僵人综合征和脆性 1 型糖尿病。两个病例的报告

Ismael A. Quintal-Medina MD , Francisco J. Gómez-Pérez MD , Paloma Almeda-Valdes MD, PhD
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引用次数: 0

摘要

背景/目的僵硬综合征(SPS)和1型糖尿病(T1D)是以谷氨酸脱羧酶(GAD)抗体(Abs)为特征的异质性疾病。病例报告我们描述了2例患有T1D和自身免疫性甲状腺疾病的患者,他们表现为肌肉僵硬和间歇性痉挛,影响步态,循环中抗GAD滴度升高。他们分别被诊断为典型的 SPS 和僵硬肢体综合征。通过免疫疗法和肌肉松弛剂,两名患者的肌肉痉挛都得到了缓解,其中一名患者在没有辅助设备的情况下恢复了行走能力。患者还患有血糖变异性高的脆性糖尿病,需要分别使用胰岛素泵和第二代基础胰岛素类似物进行闪光血糖监测。临床异质性意味着γ-氨基丁酸能神经元和胰岛β细胞对抗GAD或其他自身抗体的易感性各不相同。
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Stiff Person Syndrome and Brittle Type 1 Diabetes: Report of 2 Cases

Background/Objective

Stiff person syndrome (SPS) and type 1 diabetes (T1D) are heterogeneous disorders characterized by antibodies (Abs) against glutamic acid decarboxylase (GAD).

Case Report

We describe 2 patients with T1D and autoimmune thyroid disease who presented with muscle rigidity and intermittent spasms that affected gait and with elevated circulating anti-GAD titers. Classic SPS and stiff limb syndrome were diagnosed, respectively. Muscle spasms resolved with immunotherapy and muscle relaxants in both patients, and the ability to ambulate without an assistive device was restored in 1 patient. Patients also had brittle diabetes with high glycemic variability, requiring the use of flash glucose monitoring with an insulin pump and a second-generation basal insulin analog, respectively.

Discussion

GAD Ab–associated syndromes include SPS, T1D, and other endocrinopathies. The clinical heterogeneity implies variable susceptibility of γ-aminobutyric acid-ergic neurons and pancreatic beta cells to anti-GAD or other autoantibodies.

Conclusion

Our case series represent the heterogeneity in natural history, clinical course, and response to therapy in patients with Abs against GAD-spectrum disorders.

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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
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