Suppr超能文献

克罗恩病与抗谷氨酸脱羧酶(GAD)相关自身免疫性脑炎并存:一例报告

Concomitant Crohn's Disease and Anti-Glutamic Acid Decarboxylase (GAD)-Associated Autoimmune Encephalitis: A Case Report.

作者信息

Akkoyun Erkam, Akyuz Filiz, Cavus Bilger, Gunduz Tuncay, Kürtüncü Murat

机构信息

Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, TUR.

Department of Gastroenterology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, TUR.

出版信息

Cureus. 2023 Sep 16;15(9):e45344. doi: 10.7759/cureus.45344. eCollection 2023 Sep.

Abstract

Crohn's disease is an inflammatory, autoimmune disorder that predominantly affects the intestines but can also affect extraintestinal organs. Certain neurological conditions, such as autoimmune encephalitis, can develop along with this disease. In this case report, we present a case of anti-glutamic acid decarboxylase (GAD) antibody-associated autoimmune encephalitis that occurred shortly after the diagnosis of Crohn's disease and was unrelated to the treatment and nutritional deficiencies. After a significant weight loss (24 kg) and persistent diarrhea, the patient was diagnosed with Crohn's disease by colonoscopy and biopsy. Within two weeks after the diagnosis, he experienced altered consciousness and memory impairment, followed by a rapid deterioration in consciousness and respiratory distress, leading to intubation and admission to the intensive care unit. His brain MRI revealed asymmetrical diffuse cortical diffusion restrictions, hyperintense signals on fluid-attenuated inversion recovery (FLAIR) sequences, and diffuse pachymeningeal contrast enhancement involving both cingulate gyri, bilateral insular cortices, amygdalae, hippocampi, and the right precuneus. Analysis of cerebrospinal fluid (CSF) revealed a slight elevation of CSF proteins, and the patient tested positive for serum anti-GAD antibodies. The patient responded favorably to a seven-day course of intravenous methylprednisolone, five days of intravenous immunoglobulin (IVIG), and oral corticosteroids. Subsequent treatment consisted of monthly IVIG, azathioprine, and vedolizumab, resulting in no neurologic sequelae except mild amnesia. A follow-up MRI at three months showed a nearly complete disappearance of the lesions. This is the first reported case of anti-GAD-associated encephalitis occurring in the presence of Crohn's disease.

摘要

克罗恩病是一种炎症性自身免疫性疾病,主要影响肠道,但也可累及肠道外器官。某些神经系统疾病,如自身免疫性脑炎,可与这种疾病同时发生。在本病例报告中,我们介绍了一例抗谷氨酸脱羧酶(GAD)抗体相关的自身免疫性脑炎病例,该病例在克罗恩病诊断后不久发生,与治疗及营养缺乏无关。在体重显著减轻(24千克)和持续腹泻后,患者经结肠镜检查和活检被诊断为克罗恩病。诊断后两周内,他出现意识改变和记忆障碍,随后意识迅速恶化并出现呼吸窘迫,导致插管并入住重症监护病房。他的脑部磁共振成像(MRI)显示不对称性弥漫性皮质扩散受限、液体衰减反转恢复(FLAIR)序列上的高信号,以及累及扣带回、双侧岛叶皮质、杏仁核、海马体和右侧楔前叶的弥漫性硬脑膜强化。脑脊液(CSF)分析显示CSF蛋白略有升高,患者血清抗GAD抗体检测呈阳性。患者对为期七天的静脉注射甲泼尼龙疗程、五天的静脉注射免疫球蛋白(IVIG)和口服糖皮质激素反应良好。后续治疗包括每月一次的IVIG、硫唑嘌呤和维多珠单抗,除轻度失忆外未留下神经后遗症。三个月后的随访MRI显示病变几乎完全消失。这是首例报道的在克罗恩病患者中发生的抗GAD相关脑炎病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e474/10577508/1ae39beffe44/cureus-0015-00000045344-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验