Purpose: Focal cortical dysplasia (FCD) is the most common pathological diagnosis in patients who have undergone surgical treatment for intractable neocortical epilepsy. However, presurgical identification of MRI abnormalities in FCD patients remains difficult, and there are no highly sensitive imaging parameters available that can reliably differentiate among FCD subtypes. The purpose of our study was to investigate the surgical outcome in FCD patients with identifiable MRI abnormalities and to evaluate the prognostic role of the various MRI features and the characteristics of FCD pathology. Methods: We retrospectively recruited epilepsy patients who had undergone surgical treatment for refractory epilepsy with focal MRI abnormalities and the pathological diagnosis of FCD. We evaluated the surgical outcome according to the pathological subtypes, and studied the prognostic roles of various MRI features. We used recently proposed three-tiered FCD classification system which included FCD type III when FCD occurs in association with other potentially epileptogenic pathologies. Results: A total of 69 patients were included, and 68.1% of patients became seizure free. Patients with FCD type III had a lower chance for achieving seizure freedom (7/15) than in patients with isolated FCD (FCD types I and 11)(40/54, p = 0.044). Cortical thickness and blurring of gray-white matter junction were more common in isolated FCD than in FCD type III, but most MRI features failed to differentiate between FCD types I and II, and only the transmantle sign was specific for FCD type II. We failed to find a prognostic value of specific MRI abnormalities of prognostic value in terms of post-epilepsy surgery outcome in FCD patients. Conclusions: Our study showed that patients with FCD III have poor surgical outcome. Typical MRI features of isolated FCD such as cortical thickness and blurring of gray-white matter junction were less common in FCD type HI and only transmantle sign was helpful in differentiating between FCD types I and II. (C) 2012 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
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Catholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
Kwon, Hye Eun
Eom, Soyong
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Yonsei Univ, Coll Med, Epilepsy Res Inst, Severance Childrens Hosp,Dept Pediat, Seoul, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
Eom, Soyong
Kang, Hoon-Chul
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Yonsei Univ, Coll Med, Div Pediat Neurol, Seoul, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
Kang, Hoon-Chul
Lee, Joon Soo
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Yonsei Univ, Coll Med, Div Pediat Neurol, Seoul, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
Lee, Joon Soo
Kim, Se Hoon
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Yonsei Univ, Coll Med, Severance Hosp, Dept Pathol, Seoul, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
Kim, Se Hoon
Kim, Dong Seok
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Yonsei Univ, Coll Med, Div Pediat Neurosurg, Seoul, South KoreaCatholic Kwandong Univ, Coll Med, Int St Marys Hosp, Dept Pediat, Inchon, South Korea
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Capital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R ChinaCapital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R China
Xue, Hai
Cai, Lixin
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Capital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R China
Peking Univ, Hosp 1, Pediat Epilepsy Ctr, Beijing 100034, Peoples R ChinaCapital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R China
Cai, Lixin
Dong, Sheng
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Capital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R ChinaCapital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R China
Dong, Sheng
Li, Yongjie
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Capital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R ChinaCapital Med Univ, Xuanwu Hosp, Dept Funct Neurosurg, Beijing 100069, Peoples R China
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Univ Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Choi, H. W.
Yum, M. S.
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Univ Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Yum, M. S.
Kim, E. H.
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Univ Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Kim, E. H.
Kim, S. A.
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Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Kim, S. A.
Kim, J. J.
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Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Kim, J. J.
Khang, S. K.
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Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Khang, S. K.
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Hong, S.
Lee, J. K.
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Univ Ulsan, Dept Neurosurg, Asan Med Ctr, Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea
Lee, J. K.
Ko, T. S.
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Univ Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South KoreaUniv Ulsan, Div Pediat Neurol, Dept Pediat, Asan Med Ctr,Childrens Hosp,Coll Med, Seoul, South Korea