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Stiff person syndrome presenting with sudden onset of shortness of breath and difficulty moving the right arm: a case report

机译:僵人综合症,表现为呼吸急促和右臂移动困难突然发作:一例报告

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Introduction First described in 1956, stiff person syndrome is characterized by episodes of slowly progressive stiffness and rigidity in both the paraspinal and limb muscles. Although considered a rare disorder, stiff person syndrome is likely to be under-diagnosed due to a general lack of awareness of the disease in the medical community. Case presentation A 27-year-old Hispanic woman presented to our emergency department with a sudden onset of shortness of breath and difficulty moving her right arm. Her physical examination was remarkable in that her abdomen was firm to palpation and her right upper extremity was rigid on passive and active ranges of motion. Her right fingers were clenched in a fist. Her electromyography findings were consistent with stiff person syndrome in the right clinical setting. Stiff person syndrome is confirmed by testing for the anti-glutamic acid decarboxylase antibody. Her test for this was positive. Conclusion Stiff person syndrome may not be a common condition. However, if disregarded in the differential diagnosis, it can lead to several unnecessary tests being carried out causing a delay in treatment. This case report reveals some of the characteristic features of stiff person syndrome with an atypical presentation.
机译:简介僵硬人综合症于1956年首次被描述,其特征是脊柱旁和四肢肌肉均逐渐出现僵硬和僵硬。尽管僵直人综合症被认为是一种罕见的疾病,但由于医学界普遍缺乏对该疾病的认识,因此可能未得到充分诊断。病例介绍一名27岁的西班牙裔妇女突然出现呼吸急促,右臂移动困难,出现在我们的急诊室。她的身体检查非常出色,腹部紧实,触及的上肢在被动和主动运动范围内都僵硬。她的右手指握紧拳头。她的肌电图检查结果与正确的临床环境中的僵硬人综合征相符。通过测试抗谷氨酸脱羧酶抗体可以确认僵人综合症。她对此的测试是积极的。结论僵硬的人综合征可能不是普遍的情况。但是,如果在鉴别诊断中将其忽略,则可能导致进行一些不必要的测试,从而导致治疗延迟。该病例报告通过非典型表现揭示了僵硬人综合症的一些特征。

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