Department of Neurosurgery, Rush University Medical Center, 1653 West Congress Pkwy, Chicago, IL 60612-3244
J Clin Psychiatry. 2013 Nov;74(11):1071-5. doi: 10.4088/JCP.13m08378.
Indolent low-grade temporal lobe tumors may present with ictal panic that may be difficult to differentiate from psychogenic panic attacks. The current study aims to demonstrate the differences between the two disorders and help physicians generate a diagnostic paradigm.
This was a retrospective study of 43 patients who underwent a temporal lobectomy between 1981 and 2008 for the treatment of intractable temporal lobe epilepsy secondary to low-grade neoplasms at Rush University Medical Center. A total of 10 patients in this group presented with ictal panic who were previously being treated for psychogenic panic attacks. Medical records were reviewed for age at seizure onset, duration of symptoms, lateralization of the epileptogenic zone, pathological diagnosis, and postsurgical seizure outcome according to the modified Engel classification.
Neuropathologic findings of the 10 tumors were pleomorphic xanthoastrocytoma, ganglioglioma, oligodendroglioma, and dysembryoplastic neuroepithelial. The mean age of the patients undergoing surgery was 28 years (range, 15-49). The mean duration of panic symptoms prior to surgery was 9.8 years (range, 3-23). All patients had unprovoked ictal panic. None had symptoms suggestive of a brain tumor, such as signs of increased intracranial pressure or any focal neurologic deficit. In 5 of the patients, other symptoms associated with the ictal panic, including unusual sounds, nausea, automatism, uprising gastric sensation, and déjà vu were identified. Gross total resection of the lesion resulted in improved seizure outcome in all patients undergoing surgery. Patient follow-up was, on average, 7.4 years (range, 2-14) from time of surgery.
Although similar, ictal panic from epilepsy and classic panic attacks are clinically distinguishable entities with different modalities of treatment. A careful history may help differentiate patients with ictal panic from those with psychogenic panic attacks and determine for which patients to obtain neuroimaging studies.
惰性低级别颞叶肿瘤可能表现为发作性惊恐,这可能难以与心因性惊恐发作相区分。本研究旨在展示两种疾病之间的差异,并帮助医生制定诊断模式。
这是一项回顾性研究,纳入了 1981 年至 2008 年期间在 Rush 大学医学中心因低级别肿瘤继发难治性颞叶癫痫而行颞叶切除术的 43 名患者。该组中有 10 名患者发作性惊恐,此前被诊断为心因性惊恐发作,正在接受治疗。回顾了患者的年龄、癫痫发作起始年龄、症状持续时间、致痫区的侧化、病理诊断以及根据改良的 Engel 分级的术后癫痫发作结局。
10 例肿瘤的神经病理学发现为多形性黄色星形细胞瘤、节细胞瘤、少突胶质细胞瘤和发育不良性神经上皮瘤。手术患者的平均年龄为 28 岁(15-49 岁)。手术前惊恐症状的平均持续时间为 9.8 年(3-23 年)。所有患者均有自发性发作性惊恐。无患者出现提示脑肿瘤的症状,如颅内压增高的迹象或任何局灶性神经功能缺损。在 5 例患者中,识别出了与发作性惊恐相关的其他症状,包括异常声音、恶心、自动症、上升胃感觉和即视感。病变的大体全切除导致所有手术患者的癫痫发作结局改善。患者平均随访时间为手术时起 7.4 年(2-14 年)。
尽管相似,癫痫发作性惊恐和典型惊恐发作是临床上可区分的实体,治疗方式也不同。仔细的病史可以帮助区分发作性惊恐患者和心因性惊恐发作患者,并确定哪些患者需要进行神经影像学检查。