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帕金森病运动不能危象并发重症疾病性神经肌肉病:3例报告

Critical Illness Neuromyopathy Complicating Akinetic Crisis in Parkinsonism: Report of 3 Cases.

作者信息

Capasso Margherita, De Angelis Maria Vittoria, Di Muzio Antonio, Anzellotti Francesca, Bonanni Laura, Thomas Astrid, Onofrj Marco

机构信息

From the Neurology Clinic (MC, MVD, AD, FA, LB, MO), "SS Annunziata" Hospital; and Department of Neuroscience and Imaging (LB, AT, MO), University "G. d'Annunzio" of Chieti-Pescara, Chieti, Italy.

出版信息

Medicine (Baltimore). 2015 Jul;94(28):e1118. doi: 10.1097/MD.0000000000001118.

Abstract

Akinetic crisis (AC) is a life-threatening complication of parkinsonism characterized by an acute severe akinetic-hypertonic state, consciousness disturbance, hyperthermia, and muscle enzymes elevation. Injectable dopaminomimetic drugs, high-dose methylprednisolone, and dantrolene are advocated as putative specific treatments. The course of the illness is frequently complicated by infections, pulmonary embolism, renal failure, disseminated intravascular coagulation, and cardiac arrhythmias. Critical illness neuromyopathy (CINM) is an acquired neuromuscular disorder characterized by flaccid quadriparesis and muscle enzyme elevation, often occurring in intensive care units and primarily associated with inactivity, sepsis, multiorgan failure, neuromuscular blocking agents, and steroid treatment. In 3 parkinsonian patients, during the course of AC we observed disappearance of rigidity but persistent hypoactivity. In all, neurological examination showed quadriparesis with loss of tendon reflexes and laboratory investigation disclosed a second peak of muscle enzymes elevation, following the first increment due to AC. Electrophysiological studies showed absent or reduced sensory nerve action potentials and compound muscular action potentials, myopathic changes, and fibrillation potentials at electromyography recordings, and reduced excitability or inexcitability of tibialis anterior at direct muscle stimulation, leading to a diagnosis of CINM in all 3 patients. In 1 patient, the diagnosis was also confirmed by muscle biopsy. Outcome was fatal in 2 of the 3 patients. Although AC is associated with most of the known risk factors for CINM, the cooccurrence of the 2 disorders may be difficult to recognize and has never been reported. We found that CINM can occur as a severe complication of AC, and should be suspected when hypertonia-rigidity subsides despite persistent akinesia. Strict monitoring of muscle enzyme levels may help diagnosis. This finding addresses possible caveats in the use of putative treatments for AC.

摘要

运动不能危象(AC)是帕金森病的一种危及生命的并发症,其特征为急性严重运动不能-高张状态、意识障碍、高热及肌肉酶升高。注射用拟多巴胺药物、大剂量甲基强的松龙及丹曲林被推荐为可能的特异性治疗方法。该病病程常并发感染、肺栓塞、肾衰竭、弥散性血管内凝血及心律失常。危重病性神经肌肉病(CINM)是一种获得性神经肌肉疾病,其特征为弛缓性四肢瘫及肌肉酶升高,常发生于重症监护病房,主要与活动减少、脓毒症、多器官功能衰竭、神经肌肉阻滞剂及类固醇治疗有关。在3例帕金森病患者中,在AC病程中我们观察到强直消失但活动减少持续存在。总体而言,神经系统检查显示四肢瘫且腱反射消失,实验室检查发现,继AC导致的首次升高之后,肌肉酶升高出现第二个峰值。电生理研究显示感觉神经动作电位及复合肌肉动作电位缺失或降低、肌电图记录出现肌病性改变及纤颤电位,直接肌肉刺激时胫前肌兴奋性降低或无兴奋性,这3例患者均诊断为CINM。1例患者的诊断也通过肌肉活检得以证实。3例患者中有2例预后不良。尽管AC与CINM的大多数已知危险因素相关,但这两种疾病的同时发生可能难以识别,且此前从未有过报道。我们发现CINM可作为AC的一种严重并发症出现,当尽管运动不能持续存在但张力亢进-强直消退时应怀疑该病。严格监测肌肉酶水平可能有助于诊断。这一发现提示了AC假定治疗方法使用中可能存在的注意事项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01d4/4617089/455f2e720b4a/medi-94-e1118-g001.jpg

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