成人肝移植受者巨细胞病毒相关格林-巴利综合征1例报告

Q3 Medicine
Infectio Pub Date : 2023-09-06 DOI:10.22354/24223794.1144
Diana Marcela Hoyos-Llanos, Nicolas Andres Cortes-Mejia, Daniela Lucia Rico-Bolivar, Paula Giraldo-Posada, Francisco Alexander Perez-Rengifo, Alonso Vera-Torres
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引用次数: 0

摘要

吉兰-巴罗综合征(GBS)是一种免疫介导的疾病,影响运动和感觉脊髓根和周围神经。GBS是一种罕见的疾病,其全球发病率低至每10万人每年0.81至1.89例。尽管其发病率低,但GBS具有重要的发病率和致命潜力。这种综合征通常是由感染引起的。由于其临床表现的异质性和疾病的自然史,对于该实体的管理,缺乏国际临床实践指南。在本报告中,我们报告了一位67岁的男性患者,在肝移植(LT)后的第五个月,他出现了急性非炎症性腹泻,随后出现突然上升对称性麻痹和脚底感觉异常。电生理学研究报告脱髓鞘炎性多根神经病变与GBS相容,急性严重炎性脱髓鞘性多神经病变(AIDP)亚型。他的神经功能缺陷与同时原发性巨细胞病毒(CMV)感染有关,巨细胞病毒是最常见的与gbs相关的感染因子之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytomegalovirus-related Guillain-Barre syndrome in an adult liver transplant recipient: a case report
Guillain-Barré syndrome (GBS) is an immune-mediated condition affecting both the motor and sensory spinal roots and peripheric nerves. GBS is a rare entity, with its global incidence being as low as 0.81 to 1.89 cases per 100.000 person-year. Despite its low incidence, GBS have an important morbidity and lethal potential. This syndrome is usually triggered by infections. Due to its clinical presentation heterogeneity and its disease natural history, there is scarse availability of international clinical practice guidelines for the management of this entity. In this report, we present the case of a 67 years-old man on his fifth month after liver transplant (LT), who developed acute non-inflammatory diarrhea followed by sudden ascending symmetric paresia and soles paresthesias. Electrophysiologic studies reported a demyelinating inflammatory polyradiculoneuropathy compatible with GBS, acute severe inflammatory demyelinating polyneuropathy (AIDP) subtype. His neurolo¬gy deficit was associated with a simultaneous primary Cytomegalovirus (CMV) infection, one of the most common GBS-related infectious agents.
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来源期刊
Infectio
Infectio Medicine-Pharmacology (medical)
CiteScore
1.50
自引率
0.00%
发文量
18
审稿时长
39 weeks
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