Case of Acute Inflammatory Demyelinating Polyneuropathy in SARS COVID 19 Pneumonia

V. T. Gonuguntla, A. Bernstein, Y. Kupfer
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Abstract

Introduction: Severe acute respiratory syndrome from COVID 19 typically presents with cough, fever, myalgias and progresses to respiratory and multi-organ failure. However, neurological manifestations of COVID 19, namely Guillain-Barre syndrome are rare. We present a case of acute inflammatory demyelinating polyneuropathy (AIDP), a form of GBS in a patient with recent COVID infection. Case: 66 year old man with no significant medical history presented to the emergency department for progressive weakness of all extremities for 2 days. Patient was diagnosed with COVID 19 three weeks prior to onset of weakness. As per patient, he only had mild respiratory illness with cough, general weakness without respiratory symptoms. Two days prior to presentation, he felt weakness in his lower extremities, which then progressed to involve the upper extremities. On initial evaluation the patient's pupils were symmetric and 3mm, reactive to light, visual field were full to confrontation, cranial nerves intact, shoulder shrug symmetric with full strength. He had decreased motor tone with 2/5 strength in both upper and lower extremities and depressed or absent reflexes in all extremities. His labs were significant for positive COVID 19 PCR and antibodies. CT head was negative for acute stroke or intracranial pathology. The patient was admitted to MICU where he developed respiratory muscle weakness with diminished vital capacity of 12ml/kg and negative inspiratory force of 12mmHg and he was intubated. Cerebral spinal fluid showed elevated protein to 145mg/dL, WBC of 4/UL with 50% lymphocytes and glucose of 67. Other CSF studies were negative for oligoclonal bands, EBV, CMV, cryptococcus, syphilis, and sarcoidosis. Electromyography was consistent with moderate AIDP. He received 5 doses of IVIG with no significant improvement so he underwent tracheostomy and was initiated on plasmapheresis for AIDP. Discussion: GBS is an immune-mediated disease that typically affects the peripheral neurons and nerve roots after respiratory or gastrointestinal illness. Typical infections are Campylobacter jejuni, Zika virus, Influenza, and there are even reports of GBS after MERS and SARS COV-1. However, there has been increasing evidence of COVID 19 causing neurologic manifestations such as encephalitis, meningitis, stroke, and GBS [1]. Patients, such as the one presented in this report with GBS, usually have a long and protracted disease despite aggressive treatments with IVIG and plasmapheresis with reliance on mechanical ventilator. Understanding the full spectrum of diseases and systems affected by COVID 19 can help clinicians provide better care.
SARS - COVID - 19肺炎急性炎性脱髓鞘性多神经病变1例
COVID - 19引起的严重急性呼吸综合征通常表现为咳嗽、发烧、肌痛,并发展为呼吸和多器官衰竭。然而,COVID - 19的神经系统表现,即格林-巴利综合征是罕见的。我们提出一例急性炎症性脱髓鞘多神经病变(AIDP),一种形式的GBS在患者最近的COVID感染。病例:66岁男性,无明显病史,因进行性四肢无力2天到急诊科就诊。患者在开始虚弱前三周被诊断出患有COVID - 19。根据病人的资料,他只有轻微的呼吸道疾病,包括咳嗽和全身无力,没有呼吸道症状。就诊前两天,患者感到下肢无力,随后发展至上肢。初步评估患者瞳孔对称3mm,对光有反应,视野完全对视,颅神经完整,肩胛对称,力量充分。患者上肢和下肢运动张力下降,强度为2/5,四肢反射抑制或缺失。他的实验室检测结果为COVID - 19 PCR阳性和抗体阳性。CT头部未见急性脑卒中或颅内病理。患者入住MICU,出现呼吸肌无力,肺活量下降12ml/kg,吸气力负12mmHg,插管。脑脊液蛋白升高至145mg/dL,白细胞4/UL,淋巴细胞50%,葡萄糖67。其他脑脊液研究对寡克隆带、EBV、CMV、隐球菌、梅毒和结节病均呈阴性。肌电图与中度AIDP一致。他接受了5剂IVIG治疗,但没有明显改善,因此他接受了气管切开术,并开始进行血浆置换治疗AIDP。讨论:GBS是一种免疫介导的疾病,通常在呼吸或胃肠道疾病后影响周围神经元和神经根。典型的感染是空肠弯曲杆菌、寨卡病毒、流感,甚至在MERS和SARS - COV-1之后也有GBS的报道。然而,越来越多的证据表明,COVID - 19可引起脑炎、脑膜炎、中风和GBS等神经系统表现[1]。尽管采用IVIG和血浆置换等积极治疗并依赖机械呼吸机,但GBS患者(如本报告中出现的患者)的病程通常较长且持续时间较长。全面了解受COVID - 19影响的疾病和系统可以帮助临床医生提供更好的护理。
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