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Autoimmune polyglandular syndrome type II with co-manifestation of Addison's and Graves' disease in a 15-year-old boy: case report and literature review.15 岁男孩中同时出现 Addison 病和 Graves 病的 II 型自身免疫性多腺体综合征:病例报告及文献复习。
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2
13. Children and Adolescents: .儿童和青少年: 。
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3
The neurological syndromes associated with glutamic acid decarboxylase antibodies.与谷氨酸脱羧酶抗体相关的神经综合征。
J Autoimmun. 2019 Jul;101:35-47. doi: 10.1016/j.jaut.2019.04.007. Epub 2019 Apr 15.
4
Autoimmune Polyendocrine Syndromes.自身免疫性多内分泌综合征
N Engl J Med. 2018 Mar 22;378(12):1132-1141. doi: 10.1056/NEJMra1713301.
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Incidence, prevalence and seasonal onset variation of Addison's disease among persons with type 1 diabetes mellitus: nationwide, matched cohort studies.1型糖尿病患者中艾迪生病的发病率、患病率及季节性发病变化:全国性匹配队列研究
Eur J Endocrinol. 2018 Jan;178(1):113-120. doi: 10.1530/EJE-17-0751. Epub 2017 Oct 24.
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2016 Guidelines for the management of thyroid storm from The Japan Thyroid Association and Japan Endocrine Society (First edition).日本甲状腺协会和日本内分泌学会发布的《2016年甲状腺危象管理指南》(第一版)。
Endocr J. 2016 Dec 30;63(12):1025-1064. doi: 10.1507/endocrj.EJ16-0336. Epub 2016 Oct 15.
7
Addison's disease with polyglandular autoimmunity carries a more than 2·5-fold risk for adrenal crises: German Health insurance data 2010-2013.伴有多腺体自身免疫的艾迪生病发生肾上腺危象的风险增加超过2.5倍:2010 - 2013年德国医疗保险数据
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青少年同时患有艾迪生病和格雷夫斯病,出现严重多系统器官功能障碍。

Severe multisystem organ dysfunction in an adolescent with simultaneous presentation of Addison's and Graves' disease.

机构信息

Department of Pediatrics, Golisano Children's Hospital, University of Rochester Medical Center, RochesterNY, USA.

出版信息

J Pediatr Endocrinol Metab. 2020 Dec 15;34(3):411-415. doi: 10.1515/jpem-2020-0438. Print 2021 Mar 26.

DOI:10.1515/jpem-2020-0438
PMID:33675209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8366912/
Abstract

OBJECTIVES

To report an unusual case of simultaneous presentation of Addison's and Graves' disease in an adolescent female previously diagnosed with type 1 diabetes (T1D) and Hashimoto's.

CASE PRESENTATION

A 15-year-old female with T1D and hypothyroidism presented to the emergency department with altered mental state, fever, and left arm weakness for one day. Clinical work-up revealed coexistent new-onset adrenal insufficiency and hyperthyroidism. Her clinical course was complicated by severe, life-threating multisystem organ dysfunction including neurologic deficits, acute kidney injury, and fluid overload. Thyroidectomy was ultimately performed in the setting of persistent signs of adrenal crises and resulted in rapid clinical improvement.

CONCLUSIONS

Endocrinopathy should be included in the differential diagnosis of altered mental status. This case additionally illustrates the challenges of managing adrenal insufficiency in the setting of hyperthyroidism and supports the use of thyroidectomy in this situation.

摘要

目的

报告 1 例罕见病例,患者为既往诊断为 1 型糖尿病(T1D)和桥本甲状腺炎的青少年女性,同时患有艾迪生病和格雷夫斯病。

病例介绍

一名 15 岁女性,患有 T1D 和甲状腺功能减退症,因精神状态改变、发热和左臂无力 1 天就诊于急诊。临床检查发现新出现的肾上腺皮质功能不全和甲状腺功能亢进症同时存在。她的临床病程复杂,伴有严重的危及生命的多系统器官功能障碍,包括神经功能缺损、急性肾损伤和液体超负荷。在持续存在肾上腺危象迹象的情况下,最终进行了甲状腺切除术,导致临床迅速改善。

结论

内分泌疾病应纳入精神状态改变的鉴别诊断。本病例还说明了在甲状腺功能亢进症中管理肾上腺皮质功能不全的挑战,并支持在这种情况下使用甲状腺切除术。