scholarly journals Acute Onset Focal Epilepsy Mimicking Stroke

Cureus ◽  
2021 ◽  
Author(s):  
Marilena Mangiardi ◽  
Sabrina Anticoli ◽  
Luca Bertaccini ◽  
Valeria Cozzolino ◽  
Francesca Romana Pezzella
Keyword(s):  
1994 ◽  
Vol 8 (1) ◽  
pp. 45-48
Author(s):  
Anne G Sheehan ◽  
Sherry Pelensky ◽  
Colin Van Orman ◽  
Steven R Martin

Gastroesophageal reflux has been associated with, and implicated in, a number of conditions, including respiratory disease (recurrent pneumonia, chronic cough, asthma), sudden infant death syndrome, dysphagia and central nervous disorders. An eight-year-old girl presented with an acute history that suggested gastroesophageal reflux. An esophageal motility study was abnormal and 24 h pH study demonstrated gastroesophageal reflux. Before the manometric study, a seizure was observed and subsequent neurological evaluation confirmed the diagnosis of benign focal epilepsy of childhood, which was treated with carbamazepine. The symptoms resolved after eight weeks and the repeat reflux investigations were essentially normal. Oropharyngeal symptoms are common in benign focal epilepsy of childhood, a condition which is very responsive to therapy. Symptoms suggestive of this diagnosis - acute onset, with unusual oropharyngeal sensations, or seizures-occurring mainly at night may initially be confused with gastroesophageal reflux. Benign focal epilepsy of childhood should be considered in reflux presenting outside infancy.


2020 ◽  
Vol 13 (2) ◽  
pp. e233397
Author(s):  
Madhuri Laxman Khilari ◽  
Praveen Kumar Sharma

A 7-year-old child who suffered from symptomatic focal epilepsy as a sequel to perinatal hypoxia used to have frequent seizures. This time she developed prolonged status epilepticus lasting for over 5 hours. She received a treatment in the form of intravenous midazolam and reinitiation of sodium valproate and clobazam that were discontinued previously. Seizures were controlled over a couple of hours, but she remained unresponsive. Later, she developed acute onset dystonia (day 3 post-status epilepticus) and also myoclonic jerks. She presented to us after 3 weeks of onset of these complaints and we considered hypoxic encephalopathy resulting from prolonged status epilepticus or acute encephalitis or non-convulsive status epilepticus. However, acute onset dystonia and periodicity of myoclonic jerks were pointers against it, and on evaluation, she was diagnosed with atypical fulminant subacute sclerosing panencephalitis (SSPE). Knowing the atypical presentations of SSPE is important in planning management and prognostication.


2021 ◽  
Vol 14 (6) ◽  
pp. e242953
Author(s):  
Kunle Oyedokun ◽  
Maha ME Agabna ◽  
Anil Israni ◽  
Daniel du Plessis

A 3-year-old boy presented with acute onset of prolonged right sided focal seizures with secondary generalisation. The investigation findings were suggestive of a neoplastic process more than an inflammatory process. Decision to perform brain biopsy from the lesion to establish the precise nature of lesion was undertaken.


2011 ◽  
Vol 42 (S 01) ◽  
Author(s):  
T Getzinger ◽  
T Pieper ◽  
S Keßler-Uberti ◽  
B Pascher ◽  
H Eitel ◽  
...  

2017 ◽  
Vol 48 (S 01) ◽  
pp. S1-S45
Author(s):  
A. Herting ◽  
T. Cloppenborg ◽  
A. Hofmann-Peters ◽  
T. Polster

2018 ◽  
Author(s):  
Kristina Ungerath ◽  
Grischa Lischetzki ◽  
Birgit Schipper ◽  
Stefanie Beck-Wödl
Keyword(s):  

2008 ◽  
Vol 39 (01) ◽  
Author(s):  
A Peraud ◽  
F Heinen ◽  
S Noachtar ◽  
J Ilmberger ◽  
PA Winkler ◽  
...  
Keyword(s):  

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