Intracranial EEG Monitoring in Landau-Kleffner Syndrome Associated with Left Temporal Lobe Astrocytoma

Epilepsia ◽  
1993 ◽  
Vol 34 (3) ◽  
pp. 557-560 ◽  
Author(s):  
Gail E. Solomon ◽  
Deborah Carson ◽  
Steven Pavlakis ◽  
Richard Fraser ◽  
Douglas Labar
Neurology ◽  
2015 ◽  
Vol 85 (17) ◽  
pp. 1475-1481 ◽  
Author(s):  
Robyn M. Busch ◽  
Thomas E. Love ◽  
Lara E. Jehi ◽  
Lisa Ferguson ◽  
Ruta Yardi ◽  
...  

Neurosciences ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 261-269
Author(s):  
Abeer Khoja ◽  
Omnyah Albaradei ◽  
Ashwaq Alsulami ◽  
Mohamed Alkhaja ◽  
Mohammad Alsumaili ◽  
...  

2008 ◽  
Vol 39 (01) ◽  
Author(s):  
AN Datta ◽  
I Jambaqué ◽  
G Dellatolas ◽  
C Bulteau ◽  
M Fohlen ◽  
...  

Epilepsia ◽  
1996 ◽  
Vol 37 (7) ◽  
pp. 651-656 ◽  
Author(s):  
Gregory D. Cascino ◽  
Max R. Trenerry ◽  
Elson L. So ◽  
Frank W. Sharbrough ◽  
Cheolsu Shin ◽  
...  

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098281
Author(s):  
Liang Zhang ◽  
Hao Yu ◽  
Dan Li ◽  
Hui Qian ◽  
Yuchao Chen

Epilepsy is a chronic neurological disorder that is characterized by episodes of seizure. Sexual dysfunction has been reported in patients with seizure, which mostly manifests as erectile dysfunction and premature ejaculation in men. In this study, we report the case of a 65-year-old Chinese man with frequent spermatorrhea. Electroencephalography suggested local epilepsy in the left temporal lobe. After treatment with anti-epilepsy drugs, the symptoms disappeared and did not recur. To the best of our knowledge, this is the first reported case of epilepsy-induced spermatorrhea. The symptoms of spermatorrhea are probably a rare manifestation of seizure. When repetitive stereotyped symptoms occur, seizure should be considered, and tentative anti-epileptic treatment may be a good option.


2008 ◽  
Vol 46 (2) ◽  
pp. 455-460 ◽  
Author(s):  
W.C.J. Alpherts ◽  
J. Vermeulen ◽  
P.C. van Rijen ◽  
F.H. Lopes da Silva ◽  
C.W.M. van Veelen

2011 ◽  
Vol 21 (1) ◽  
pp. 94-99 ◽  
Author(s):  
Shigeki Sunaga ◽  
Michiharu Morino ◽  
Taro Kusakabe ◽  
Hidenori Sugano ◽  
Hiroyuki Shimizu

2006 ◽  
Vol 59 (2) ◽  
pp. 335-343 ◽  
Author(s):  
Anthony B. Waites ◽  
Regula S. Briellmann ◽  
Michael M. Saling ◽  
David F. Abbott ◽  
Graeme D. Jackson

1992 ◽  
Vol 50 (4) ◽  
pp. 539-542 ◽  
Author(s):  
Nélida S. Garretto ◽  
David Monteverde ◽  
Héctor Giócoli ◽  
Blanca I. Ravera ◽  
Hugo A. Molina ◽  
...  

Schwannomatosis is a rare disorder, still not quite well defined, seldom described in the literature. In this paper we report the case of male. Patient, 52 years old, who in the last 30 years developed five subcutaneous tumors within his limbs peripheral nerves, which histologically proved to be schwannomas. A brain computed tomography showed a partially calcified tumor in the left temporal lobe which most likely was a meningioma. A thorough clinical examination was unable to find signs of type I or type II neurofibromatosis. The present condition, probably a form of phacomatosis, has to be distinguished from neurofibromatosis and is considered as an independent clinical entity whose origin still awaits further detailed investigations.


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