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[曼氏血吸虫引起的脑脊膜神经根炎。研究方案及21例报告]

[Meningomyeloradiculitis caused by Schistosoma mansoni. Research protocol and report of 21 cases].

作者信息

Peregrino A J, de Oliveira S P, Porto C A, Santos L A, de Menezes E E, Silva A P, Brito A L, Pinheiro S P, Pinheiro S, Dias A B

机构信息

Grupo de Pesquisas de Neurologia Tropical nas Américas da Federção Mundial de Neurologia, Itabuna, Brasil.

出版信息

Arq Neuropsiquiatr. 1988 Mar;46(1):49-60. doi: 10.1590/s0004-282x1988000100009.

Abstract

Twenty one cases of schistosomal meningomyeloradiculopathy due to Schistosoma mansoni are reported. This result was attained after a 4- year research period based on a "Clinical and Laboratory Investigation Protocol" applied on 212 patients in Itabuna, a city of Southeast region of Bahia state in the Northeast of Brazil. This region is a non endemic one for schistosomiasis. The Protocol consisted in leading to investigation every patient that presented a clinical triad characterized by: lumbar pain, paresthesias in the inferior limbs, miction difficulties. Diagnostic criteria were based on clinical neurologic signs, presence of Schistosoma mansoni eggs on feces or rectum biopsy, positive immunofluorescence reaction for schistosomiasis in the cerebrospinal fluid (CSF), the inflammatory CSF characteristics, and an exhaustive research for differential diagnosis. The diagnosis has been essentially based on clinical and laboratory data, not having for any of the cases an histopathological study. The treatment was performed the earliest as possible, and corticosteroids associated to oxaminiquine were used for all cases. The patients were studied as to sex, age, profession, city of origin, initial symptoms, laboratory tests related to schistosomiasis, the onset type of neurologic clinical symptoms and several CSF aspects. Treatment beginning was related with time of disease. Clinical evolution and sequelae were analysed. Abdominal contractions were observed in 10 cases several hours before the clinical picture had been clearly presented. Clinical diagnosis is justified since it is performed under severe clinical and laboratory evidences, as well as an accurate search for differential diagnosis. The authors think that the schistosomal meningomyeloradiculopathy is a well defined nosological entity by its neurological picture, as also from the pathological point of view. Finally, the authors suggest to neurological services of the country the planning and application of similar or even more detailed Protocol in order to obtain an early diagnosis and treatment for the disease, preventing so irreversible damages and sequelae very harmful for the patients in their social life.

摘要

报告了21例因曼氏血吸虫引起的血吸虫性脊髓脊膜神经根病。这一结果是在对巴西东北部巴伊亚州东南部城市伊塔布纳的212名患者应用“临床与实验室调查方案”进行了4年研究之后得出的。该地区并非血吸虫病流行地区。该方案包括对每一位出现以下临床三联征的患者进行调查:腰痛、下肢感觉异常、排尿困难。诊断标准基于临床神经学体征、粪便或直肠活检中曼氏血吸虫卵的存在、脑脊液(CSF)中血吸虫病免疫荧光反应阳性、脑脊液的炎症特征以及全面的鉴别诊断研究。诊断主要基于临床和实验室数据,所有病例均未进行组织病理学研究。治疗尽早进行,所有病例均使用皮质类固醇联合奥沙米喹。对患者的性别、年龄、职业、原籍城市、初始症状、与血吸虫病相关的实验室检查、神经临床症状的发病类型以及脑脊液的几个方面进行了研究。治疗开始时间与疾病时间相关。分析了临床演变和后遗症。在临床表现清晰出现前数小时,10例患者观察到腹部收缩。临床诊断是合理的,因为它是在严格的临床和实验室证据以及准确的鉴别诊断基础上进行的。作者认为,血吸虫性脊髓脊膜神经根病从神经学表现以及病理学角度来看都是一个明确的病种实体。最后,作者建议该国的神经科服务部门制定并应用类似或更详细的方案,以便对该疾病进行早期诊断和治疗,从而防止对患者社会生活造成极其有害的不可逆转的损害和后遗症。

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