Pillen Sigrid, Pizza Fabio, Dhondt Karlien, Scammell Thomas E, Overeem Sebastiaan
Sleep Medicine Center Kempenhaeghe, P.O. Box 61, , 5590 AB, Heeze, The Netherlands.
Department of Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Curr Treat Options Neurol. 2017 Jun;19(6):23. doi: 10.1007/s11940-017-0459-0.
This review describes the diagnosis and management of cataplexy: attacks of bilateral loss of muscle tone, triggered by emotions and with preserved consciousness. Although cataplexy is rare, its recognition is important as in most cases, it leads to a diagnosis of narcolepsy, a disorder that still takes a median of 9 years to be diagnosed. The expression of cataplexy varies widely, from partial episodes affecting only the neck muscles to generalized attacks leading to falls. Moreover, childhood cataplexy differs from the presentation in adults, with a prominent facial involvement, already evident without clear emotional triggers ('cataplectic facies') and 'active' motor phenomena especially of the tongue and perioral muscles. Next to narcolepsy, cataplexy can sometimes be caused by other diseases, such as Niemann-Pick type C, Prader Willi Syndrome, or lesions in the hypothalamic or pontomedullary region. Cataplexy mimics include syncope, epilepsy, hyperekplexia, drop attacks and pseudocataplexy. They can be differentiated from cataplexy using thorough history taking, supplemented with (home)video recordings whenever possible. Childhood narcolepsy, with its profound facial hypotonia, can be confused with neuromuscular disorders, and the active motor phenomenona resemble those found in childhood movement disorders such as Sydenham's chorea. Currently, the diagnosis of cataplexy is made almost solely on clinical grounds, based on history taking and (home) videos. Cataplexy shows remarkable differences in childhood compared to adults, with profound facial hypotonia and complex active motor phenomena. Over time, these severe symptoms evolve to the milder adult phenotype, and this pattern is crucial to recognize when assessing the outcome of uncontrolled case series with potential treatments such as immunomodulation. Symptomatic treatment is possible with antidepressants and sodium oxybate. Importantly, management also needs to involve sleep hygiene advice, safety measures whenever applicable and guidance with regard to the social sequelae of cataplexy.
由情绪引发且意识清醒的双侧肌张力丧失发作。尽管猝倒症罕见,但识别它很重要,因为在大多数情况下,它会导致发作性睡病的诊断,而这种疾病的诊断中位时间仍为9年。猝倒症的表现差异很大,从仅影响颈部肌肉的部分发作到导致跌倒的全身性发作。此外,儿童猝倒症与成人表现不同,面部受累明显,在无明确情绪触发因素时就已明显(“猝倒面容”),还有“活跃”的运动现象,尤其是舌头和口周肌肉的运动现象。除发作性睡病外,猝倒症有时还可由其他疾病引起,如尼曼-匹克C型病、普拉德-威利综合征,或下丘脑或脑桥延髓区域的病变。猝倒症的模仿疾病包括晕厥、癫痫、僵人综合征、跌倒发作和假性猝倒症。通过详细的病史采集,并尽可能辅以(家庭)录像,可以将它们与猝倒症区分开来。儿童发作性睡病伴有严重的面部肌张力减退,可能会与神经肌肉疾病混淆,其活跃的运动现象类似于儿童运动障碍,如 Sydenham 舞蹈病。目前,猝倒症几乎完全基于临床依据进行诊断,依据病史采集和(家庭)录像。与成人相比,儿童猝倒症有显著差异,表现为严重的面部肌张力减退和复杂的活跃运动现象。随着时间推移,这些严重症状会演变为较轻的成人表型,在评估免疫调节等潜在治疗方法对未控制病例系列的疗效时,识别这种模式至关重要。使用抗抑郁药和羟丁酸钠可以进行对症治疗。重要的是,管理还需要包括睡眠卫生建议、适用时的安全措施以及关于猝倒症社会后遗症的指导。