Focal cortical dysplasia with calcification: a case report

2007 ◽  
Vol 24 (5) ◽  
pp. 619-622 ◽  
Author(s):  
Kazuhiro Samura ◽  
Takato Morioka ◽  
Fumiaki Yoshida ◽  
Kimiaki Hashiguchi ◽  
Yasushi Miyagi ◽  
...  
2020 ◽  
Vol 36 (7) ◽  
pp. 1557-1561 ◽  
Author(s):  
Lídia Nunes Dias ◽  
Santiago Candela-Cantó ◽  
Cristina Jou ◽  
Javier Aparicio Calvo ◽  
Sergio García-García ◽  
...  

2010 ◽  
Vol 31 (4) ◽  
pp. 433-439 ◽  
Author(s):  
Kenta Masui ◽  
Satoshi O. Suzuki ◽  
Kimiaki Hashiguchi ◽  
Takato Morioka ◽  
Takashi Yoshiura ◽  
...  

2014 ◽  
Vol 54 (7) ◽  
pp. 593-597 ◽  
Author(s):  
Noriaki MINAMI ◽  
Takehiro UDA ◽  
Takahiro MATSUMOTO ◽  
Taiki NAGAI ◽  
Tatsuya UCHIDA ◽  
...  

2009 ◽  
Vol 25 (11) ◽  
pp. 1501-1506 ◽  
Author(s):  
Kuo-Liang Chiang ◽  
Tai-Tong Wong ◽  
Shan-Young Kwan ◽  
Ting-Rong Hsu ◽  
Chung-Hao Wang ◽  
...  

1988 ◽  
Vol 12 (1) ◽  
pp. 61-63 ◽  
Author(s):  
Martha A. Nowell ◽  
Robert I. Grossman ◽  
Roger Packer ◽  
David B. Hackney ◽  
Herbert I. Goldberg ◽  
...  

2021 ◽  
Vol 11 (9) ◽  
pp. 1136
Author(s):  
Keisuke Hatano ◽  
Ayataka Fujimoto ◽  
Chikanori Inenaga ◽  
Yoshiro Otsuki ◽  
Hideo Enoki ◽  
...  

Background: Intracranial dermoid cyst is a rare, benign, nonneoplastic tumor-like lesion that could cause seizures, headache, and hydrocephalus. We hypothesized that the temporal lobe dermoid cyst in combination with other factors were causing the epileptic seizure. Methods: We encountered a 17-year-old girl with anti-seizure medication-resistant epilepsy secondary to dermoid cyst located in the temporal region depicted on magnetic resonance imaging (MRI). She showed neither symptoms of meningitis nor rupture of the cyst according to serial MRI. We hypothesized that temporal lobe dermoid cyst in combination with other factors, such as focal cortical dysplasia (FCD), etc., was causing epileptic seizures in this case. She underwent dermoid cyst removal surgery with resection of the tip of the antero-inferior temporal lobe. Results: Histopathological study showed multiple small intramedullary dermoid cysts in the left antero-inferior temporal lobe in addition to MRI lesions and FCD. Conclusion: A patient with medically intractable epilepsy secondary to left temporal lobe dermoid cyst showed multiple intramedullary dermoid cysts and focal cortical dysplasia that might have interacted to create epileptogenicity. To our knowledge, this is the first case report of dermoid cyst concomitant with FCD.


2011 ◽  
Vol 33 (8) ◽  
pp. 683-686 ◽  
Author(s):  
Sara Marconi ◽  
Gaetano Cantalupo ◽  
Federica Marliani ◽  
Francesco Toni ◽  
Giuseppe Capovilla ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Antonio G. Nicotera ◽  
Maria Spanò ◽  
Alice Decio ◽  
Giulia Valentini ◽  
Maria Saia ◽  
...  

Epilepsy is a rare clinical manifestation in Williams–Beuren syndrome patients. However, some studies report the presence of infantile spasms and epilepsy in patients carrying larger deletions. Herein, we describe a 13-year-old female affected by Williams–Beuren syndrome and pharmacoresistant epilepsy reporting a de novo large heterozygous 7q11.21q21 deletion (19.4 Mb) also including the YWHAG gene. Studies indicate that cannabidiol is effective as adjunctive therapy for seizures associated with tuberous sclerosis complex, and it is under investigation also in focal cortical dysplasia. When treated with cannabidiol, our patient showed a significant reduction in seizure frequency and intensity, and improved motor and social skills. We hypothesized that CBD could exert a gene/disease-specific effect.


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