眼科

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58例特发性颅内压增高症早期误诊为眼科疾病之探讨

马中华 江汉秋 王佳伟   

  1. 100730 首都医科大学附属北京同仁医院神经内科
  • 收稿日期:2018-11-13 出版日期:2019-03-25 发布日期:2019-03-28
  • 通讯作者: 王佳伟,Email wangjwcq@163.com
  • 基金资助:

    神经病学(神经免疫学)北京同仁医院院内基金重点医学专业发展计划(trzdyxzy201704)

Misdiagnosis of 58 cases with idiopathic intracranial hypertension as ophthalmic disease

 MA Zhong-hua, JIANG Han-qiu, WANG Jia-wei   

  1. Department of Neurology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
  • Received:2018-11-13 Online:2019-03-25 Published:2019-03-28
  • Contact: WANG Jia-wei, Email: wangjwcq@163.com

摘要:

目的 分析特发性颅内压增高症(idiopathic intracranial hypertension,IIH)误诊为眼科疾病患者的临床特点,总结减少误诊误治的措施,提高临床诊断正确率。设计 回顾性病例系列。研究对象 58例IIH误诊患者。方法 回顾性分析58例依据国际IIH诊断标准明确诊断为IIH、但入院前均误诊为不同眼科疾病患者的临床资料,总结误诊患者特点及误诊原因。主要指标 临床表现、误诊情况、视功能、影像学检查结果、误诊后治疗转归及入院后确诊情况。 结果 58 例误诊患者病程6天~8年,平均7.4个月,其中3个月内者36例(62.1%);临床症状以眼部症状为主(100%),持续性视力下降最多见(36例,62.0%);所有患者均有双侧视乳头水肿;入院前均未接受腰椎穿刺检查。误诊诊断前3位的依次是:视神经炎 32 例(55.2%),前部缺血性视神经病变12例(20.7%),视盘血管炎5例(8.6%);46例患者(79.3%)接受过糖皮质激素治疗,疗效差。腰椎穿刺测颅压均高于25 cmH2O。根据病情给予药物或手术治疗。结论 以视力下降等眼部症状为主要表现的视乳头水肿患者,易误诊为视神经炎或缺血性视神经病变。及时测颅压及头部磁共振等辅助检查,可有效提高临床诊断的正确率。 (眼科,2019, 28: 140-144)

关键词: 特发性颅内压增高症, 误诊, 临床分析

Abstract:

Objective To analyze the clinical characteristics and the causes of misdiagnosis of Idiopathic intracranial hypertension(IIH) to reduce the diagnosis error rate. Design Retrospective case series. Participants 58 patients with IIH misdiagnosed as ophthalmopathy. Methods The clinical data of 58 patients with IIH (according to international of IIH)were analyzed in this retrospective research. These cases were selected from patients hospitalized in Tongren Hospital from January 2014 to December 2017, and were all misdiagnosed as ophthalmopathy before admission. Clinic data were extracted to ascertain the causes of misdiagnosis. Main Outcome Measures Clinical manifestations, misdiagnosis condition, visual function examination, imaging examination, treatment outcome after misdiagnosis and diagnosis after admission. Results 58 cases were under observation, including 22 males (37.9%) and 36 females (62.1%). The duration of disease ranged from 6 days to 8 years, with an average of 7.4 months, including 36 cases (62.1%) within 3 months. The main clinical symptoms were ocular symptoms, while continuous vision loss was the most common (62.0%). The top four misdiagnosis were optic neuritis (ON) in 32 cases (55.2%), anterior ischemic optic neuropathy(AION) in 12 cases (20.7%), papilledema in 6 cases (10.3%) and optic vasculitis in 5 cases(8.6%). 46 patients (79.3%) had received glucocorticosteroid therapy, with poor efficacy. After admission, lumbar puncture was launched and intracranial pressure of all patients was higher than 25 cmH2O. Combined with the medical history, physical signs, and results of brain/orbital imaging examination and laboratory tests, the diagnosis was confirmed as IIH. Medication or surgery may be administered depending on the patient's condition. Conclusions Patients with papilledema who are mainly characterized by decreased vision are easily misdiagnosed as optic neuritis or ischemic optic neuropathy. Timely measurement of intracranial pressure and head magnetic resonance and other auxiliary examinations can effectively improve the accuracy of clinical diagnosis. (Ophthalmol CHN, 2019, 28: 140-144)

Key words: idiopathic intracranial hypertension, misdiagnosis, clinical analysis