Wasey Waiz, Carter Caitlin, Badesha Nav S, Rossi Maria, Baig Malika
Family and Community Medicine, Southern Illinois University School of Medicine, Springfield, USA.
Psychiatry, Southern Illinois University School of Medicine, Springfield, USA.
Cureus. 2022 Apr 7;14(4):e23914. doi: 10.7759/cureus.23914. eCollection 2022 Apr.
Lance-Adams syndrome (LAS) is a rare complication of successful cardiopulmonary resuscitation, often accompanied by action myoclonus. Myoclonus may occur as generalized, focal, or multifocal movements and can include the face, trunk, and/or extremities. Only 100 cases of LAS have been reported worldwide. Here, we present the case of a 53-year-old female who had a cardiac arrest event after being admitted for posterior cervical wound dehiscence management following a posterior cervical fusion from C3-T1. The patient was successfully resuscitated but developed action myoclonus in all extremities shortly after. Anoxic brain injury and myoclonus led to debilitation and prolonged hospital stay. During her inpatient stay, she was treated with clonazepam, levetiracetam, and sodium valproate with mild improvement.
兰斯-亚当斯综合征(LAS)是心肺复苏成功后的一种罕见并发症,常伴有动作性肌阵挛。肌阵挛可表现为全身性、局灶性或多灶性运动,可累及面部、躯干和/或四肢。全球仅报道了100例LAS病例。在此,我们报告一例53岁女性病例,该患者在C3-T1后路颈椎融合术后因后路颈部伤口裂开入院治疗时发生心脏骤停事件。患者成功复苏,但随后不久四肢出现动作性肌阵挛。缺氧性脑损伤和肌阵挛导致身体虚弱和住院时间延长。在住院期间,她接受了氯硝西泮、左乙拉西坦和丙戊酸钠治疗,症状稍有改善。