Department of Neurosciences, Neurological Clinic, University of Pisa, via Roma 67, 56126, Pisa, Italy.
Neurol Sci. 2010 Jun;31(3):349-52. doi: 10.1007/s10072-009-0207-7. Epub 2010 Jan 30.
We report the case of a 32-year-old woman with a history of increased sleep need and difficulty waking up; the diagnosis of idiopathic hypersomnia was hypothesized. During ambulatory polysomnography (PSG), the patient presented an episode characterized by loss of consciousness and jerking of the four limbs. A video-PSG monitoring was performed and the patient showed unresponsiveness and drowsiness at 7 a.m. During the episode, EEG showed theta-delta diffuse activity, and blood glucose level was 32 mg dl(-1). The diagnosis of insulinoma was then assumed; CT scan showed a hypodense mass into the pancreatic tail, and a partial pancreasectomy was performed. The described symptoms disappeared, and 5 years later the findings of a complete clinical and neurophysiological examination were negative. The clinical picture of insulinoma presenting with paroxysmal disorders has been previously described; however, whereas hypersomnia is uncommon, in the current case it represents the main symptom. Clinicians should keep in mind that neuroglycopenia should be considered in the differential diagnosis of patients with hypersomnia, particularly if the clinical scenario does not conform to standard criteria.
我们报告了一例 32 岁女性患者,其病史为睡眠需求增加和难以醒来;假设为特发性嗜睡症。在门诊多导睡眠图(PSG)期间,患者出现了以意识丧失和四肢抽搐为特征的发作。进行了视频 PSG 监测,患者在上午 7 点表现出无反应和困倦。在发作期间,脑电图显示θ-δ弥漫性活动,血糖水平为 32 毫克/分升(mg/dl)。然后假设为胰岛素瘤的诊断;CT 扫描显示胰尾有一个低密病灶,并进行了部分胰腺切除术。描述的症状消失了,5 年后完全临床和神经生理学检查结果为阴性。胰岛素瘤表现为阵发性疾病的临床表现以前已有描述;然而,虽然嗜睡症并不常见,但在本例中它是主要症状。临床医生应记住,在嗜睡症患者的鉴别诊断中应考虑神经低血糖症,特别是如果临床情况不符合标准标准。