Abidoye Oluseyi, Raybon-Rojas Erine, Ogbuagu Henry
Internal Medicine, Northeast Georgia Medical Center Gainesville, Gainesville, USA.
Critical Care Medicine, Northeast Georgia Medical Center Gainesville, Gainesville, USA.
Cureus. 2022 Jan 10;14(1):e21085. doi: 10.7759/cureus.21085. eCollection 2022 Jan.
Infectious mononucleosis (IM) is an acute disease caused by Epstein-Barr virus (EBV) infection affecting adolescents and young adults. Clinically, IM presents with fever, lymphadenopathy, and tonsillar pharyngitis. Guillain-Barré syndrome (GBS) has been reported as a possible rare complication of IM. IM-induced GBS is known but rarely reported in the literature. Here, we describe the case of a 19-year-old male with no significant medical history who was diagnosed with GBS following EBV-associated IM. A 19-year-old Caucasian male presented from a referring facility after complaining of generalized weakness involving the upper and lower extremity for about five days. Symptoms began with a sensation of tingling and numbness in the fingertips and toes that progressed over five days to where he was no longer able to ambulate. Physical examination was significant for oropharyngeal exudates, posterior oropharyngeal erythema, tonsillar hypertrophy, cervical lymphadenopathy, flaccid paralysis with areflexia, and paresthesia. Diagnostic workup was consistent with IM and GBS based on cerebrospinal findings. He was subsequently admitted to the intensive care unit, where he received plasmapheresis and intravenous immunoglobulin with significant improvement. This is a rare case of EBV-associated IM GBS. IM is a self-limiting disease but can lead to GBS as one of the known but rare complications. Neurological events have been reported in approximately 2% of patients. Only a few cases of IM leading to GBS have been reported in the literature. Detailed history and physical examination can help identify patients with IM-induced GBS. Moreover, increased awareness can help physicians easily identify and manage GBS, enabling timely recognition and initiation of prompt supportive care to improve recovery time.
传染性单核细胞增多症(IM)是由爱泼斯坦-巴尔病毒(EBV)感染引起的一种急性疾病,主要影响青少年和青年。临床上,IM表现为发热、淋巴结病和扁桃体咽炎。格林-巴利综合征(GBS)已被报道为IM可能的罕见并发症。IM诱发的GBS虽已为人所知,但在文献中很少报道。在此,我们描述了一例19岁男性患者,他没有明显的病史,在发生与EBV相关的IM后被诊断为GBS。一名19岁的白种男性患者从转诊机构前来就诊,他主诉上下肢广泛性无力约五天。症状始于指尖和脚趾的刺痛和麻木感,五天内逐渐发展到无法行走。体格检查发现口咽渗出物、口咽后部红斑、扁桃体肥大、颈部淋巴结病、弛缓性麻痹伴反射消失和感觉异常。根据脑脊液检查结果,诊断检查结果与IM和GBS相符。随后他被收入重症监护病房,在那里接受了血浆置换和静脉注射免疫球蛋白治疗,病情有显著改善。这是一例罕见的与EBV相关的IM合并GBS病例。IM是一种自限性疾病,但可导致GBS作为已知但罕见的并发症之一。据报道,约2%的患者会出现神经系统事件。文献中仅报道了少数几例IM导致GBS的病例。详细的病史和体格检查有助于识别IM诱发GBS的患者。此外,提高认识有助于医生轻松识别和管理GBS,从而能够及时识别并启动及时的支持性护理,以缩短恢复时间。