【以难治性恶心、呕吐、呃逆为表现的视神经脊髓炎谱系障碍区后综合征的临床特点及误诊分析】。

S M Zhang, F Qiu, X Sun, H Sun, L Wu, D H Huang, W P Wu
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引用次数: 0

摘要

目的:探讨神经脊髓炎视谱病(NMOSD)中以难治性恶心、呕吐、呃嗝为表现的区域后发综合征(APS)的误诊情况,降低误诊风险。方法:回顾性分析2019年1月至2021年7月在解放军总医院第一医疗中心神经内科就诊的NMOSD患者的资料。应用SPSS25.0分析APS的表现、误诊和误治。结果:共纳入NMOSD患者207例,其中男性21例,女性186例。平均发病年龄39±15岁(5 ~ 72岁)。血清水通道蛋白4抗体阳性比例为82.6%(171/207)。总体而言,35.7%(74/207)的NMOSD患者在病程中出现APS;其中70.3%(52/74)的患者以APS为首发症状,29.7%(22/74)的患者以APS为继发症状。误诊率分别为90.4%(47/52)和50.0%(11/22)。作为首发症状,19.2%(10/52)的患者在APS期间仅表现为难治性恶心、呕吐和呃逆;80.8%(42/52)的患者出现其他神经系统症状。首诊APS最多的科室为消化内科和普通内科,分别占54.1%和17.6%。最常见的误诊与消化系统疾病有关,误诊的中位时间为37天。结论:APS是NMOSD的常见症状,误诊率高。APS常伴有其他伴随症状。如果我们要减少和避免误诊,提高对这种疾病/综合征的认识,获得详细的患者病史,并进行体检是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of the clinical characteristics and misdiagnosis of area postrema syndrome manifesting as intractable nausea, vomiting, and hiccups in neuromyelitis optica spectrum disorders].

Objective: To investigate the misdiagnosis of area postrema syndrome (APS) manifesting as intractable nausea, vomiting and hiccups in neuromyelitis optic spectrum disease (NMOSD) and reduce the risk of misdiagnosis. Methods: We retrospectively analyzed data from NMOSD patients attending the Department of Neurology at the First Medical Center of PLA General Hospital between January 2019 and July 2021. SPSS25.0 was then used to analyze the manifestations, misdiagnosis, and mistreatment of APS. Results: A total of 207 patients with NMOSD were included, including 21 males and 186 females. The mean age of onset was 39±15 years (range: 5-72 years). The proportion of patients who were positive for serum aquaporin 4 antibody was 82.6% (171/207). In total, 35.7% (74/207) of the NMOSD patients experienced APS during the disease course; of these patients, 70.3% (52/74) had APS as the first symptom and 29.7% (22/74) had APS as a secondary symptom. The misdiagnosis rates for these conditions were 90.4% (47/52) and 50.0% (11/22), respectively. As the first symptom, 19.2% (10/52) of patients during APS presented only with intractable nausea, vomiting and hiccups; 80.8% (42/52) of patients experienced other neurological symptoms. The Departments of Gastroenterology and General Medicine were the departments that most frequently made the first diagnosis of APS, accounting for 54.1% and 17.6% of patients, respectively. The most common misdiagnoses related to diseases of the digestive system and the median duration of misdiagnosis was 37 days. Conclusions: APS is a common symptom of NMOSD and is associated with a high rate of misdiagnosis. Other concomitant symptoms often occur with APS. Gaining an increased awareness of this disease/syndrome, obtaining a detailed patient history, and performing physical examinations are essential if we are to reduce and avoid misdiagnosis.

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