格雷夫斯病患者发生吉兰-巴雷综合征。

Guillain-Barré Syndrome developing in a patient with Graves' Disease.

作者信息

Majumder Anirban, Basu Sagar

机构信息

Endocrinology Department, KPC Medical College, West Bengal University of Health Sciences, Kolkata, India.

Neurology Department, KPC Medical College, West Bengal University of Health Sciences, Kolkata, India.

出版信息

J ASEAN Fed Endocr Soc. 2019;34(1):103-106. doi: 10.15605/jafes.034.01.17. Epub 2019 May 23.

DOI:10.15605/jafes.034.01.17

PMID:33442145

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7784229/

Abstract

Graves' disease (GD) and Guillain-Barré syndrome (GBS) are both autoimmune disorders and are triggered by interactions between genetic and environmental factors. GBS in patients who suffer from other autoimmune diseases is rarely reported, and the development of atypical GBS with cranial nerve involvement in a patient with GD has never been previously reported. Herein, we report a patient with GD and a rare form of pharyngo-cervico-brachial variety of GBS.

摘要

格雷夫斯病（GD）和吉兰-巴雷综合征（GBS）均为自身免疫性疾病，由遗传因素和环境因素相互作用引发。其他自身免疫性疾病患者并发GBS的情况鲜有报道，而GD患者并发累及颅神经的非典型GBS此前从未有过报道。在此，我们报告1例患有GD且伴有罕见的咽-颈-臂型GBS的患者。