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Neuroschistosomiasis

机译:神经血吸虫病

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摘要

Schistosomiasis (bilharzia) is a neglected tropical disease caused by digenetic trematode platyhelminths of the genus Schistosoma. Neuroschistosomiasis is one of the most severe clinical outcomes associated with schistosome infection. Neurological complications early during the course of infection are thought to occur through in situ egg deposition following aberrant migration of adult worms to the brain or spinal cord. The presence of eggs in the CNS induces a cell-mediated Th2-driven periovular granulomatous reaction. The mass effect of thousands of eggs and the large granulomas concentrated within the brain or spinal cord explain the signs and symptoms of increased intracranial pressure, myelopathy, radiculopathy and subsequent clinical sequelae. Myelopathy (acute transverse myelitis and subacute myeloradiculopathy) of the lumbosacral region is the most common neurological manifestation of S. mansoni or S. haematobium infection, whereas acute encephalitis of the cortex, subcortical white matter, basal ganglia or internal capsule is typical of S. japonicum infection. Cerebral complications include encephalopathy with headache, visual impairment, delirium, seizures, motor deficits and ataxia, whereas spinal symptoms include lumbar pain, lower limb radicular pain, muscle weakness, sensory loss and bladder dysfunction. The finding of eggs in the stool or a positive serology, provides supportive but not direct evidence of neuroschistosomiasis. A definitive diagnosis can only be made with histopathological study showing Schistosoma eggs and granulomas. Schistosomicidal drugs (notably praziquantel), steroids and surgery are currently used for the treatment of neuroschistosomiasis. During the ‘acute phase’ of the disease, neuroschistosomiasis is treated with corticosteroids which are augmented with a course of praziquantel once female worm ovipositioning commences. Surgery should be reserved for special cases such as in those with evidence of medullary compression and in those who deteriorate despite clinical management.
机译:血吸虫病(bilharzia)是一种由血吸虫属的双基因吸虫性蠕虫引起的被忽视的热带病。神经性血吸虫病是与血吸虫感染有关的最严重的临床结局之一。人们认为,在感染过程的早期,神经系统并发症是通过成虫蠕虫向大脑或脊髓异常迁移后原位卵沉积而发生的。中枢神经系统中鸡蛋的存在会诱导细胞介导的Th2驱动的卵巢周肉芽肿反应。数以千计的卵和集中在大脑或脊髓内的大型肉芽肿的质量效应解释了颅内压升高,脊髓病,神经根病和随后的临床后遗症的体征和症状。腰s部区域的脊髓病变(急性横贯性脊髓炎和亚急性脊髓神经根病变)是曼氏沙门氏菌或嗜血链球菌感染的最常见神经系统表现,而皮层,皮层下白质,基底神经节或内囊的急性脑炎是典型的沙门氏菌。日本血吸虫感染。脑并发症包括头痛,视力障碍,del妄,癫痫发作,运动障碍和共济失调的脑病,而脊柱症状包括腰痛,下肢神经根痛,肌肉无力,感觉丧失和膀胱功能障碍。在粪便中发现卵或血清学阳性,可提供神经血吸虫病的支持性证据,但不能直接提供证据。只有通过显示血吸虫卵和肉芽肿的组织病理学研究才能做出明确的诊断。目前使用血吸虫药(尤其是吡喹酮),类固醇和手术治疗神经血吸虫病。在该病的“急性期”,使用女性激素开始产卵后,用皮质类固醇激素治疗神经性血吸虫病。对于特殊情况,应保留外科手术,例如有髓样压迫的证据和尽管经过临床处理却恶化的病人。

著录项

  • 来源
    《Journal of Neurology》 |2012年第1期|p.22-32|共11页
  • 作者单位

    School of Public Health, Griffith University, Meadowbrook, QLD, Australia;

    Molecular Parasitology Laboratory, Infectious Diseases Division, Queensland Institute of Medical Research, Herston, Brisbane, QLD, Australia;

    Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam;

    Division of Pediatric Neurology, Department of Pediatrics, University of Saskatchewan, Saskatoon, Canada;

    Griffith Health Institute, Griffith University, Southport, QLD, Australia;

    Molecular Parasitology Laboratory, Infectious Diseases Division, Queensland Institute of Medical Research, Herston, Brisbane, QLD, Australia;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Schistosomiasis; Bilharzia; Neuroschistosomiasis; Praziquantel;

    机译:血吸虫病;Bilharzia;神经血吸虫病;Praziquantel;

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