Kostić Aleksandar, Vidović Nataša, Miladinović-Tasić Nataša, Kostić Jovana, Nikolov Vesna, Stojanović Nebojša, Pavlović Miljana
Clinic for Neurosurgery, Clinical Center Niš, Faculty of Medicine, University of Niš, Niš, Serbia.
Institute for Pathology, Clinical Center Niš, Faculty of Medicine, University of Niš, Niš, Serbia.
J Infect Dev Ctries. 2019 Jan 31;13(1):87-92. doi: 10.3855/jidc.10176.
Neurocysticercosis is the most common parasitic disease of the nervous system, nevertheless, it can remain undetected for a long period of time, especially if it occurs in non endemic areas and regions with low-endemicity. Inadequate diagnostic procedures and lack of clinician's dedication towards this health issue can lead to a missed diagnose. Herein, we present a case of a 51-year-old male, with a missed diagnosis of neurocysticercosis for more than two decades. A history of epilepsy had started twenty-one years earlier and was of unclear etiology. Recently, after neurological worsening and headaches, brain computed tomography and magnet resonance imaging was performed as well as Western blot immunoassay of serum and cerebrospinal fluid, surgery, and pathohistological examination of the extracted cysts. Neurocysticercosis was confirmed. Combined therapy that consisted of albendazole and prednisolone was administered for a period of four weeks. Also, antiepileptic therapy was continued. Both clinical status and brain imaging showed the apparent improvement in the patient's condition. Review of the literature was implemented in the discussion that deals with proper and adequate therapy option and outcome factors in neurocysticercosis patients. Over a long period of time, the majority of patients develop seizures as the most common symptom, which requires the administration of medications. Proper diagnostic procedures and adequate combination of surgery and conservative treatment areessential.
神经囊尾蚴病是最常见的神经系统寄生虫病,然而,它可能长期未被发现,尤其是在非流行地区和低流行地区。诊断程序不完善以及临床医生对这一健康问题缺乏关注可能导致漏诊。在此,我们报告一例51岁男性病例,其神经囊尾蚴病漏诊长达二十多年。癫痫病史始于21年前,病因不明。最近,在神经功能恶化和头痛后,进行了脑部计算机断层扫描和磁共振成像,以及血清和脑脊液的免疫印迹检测、手术和对取出囊肿的病理组织学检查。神经囊尾蚴病得到确诊。给予阿苯达唑和泼尼松龙联合治疗四周。同时,继续进行抗癫痫治疗。临床状况和脑部影像学检查均显示患者病情明显改善。在讨论中对文献进行了回顾,内容涉及神经囊尾蚴病患者的恰当和充分治疗方案及预后因素。在很长一段时间内,大多数患者会出现癫痫发作这一最常见症状,这需要用药治疗。恰当的诊断程序以及手术与保守治疗的充分结合至关重要。