Alkawadri Rafeed, Mickey Bruce E, Madden Christopher J, Van Ness Paul C
Epilepsy Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Arch Neurol. 2011 Mar;68(3):381-5. doi: 10.1001/archneurol.2011.21.
Cingulate gyrus epilepsy is controversial because it may overlap with other frontal lobe epilepsy syndromes. Reported cases are rare in the pre-magnetic resonance imaging literature but are more common thereafter. Information about peri-ictal and ictal behaviors is scarce.
To characterize epilepsy originating from the cingulate gyrus and to report surgical outcomes.
Case studies.
Academic research.
We report 3 surgically treated cases of cingulate gyrus epilepsy, with seizure-free or almost seizure-free outcomes. The cases were identified from a database of 4201 consecutive epilepsy monitoring unit admissions since October 1998 through September 2008. All 3 cases involved cingulate lesions.
Neuroimaging, video electroencephalographic, pathologic, and surgical outcome data were reviewed.
All 3 patients had lesional left anterocingulate seizures confirmed by magnetic resonance imaging and experienced cessation of seizures after lesionectomy. Two patients had auras (fear and laughter) previously associated with cingulate gyrus epilepsy. All patients had clinical features consistent with frontal lobe epilepsy, including hyperkinetic behavior and ictal vocalization. Two patients had behavioral changes with aggression, personality disorder, and poor judgment; some behavioral episodes lasted for days and were socially devastating. One patient, a commercial pilot, showed behavior as a passenger that resulted in a diversionary landing. The other patient demonstrated behavior that led to his arrest, and he was almost arrested again in the hospital for threatening security officers. Aberrant behaviors in all 3 patients completely resolved after lesionectomy.
Lesional cingulate gyrus epilepsy is uncommon. Our 3 confirmed cases included 2 patients with unique and severe behavioral changes that resolved with lesionectomy.
扣带回癫痫存在争议,因为它可能与其他额叶癫痫综合征重叠。在磁共振成像出现之前的文献中,报道的病例很少,但此后较为常见。关于发作期和发作间期行为的信息很少。
描述起源于扣带回的癫痫并报告手术结果。
病例研究。
学术研究。
我们报告3例接受手术治疗的扣带回癫痫病例,术后无发作或几乎无发作。这些病例是从1998年10月至2008年9月连续4201例癫痫监测单元入院病例的数据库中识别出来的。所有3例均涉及扣带回病变。
回顾神经影像学、视频脑电图、病理学和手术结果数据。
所有3例患者经磁共振成像证实为左侧前扣带回病灶性癫痫,病灶切除术后癫痫发作停止。2例患者有先前与扣带回癫痫相关的先兆(恐惧和大笑)。所有患者的临床特征均与额叶癫痫一致,包括运动过多行为和发作期发声。2例患者有攻击性行为、人格障碍和判断力差等行为改变;一些行为发作持续数天,对社会造成严重破坏。1例患者是商业飞行员,作为乘客时出现行为异常导致改道降落。另1例患者的行为导致其被捕,在医院里他因威胁保安人员差点再次被捕。所有3例患者的异常行为在病灶切除术后完全消失。
病灶性扣带回癫痫并不常见。我们的3例确诊病例中有2例患者有独特且严重的行为改变,病灶切除术后这些改变消失。