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