放射治疗综合征后早发性卒中样偏头痛:1例报告及文献复习。

IF 1.9 4区 医学 Q3 CLINICAL NEUROLOGY Journal of Clinical Neuroscience Pub Date : 2025-02-01 DOI:10.1016/j.jocn.2024.110983
Ariana Chow , Gabrielle E.A. Hovis , Farinaz Ghodrati , Maya Harary , Khashayar Mozaffari , Anjali Pradhan , John Hegde , Isaac Yang
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引用次数: 0

摘要

目的:放射治疗后中风样偏头痛发作(SMART)综合征的特征是脑部照射后出现偏头痛、癫痫发作和中风样症状。诊断包括临床症状、脑部照射史和放射学评估。不同患者的发病潜伏期差异很大,从 1 年到 35 年不等。在此,我们回顾了相关文献,并介绍了一例在立体定向放射手术治疗良性脑膜瘤后五个月发病的 SMART 综合征患者:方法:根据 PRISMA 指南对文献进行了系统回顾。我们在 PubMed、Cochrane 和 Web of Science 数据库中搜索了 SMART 综合征病例,并报告了发病时间和放射剂量。最后,我们报告了一名 48 岁女性疑似 SMART 综合征患者的表现、病史、放射学检查结果和临床疗效:结果:在查阅的 101 篇文章中,有 23 篇文章被选入本研究。共发现 27 个病例。患者的平均发病年龄为 43 岁(范围:11-70 岁),71.4% 的患者为男性。平均发病潜伏期为辐射后 11.2 年。根据病例描述,所有患者均未明确接受单次放射外科治疗:结论:SMART 综合征的发病潜伏期、放射剂量、治疗效果和临床过程可能存在差异。本例 SMART 综合征突显了这种疾病临床表现的多样性。应考虑进一步开展工作,以更好地确定诊断 SMART 综合征的临床和放射学标准是否足以涵盖非传统表现的患者。
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Early-onset stroke-like migraine attacks after radiation therapy syndrome: A case report and review of the literature

Purpose

Stroke-like migraine attacks after radiation therapy (SMART) syndrome is characterized by migraines, seizures, and stroke-like symptoms following brain irradiation. Diagnosis consists of clinical signs, history of brain irradiation, and radiographic evaluation. The latency to onset varies widely among individual patients, ranging from 1 to 35 years. Herein, we review the literature and present a case of SMART syndrome with an onset of five months after stereotactic radiosurgery for a benign meningioma.

Methods

A systematic review of the literature was conducted in line with the PRISMA guidelines. The PubMed, Cochrane, and Web of Science databases were searched for cases of SMART syndrome with reported time of onset and radiation dosage. Finally, we report the presentation, history, radiographic findings, and clinical outcomes of a 48-year-old female with suspected SMART syndrome.

Results

Of 101 articles reviewed, 23 articles were selected for inclusion in the present study. A total of 27 cases were identified. The mean age at presentation was 43 years (range: 11–70), and 71.4 % of patients were male. The mean latency to onset was 11.2 years after radiation. Based on case descriptions, none of the patients were definitively treated with single fraction radiosurgery.

Conclusion

SMART syndrome may present with variations in latency to onset, radiation dose, outcome, and clinical course. The present case of SMART syndrome highlights the variety in clinical presentation of this disease. Further work should be considered to better determine whether clinical and radiographic criteria for diagnosing SMART syndrome diagnosis are sufficient to encompass patients with a non-traditional presentation.
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来源期刊
Journal of Clinical Neuroscience
Journal of Clinical Neuroscience 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
402
审稿时长
40 days
期刊介绍: This International journal, Journal of Clinical Neuroscience, publishes articles on clinical neurosurgery and neurology and the related neurosciences such as neuro-pathology, neuro-radiology, neuro-ophthalmology and neuro-physiology. The journal has a broad International perspective, and emphasises the advances occurring in Asia, the Pacific Rim region, Europe and North America. The Journal acts as a focus for publication of major clinical and laboratory research, as well as publishing solicited manuscripts on specific subjects from experts, case reports and other information of interest to clinicians working in the clinical neurosciences.
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