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本文引用的文献

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Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT): Characteristics, treatment and outcome in 251 cases from the literature.类固醇反应性脑病伴发自身免疫性甲状腺炎(SREAT):文献 251 例特征、治疗和预后。
Autoimmun Rev. 2016 Dec;15(12):1129-1133. doi: 10.1016/j.autrev.2016.09.008. Epub 2016 Sep 15.
2
Hashimoto encephalopathy: A study of the clinical profile, radiological and electrophysiological correlation in a Tertiary Care Center in South India.桥本脑病:印度南部一家三级医疗中心的临床特征、影像学及电生理相关性研究
J Neurosci Rural Pract. 2015 Jul-Sep;6(3):309-14. doi: 10.4103/0976-3147.158753.
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Steroid-Responsive Epilepsia Partialis Continua with Anti-Thyroid Antibodies: A Spectrum of Hashimoto's Encephalopathy?伴有抗甲状腺抗体的类固醇反应性部分性持续性癫痫:桥本脑病的一种表现形式?
Case Rep Neurol. 2014 May 17;6(2):166-70. doi: 10.1159/000363178. eCollection 2014 May.
4
Autoimmune encephalopathy in Graves' disease: remission after total thyroidectomy.格雷夫斯病中的自身免疫性脑病:全甲状腺切除术后缓解
J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):698-9. doi: 10.1136/jnnp.2008.152413.
5
Thyrotoxic autoimmune encephalopathy in a female patient: only partial response to typical immunosuppressant treatment and remission after thyroidectomy.一名女性患者的甲状腺毒症性自身免疫性脑病:对典型免疫抑制治疗仅部分缓解,甲状腺切除术后缓解
Clin Neurol Neurosurg. 2007 Jun;109(5):458-62. doi: 10.1016/j.clineuro.2007.02.006. Epub 2007 Mar 28.
6
Psychiatric presentation of Hashimoto's encephalopathy.桥本脑病的精神症状表现
Psychosom Med. 2007 Feb-Mar;69(2):200-1. doi: 10.1097/PSY.0b013e31803174c0.
7
Steroid-responsive encephalopathy associated with autoimmune thyroiditis.自身免疫性甲状腺炎相关性类固醇反应性脑病
Arch Neurol. 2006 Feb;63(2):197-202. doi: 10.1001/archneur.63.2.197.
8
Manifestation of Hashimoto's encephalopathy years before onset of thyroid disease.桥本脑病在甲状腺疾病发病前数年的表现。
Eur Neurol. 1999;41(2):79-84. doi: 10.1159/000008007.
9
Encephalopathy associated with Hashimoto thyroiditis: diagnosis and treatment.桥本甲状腺炎相关脑病:诊断与治疗
J Neurol. 1996 Aug;243(8):585-93. doi: 10.1007/BF00900946.

格雷夫斯病手术后治疗的脑病

ENCEPHALOPATHY TREATED AFTER SURGERY FOR GRAVES' DISEASE.

作者信息

El Ibrashy I N, El Haddad H M, ElMeligi A M, Radwan M M, Mahgoub K A, Mohsen A A, Abdo R F, Galal M

机构信息

Dept. of Internal Medicine, "Kasr Alainy" Cairo University, Faculty of Medicine, Cairo, Egypt.

Dept. of Occupational and Environmental Medicine, "Kasr Alainy" Cairo University, Faculty of Medicine, Cairo, Egypt.

出版信息

Acta Endocrinol (Buchar). 2022 Jan-Mar;18(1):102-105. doi: 10.4183/aeb.2022.102.

DOI:10.4183/aeb.2022.102
PMID:35975260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9365418/
Abstract

INTRODUCTION

This case report is the fourth of its type in the medical literature. It describes total thyroidectomy for recurrent relapses of Graves encephalopathy (GE) despite medical treatment.

CASE PRESENTATION

A 33-year-old male presented with impaired consciousness and convulsions. He had post-thyroid surgery recurrent Graves' disease with a goitre. Based on this fact, high thyroid antibodies titres and the exclusion of other causes of such neurological manifestations, he was diagnosed to have GE. This is a rare variant of "encephalopathy associated with autoimmune thyroid disease" (EAATD). Despite the administration of steroid therapy and other standard therapeutic measures, he developed five relapses within 17 months. Total thyroidectomy was advised. Unfortunately, he got another severe attack that required intensive care admission. After three days of discharging, he had urgent total thyroidectomy. The operation went well and for 18 months' follow-up he had no more attacks. However, thyroid antibodies remained high.

DISCUSSION

The report provides details on the diagnosis, standard management and the indication for thyroidectomy for GE. It describes its challenges, precautions, technique and outcomes. It reviews the extent of surgery as well as the clinical and antibody outcomes of the previous three related reports, in comparison with the current one.

CONCLUSION

For medically uncontrolled relapse of GE, thyroidectomy consistently results in ending the attacks. It, therefore, should be put in more consideration in the treatment protocols. On the other hand, one should not depend on antibody levels as a measure of treatment success.

摘要

引言

本病例报告是医学文献中此类报告的第四例。它描述了尽管进行了药物治疗,但格雷夫斯脑病(GE)复发后行全甲状腺切除术的情况。

病例介绍

一名33岁男性出现意识障碍和抽搐。他曾接受甲状腺手术后复发性格雷夫斯病并伴有甲状腺肿。基于这一事实、高甲状腺抗体滴度以及排除其他导致此类神经表现的原因,他被诊断为患有GE。这是“自身免疫性甲状腺疾病相关脑病”(EAATD)的一种罕见变体。尽管给予了类固醇治疗和其他标准治疗措施,但他在17个月内复发了5次。建议行全甲状腺切除术。不幸的是,他又一次严重发作,需要入住重症监护病房。出院三天后,他紧急接受了全甲状腺切除术。手术进展顺利,在18个月的随访中他没有再发作。然而,甲状腺抗体仍居高不下。

讨论

该报告提供了关于GE的诊断、标准管理及甲状腺切除术指征的详细信息。它描述了其挑战、预防措施、技术及结果。与当前报告相比,它回顾了手术范围以及前三份相关报告的临床和抗体结果。

结论

对于药物治疗无法控制的GE复发,甲状腺切除术始终能终止发作。因此,在治疗方案中应更多地考虑这一方法。另一方面,不应将抗体水平作为治疗成功的衡量标准。