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以吉兰-巴雷综合征自主神经功能障碍为表现的应激性心肌病:病例系列及文献综述

Takotsubo Cardiomyopathy as a Manifestation of Dysautonomia in Guillain-Barré Syndrome: A Case Series and Review of the Literature.

作者信息

Puentes Dyanet, Teijelo Daniela, Stiep Tamara S, Mannava Sishir, Margolesky Jason

机构信息

Neurology, University of Miami, Miami, USA.

出版信息

Cureus. 2021 Jun 30;13(6):e16069. doi: 10.7759/cureus.16069. eCollection 2021 Jun.

Abstract

Guillain-Barré syndrome (GBS) is an inflammatory polyneuropathy that classically presents with low back pain, sensory paresthesias, and rapidly progressive weakness. Patients with GBS can develop dysautonomia, and Takotsubo cardiomyopathy (TCM) is a rare potential manifestation of this dysautonomia. This association has been reported only 12 times in the literature so far, which we review here. We present two cases of GBS associated with TCM, to increase awareness with regard to this comorbid relationship, which would encourage prompt initiation of proper supportive care to avoid morbidity and mortality. We report the case of two patients - a 58-year-old man and a 79-year-old woman - who developed TCM in the setting of axonal variants of GBS. Electrodiagnostic results, cerebrospinal fluid profiles, and echocardiogram findings were consistent with these diagnoses. Both patients were treated with intravenous immunoglobulin (IVIG) in an intensive care unit (ICU) setting. Echocardiogram findings were reversible. TCM should be recognized as a potential complication of GBS in patients with dysautonomia. This case series adds to the sparse body of literature describing the association between these two conditions. It is not clear if patients with axonal variants of GBS are more predisposed to developing TCM; further, larger case series in the future may help identify the risk factors associated with it. We hope to shed more light on this possible association to expedite the diagnosis and management of this condition.

摘要

吉兰-巴雷综合征(GBS)是一种炎症性多发性神经病,典型表现为腰痛、感觉异常和快速进展的肌无力。GBS患者可出现自主神经功能障碍,而Takotsubo心肌病(TCM)是这种自主神经功能障碍的一种罕见潜在表现。迄今为止,这种关联在文献中仅被报道过12次,我们在此对其进行综述。我们报告两例GBS合并TCM的病例,以提高对这种共病关系的认识,这将促使及时启动适当的支持性治疗,以避免发病和死亡。我们报告了两名患者的病例——一名58岁男性和一名79岁女性——他们在GBS轴索性变体的情况下发生了TCM。电诊断结果、脑脊液检查结果和超声心动图检查结果均与这些诊断相符。两名患者均在重症监护病房(ICU)接受了静脉注射免疫球蛋白(IVIG)治疗。超声心动图检查结果是可逆的。对于自主神经功能障碍的GBS患者,TCM应被视为一种潜在并发症。本病例系列补充了描述这两种疾病之间关联的稀少文献。目前尚不清楚GBS轴索性变体患者是否更易发生TCM;此外,未来更大规模的病例系列可能有助于确定与之相关的危险因素。我们希望能进一步阐明这种可能的关联,以加快对该疾病的诊断和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac1/8324066/93598dd62765/cureus-0013-00000016069-i01.jpg

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